Institute of Oceanology, Chinese Academy of Sciences
Article Information
- SHI Yu, PAN Xiaolan, XU Meng, LIU Huiru, XU Hanzhi, HE Maoxian
- The role of Smad6 in immunity of the pearl oyster Pinctada fucata martensii
- Journal of Oceanology and Limnology, 40(3): 1135-1147
- http://dx.doi.org/10.1007/s00343-021-1088-8
Article History
- Received Mar. 26, 2021
- accepted in principle May. 28, 2021
- accepted for publication Jun. 30, 2021
2 Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou), Guangzhou 511458, China
The transforming growth factor β (TGF-β) family plays crucial roles in embryonic development, differentiation of cells, formation of organs, and adult tissue homeostasis. The family includes TGF-βs, activins, bone morphogenetic proteins (BMPs), and growth and differentiation factors (GDFs). TGF-βs and activins are preferentially phosphorylated by Smad2 and Smad3, whereas BMP signals are preferentially transmitted by Smad1/5/8 (Zhang et al., 1996).
The Smad protein family is an important medium for transducing BMP-Smads signals and includes R-Smads (receptor-regulated Smads, Smad1, 5, 8, 9), Co-Smads (common partner Smads, Smad4), and I-Smads (inhibitory Smads, Smad6, 7). BMPs trigger signaling through binding the transmembrane receptor BMPR-Ⅱ. The formed ligand-receptor complex phosphorylates and activates BMPR-Ⅰ, which has intrinsic serine-threonine kinase activities. The activated BMPR-Ⅰ phosphorylates R-Smads, which then form heterotrimeric complexes with Co-Smads. The formed complexes then translocate to the nucleus to bind to co-activating factors or inhibitory factors to activate or repress gene expression (von Bubnoff and Cho, 2001).
Inhibitory Smads (I-Smads) contain a conserved carboxy-terminal MH2 domain (Goto et al., 2007). Smad6 inhibits BMP2 signaling by a variety of mechanisms, including interaction with activated type I receptors or with activated phosphorylation of Smad1/5 (Ishida et al., 2000; Itoh et al., 2001), and the MH2 domain is required for these interactions. Smad6 can also interact with Smad4 to inhibit BMP2 signaling (Hata et al., 1998). In the nucleus, Smad6 inhibits the BMP signaling pathway by interacting with homeobox C8 (Hoxc8) and Hoxc9 or by binding to the target DNA (Bai et al., 2000; Bai and Cao, 2002). In vertebrates, Smad3 preferentially transfers TGF-β signals, and TGF-β signaling is inhibited by Smad7 (Hanyu et al., 2001). However, Smad7 was not found in mollusc, there was only one inhibitory Smad (Smad6) in mollusc. Therefore, if Smad3 can transfer BMP2 signals and if Smad6 can inhibit BMP2 signaling by interacting with Smad3 in Pinctada fucata martensii needs to be studied. To date, most studies of BMP-Smads signaling pathway-related genes focused on characterization of ligands, receptors, and Smad family members and their involvement in development and shell formation in invertebrates, such as Crassostrea gigas (Herpin et al., 2005; Lelong et al., 2007; Le Quéré et al., 2009; Liu et al., 2014), Lymnaea stagnalis (Iijima et al., 2008; Shimizu et al., 2011), P. f. martensii (Miyashita et al., 2008; Shi et al., 2020), Patella vulgate(Nederbragt et al., 2002), Drosophila(Raftery and Sutherland, 1999), Hydra (Reinhardt et al., 1996), Caenorhabditis elegans (Savage et al., 1996), and various corals (Zoccola et al., 2009). However, little is known about the roles of these genes in molluscan immunity.
Members of the TGF-β superfamily are involved in innate immunity in both vertebrates and invertebrates (Lieber and Luckhart, 2004; Nicholas and Hodgkin, 2004). In vertebrates, I-Smads can mediate the effect of TGF-β on anti-inflammatory activity. Smad6 suppresses innate immunity responses by recruiting Smurfs to MyD88 and triggers its polyubiquitylation and proteasomal degradation to inhibit the MyD88-dependent pathway (Lee et al., 2011). Smad6 also can interfere with the toll-like receptor 4 signaling pathway (Choi et al., 2006). Smad6 methylation represses nuclear factor κB (NF-κB) activation and periodontal inflammation (Zhang et al., 2018). In mollusks, a TGF-b/activin homologue from C. gigas (Lelong et al., 2007), Smad4 of Biomphalaria glabrata (Adema et al., 2010), Smad3 and Smad5 of Hyriopsis cumingii (Hu et al., 2017; Li et al., 2020), and Smads1/5 of P. f. martensii (Shi et al., 2021) were reported to be involved in immunity against bacterial challenge and in wound healing. However, whether Smad6 plays a role in immunity in mollusks is unknown.
The pearl oyster P. f. martensii is mainly cultivated in China and Japan for pearl production. This marine bivalve also is an important model for studying biomineralization, genetic variation, growth, and resistance to disease. The process of artificially inserting an extraneous piece of mantle into the recipient oyster to form a pearl sac can injure the animal and lead to bacterial and viral diseases, which in turn can cause large-scale mortality and enormous economic losses (Miyazaki et al., 1999; Kitamura et al., 2000; Potasman et al., 2002; De Zoysa and Lee, 2009). Thus, it is important to understand the innate immunity of this species to improve culture conditions and pearl production.
In our previous studies, we characterized the BMP2-Smads signals in P. f. martensii and explored the signaling pathway by which Smad1/5 transduces the BMP2 signal to regulate shell formation (Zhao et al., 2016; Shi et al., 2020). We identified Smad6, which regulates BMP2-Smads signaling with a negative feedback in vertebrates. However, whether Smad6 is involved in immunity and whether it plays a similar negative role in P. f. martensii was not known. Therefore, the goals of this study were to phylogenetically analyze the protein sequences of Smad6, examine the mRNA expression of Smad6 in different tissues and developmental stages, characterize the role of Smad6 and Smad3 after immune challenge, and investigate the expression of Smad6 and Smad3 during wound healing. We also assessed the expression of genes involved in BMP2-Smads signaling [BMP2 (AB176952), Smad3 (ABX57736), Smad4 (AGY49100), Smad1/5(AGI96394), Smad6 (AGI96395), and muscle segment homeobox (MSX) (KJ028208)] and immunity [NF-κB (JQ061255), matrix metalloproteinase1 (MMP, KC881251), interleukin 17 (IL-17, JX971444), tissue inhibitor of metalloproteinase (TIMP, KP852352), copper-zinc-superoxide dismutase (CuZn-SOD, PB 4757.2 from the genome of P. f. martensii), and lipopolysaccharide (LPS)-induced tumor necrosis factor α (LITAF, PB 1747.11 from the genome of P. f. martensii)] after oysters were exposed to salinity stress.
2 MATERIAL AND METHOD 2.1 AnimalPinctada fucata martensii (2 years old) were obtained from the Marine Biology Research Station at Daya Bay of the Chinese Academy of Sciences (Shenzhen, Guangdong, China). These oysters were cultivated in the sea and acclimated in floating net cages under natural conditions.All animal experiments were conducted in accordance with the guidelines and approval of the respective Animal Research and Ethics Committees of the Chinese Academy of Sciences (Shi et al., 2020).
2.2 Phylogenetic treeMultiple alignments of the Smad6 amino acid sequences were performed using ClustalW 1.81. Protein phylogenetic analysis was conducted with MEGA (Molecular Evolutionary Genetics Analysis)6.0 using the neighbor-joining method.
2.3 Expression of Smad6 in tissues of P. f.martensiiThe expression pattern of Smad6 mRNA in the tissues of P. f. martensii was analyzed using quantitative real-time PCR (qRT-PCR). Total RNA was isolated from eight tissues (intestines, adductor muscle, foot, mantle, heart, testis, digestive gland, and gill) from three individuals. qRT-PCR was performed on the samples following Shi et al. (2012).Smad6 transcript levels were normalized against 18s transcripts levels, as 18s was expressed equally in all tested tissues. The level of expression was calculated using the 2-ΔΔCt method. Table 1 lists the primers used for qRT-PCR analysis.
2.4 Expression of Smad6 in different developmental stages of P. f. martensiiTo analyze the developmental expression patterns of Smad6 in P. f. martensii, 10 developmental stages (polar body stage, four cell, eight cell, blastula stage, gastrula stage, trochophores, D-shaped larvae, umbo larvae, eyespot larvae, and attached larvae) were collected and stored at -80 ℃. The total RNA extraction and qRT-PCR analyses were performed following Shi et al. (2012) for three replicates of each developmental stage. The mRNA expression of 18s was stable in all tested developmental stages, so it was used to calculate the relative level of Smad6 expression.
2.5 LPS and polyinosinic: polycytidylic (poly (I:C)) challengePinctada fucata martensii were randomly divided into three groups for intramuscular injection with i) 100 μL of LPS (Sigma-Aldrich, St. Louis, MO, USA) dissolved in sterile phosphate-buffered saline (PBS) at a final concentration of 1 μg/μL, ⅱ) 100 μL of poly (I:C) (Invivogen, San Diego, CA, USA) dissolved in sterile PBS at a final concentration of 1 μg/μL, or ⅲ) 100 μL of sterile PBS as the control. After treatment, nine individuals form each group were randomly sampled at 0, 12, 24, 36, 48, and 72 h post injection. Mantle tissues were quickly dissected, frozen in liquid nitrogen, and stored at -80 ℃ for subsequent RNA extraction. Expression of Smad6 and Smad3 mRNA was examined using qRT-PCR as described previously (Shi et al., 2020).
2.6 Wound healing assayThe V-shaped notch experiment was performed according to a previously described method (Shi et al., 2020). The primers used to measure the expression levels of Smad6 and Smad3 are listed in Table 1.
2.7 Salinity stress experimentFor the salinity stress experiment, we soaked five plastic buckets in 10 mg/L of potassium permanganate solution for 10 min, rinsed them, and then filled with 70 L of filtered seawater. Fresh water and salt crystals were mixed to create a salinity gradient of 16, 20, 29, 32, and 36. Because the salinity of seawater in the aquaculture area was 29, 29 was used as the control group. Two hundred P. f. martensii were randomly divided into five groups and placed in the buckets. Five individuals from each group were randomly sampled at 4, 24, 72, 120, and 168 h after treatment. Gill tissues were quickly dissected, frozen in liquid nitrogen, and stored at -80 ℃ for subsequent RNA extraction. BMP2, Smad3, Smad4, Smad1/5, Smad6, MMP, MSX, NF-κB, IL-17, TIMP, CuZn-SOD, and LITAF mRNA expression levels were measured using qRT-PCR, which was performed as described previously (Shi et al., 2020).
2.8 Statistical analysisQuantitative data are shown as the mean ± standard deviation (SD). Figures were constructed using GraphPad Prism 8 (La Jolla, CA, USA). All values were compared by one-way analysis of variance (ANOVA) followed by Duncan's multiple range tests, two-way ANOVA followed by posttests, or a t-test, all performed using SPSS 13.0 (SPSS Inc., Chicago, IL, USA). Differences were considered to be statistically significant at P < 0.05 or P < 0.01.
3 RESULT 3.1 Phylogenetic analysis of the Smad family of P. f. martensiiPhylogenetic analysis showed that the Smad family genes are clustered into five separate clades in P. f. martensii: the Smad1/5/8/9 cluster and Smad2/3 cluster are aggregated into R-Smads, the Smad6 cluster and Smad7 cluster are aggregated into I-Smads, and the Smad4 cluster is aggregated into Co-Smad. Smad5 of P. f. martensii is located in the Smad1/5/8/9 cluster and is most closely related to that of Crassostrea virginica; Smad3 is located in the Smad2/3 cluster and is most closely related to that of C. gigas; Smad4 is located in the Smad4 cluster and is most closely related to that of C. virginica; and Smad6 is located in the Smad6 cluster and is most closely related to that of C. gigas and C. virginica (Fig. 1).
3.2 Tissue distribution of Smad6 in P.f. martensiiThe Smad6 mRNA was expressed in all tissues examined, with the highest level in the gill, a moderate level in adductor muscle, mantle, testis, intestines, and foot, and a low level in the digestive gland and heart (Fig. 2).
3.3 Expression of Smad6 in different developmental stages of P. f. martensiiThe Smad6 mRNAs were expressed at all developmental stages examined. The mRNA levels were moderate in the polar body stage, peaked at the eight-cell stage, decreased to a moderate level from the blastula to the gastrula stage, and then decreased significantly in the trochophore stage. The expression level was low from the D-shaped larva stage to the attached larval stage (Fig. 3).
3.4 Responses of Smad6 and Smad3 in P. f. martensii challenged with LPS and poly (I:C)To determine whether Smad6 and Smad3 in the mantle of P. f. martensii are involved in innate immune defense, their temporal expression patterns were monitored after the oysters were stimulated by LPS and poly (I:C). After LPS stimulation, the mRNA expression of Smad3 significantly increased at 36 h but returned to the original level at 48 and remained there until the end of the experiment; expression was significantly up-regulated at 12 h, peaked at 48 h, and remained high thereafter in the poly (I:C) stimulation group. The mRNA expression of Smad6 was significantly increased at 24 h, remained high until 48 h, and peaked at 72 h after LPS stimulation; expression was significantly up-regulated at 48 h and 72 h after poly (I:C) stimulation (Fig. 4).
3.5 Smad6 and Smad3 mRNA expression during wound healingIn the wound healing experiment, the mRNA expression of Smad3 was significantly down-regulated from 2 to 24 h compared with 0 h, then it dramatically increased at 120 h post wounding. The transcript levels of Smad6 were significantly higher at 24 h and 120 h post wounding compared with 0 h (Fig. 5).
3.6 Expression of genes involved in BMP2-Smads signaling and immunity after exposure to salinity stressThe temporal expression of genes involved in BMP2-Smads signaling and immunity in the gills of P. f. martensii after exposure to salinity stress was evaluated to better understand their role mantle immunity function. The mRNA expression of BMP2, Smad4, Smad1/5, Smad6, MSX, IL-17, TIMP, CuZn-SOD, and LITAF was significantly up-regulated compared to the control (29) during low salinity (16 or/and 20) treatment, whereas the levels of NF-κB and MMP transcripts were significantly decreased. Smad3 expression increased in the 20 salinity treatment at 24 h but then decreased from 72 to 120 h. High salinity treatment (32 or/and 36) resulted in significantly increased expression of BMP2, Smad4, Smad1/5, Smad6, MSX, IL-17, TIMP, CuZn-SOD, and LITAF and decreased expression of Smad3 and NF-κB compared to the control (29) from 4 to 168 h. MMP expression was significantly down-regulated at 4 h and from 72 to 168 h after 32 salinity treatment, but it was higher than the control at 24 h. At 36, expression of MMP decreased at 4 h, peaked at 24 h, remained high until 120 h, and then decreased at 168 h (Fig. 6).
4 DISCUSSIONWe conducted multiple sequence alignment to study the phylogenetic relationships between Smad6 and other members of the Smads family in P. f. martensii and found that five independent branches (Smad1/5/8/9, Smad2/3, Smad4, Smad6, Smad7) are present in the phylogenetic tree. Smad6 is located in the Smad6 cluster and is most closely related to that of C. gigas and C. virginica.
Smad6 was expressed in all tissues examined, showing its wide distribution in the adult body. This pattern indicates that Smad6 has diverse functions in physiological processes of P. f. martensii. Moreover, the highest expression level in the gill and moderate level in the mantle suggest that Smad6 may be involved in immunity of P. f. martensii.
Smad6 mRNA also was expressed in all 10 development stages tested, with high levels in embryonic stages and low levels in the larval stages. This result suggests that Smad6 may play an important role in early development of P. f. martensii. The period from the trochophore stage to D-shaped larvae is very important for metamorphosis in bivalves, and key activities such as cell proliferation and shell formation takes place during this period (Liu et al., 2014). In our study, the mRNA expression of Smad6 decreased beginning at the D-shaped larval stage, which suggests that the inhibitory effect of Smad6 was down-regulated.
The mRNA expression levels of Smad3 and Smad6 were up-regulated in the mantle of P. f. martensii after LPS and poly (I:C) stimulation. These data suggest the potential role of Smad3 and Smad6 in innate immunity to defend against bacterial and viral infections. The mRNA expression of Smad3 was significantly up-regulated 12 h after Poly (I:C) treatment and remained high at 72 h. It also increased 24 h after LPS treatment and remained high until 36 h. These results indicate that Smad3 was more sensitive and more persistent to Poly (I:C) than to LPS stimulation. Hu et al. (2017) reported that HcSmad3 expression in H. cumingii was up-regulated in hemocytes and the hepatopancreas after Aeromonas hydrophila and peptidoglycan stimulation, suggesting that Smad3 may play a role in innate immunity in bivalves. However, Smad6 seemed be more sensitive and more persistent to LPS than to Poly (I:C), suggesting that it may be involved in immunity in a different way from that of Smad3. Additionally, Smad6 seemed to play a positive role after LPS and poly (I:C) challenge in P. f. martensii.
Wound healing is an essential process in which the separated or destroyed tissue attempts to restore itself to its normal state (Mokoena et al., 2018). TGF-β is one of the essential growth factors involved in wound healing, and it is dependent on the Smads pathway. TGF-β activates downstream mediators Smad2 and Smad3, which results in the differentiation of fibroblasts into alpha smooth muscle-expressing myofibroblasts (Xu et al., 2016). In our study, Smad3 expression significantly decreased from 2 to 24 h after wounding, but then increased at 120 h. In contrast, Smad6 expression was significantly up-regulated at 24 and 120 h after wounding. This opposite expression pattern suggests that Smad3 may play a positive role and Smad6 may play a negative role during wound healing. However, whether up-regulated Smad6 expression suppresses Smad3 expression within 24 h of wounding requires further investigation. In H. cumingii, Smad3 expression did not change significantly after wounding, whereas expression of Smad4 and HcSmad5 was significantly up-regulated post wounding (Hu et al., 2017; Li et al., 2020). Biomphalaria glabrata Smad4 and Cgi-SMAD1/5/8 levels were also increased post wounding (Adema et al., 2010; Liu et al., 2014). These results indicate that Smads family members may play a complex role in mollusk immunity.
Most marine bivalves can vary their osmotic pressure. When encountering salinity change, they first respond by closing the shell and sealing the mantle cavity, and then they regulate the expression of genes related to ion exchange and water transport in the body (Navarro, 1988). Under static osmotic pressure, the main osmotic effectors in shellfish hemolymph are balanced by the organic and inorganic ions in the external water environment, and cells will not expand or shrink and the organism can carry out normal life processes (Pasantes-Morales and Schousboe, 1997; Wilder et al., 1998). Although marine shellfish do not have a specific osmotic regulation organ, the gill tissue performs most of this function. Gill tissue and the hepatopancreas of the scallop Argopecten irradians were substantially damaged under extreme salinity stress. Previous studies demonstrated that increased dietary sodium chloride (salt) intake stimulated endothelial cells to produce TGF-β (Ying and Sanders, 1998, 1999, 2002, 2003; Ying et al., 2008, 2012), which led to increased levels of phosphorylated Smad2 (S465/467) (Ying et al., 2013). However, the role of Smads in regulation of salt concentration by the gills in mollusks is poorly understood. Therefore, we investigated the temporal expression of genes involved in BMP2-Smads signaling and immunity in the gills of P. f. martensii after stress treatment with different salinity concentrations.
Both low salinity (16 or/and 20) and high salinity (32 or/and 36) stress significantly up-regulated the mRNA expression of BMP2, Smad4, Smad1/5, Smad6, and MSX, indicating that the gills may control water flow in and out of the organism under salinity stress by increasing the expression level of BMP2-Smads signals. The effect of low salinity on BMP2-Smad signaling occurred mainly within 24 h, whereas the effect of high salinity lasted for more than 24 h. This result suggests that P. f. martensii may be better able to adapt to a low salinity environment than to a high salinity environment, which is consistent with our previous studies of osmoregulation in this species (Pan et al., 2020). The pattern of Smad3 expression was opposite that of Smad6, which was similar to the results for wound healing, and it suggests that Smad3 and Smad6 may have opposing function.
Many studies have reported that salinity stress is closely related to immunity and that salinity stress can cause an immune response. Therefore, we evaluated the expression of important immune genes in P. f. martensii after salinity stress. The patterns of mRNA expression of IL-17, TIMP, CuZn-SOD, and LITAF were similar to those observed for the BMP2-Smads signaling genes, which suggests that BMP2-Smads signaling may be closely related to the immune response of P. f. martensii in addition to participating in osmotic pressure regulation. The duration of up-regulation of these genes during high salinity stress was longer than that during low salinity stress, which also supports the premise that P. f. martensii may more easily to adapt to a low salinity environment.
Previous researchers found that the TGF-β/Smad pathway can regulate IL-17 as part of immunity in vertebrates (Xie et al., 2016; Chen et al., 2018), and several studies reported that CuZn-SOD is involved in the immune response in mollusks (Kim et al., 2007; Ni et al., 2007; Lin et al., 2008; Bao et al., 2009; Li et al., 2010). Additionally, LITAF homologs were identified and characterized from C. gigas, the scallop Chlamys farreri, and P. f. martensii that were exposed to LPS or virus challenge (Yu et al., 2007; Park et al., 2008; Zhang et al., 2009).
The Smad DNA-binding motif was previously found in the promoter regions of MMP and TIMP, which suggests that they may be the direct target genes of Smads (Verrecchia et al., 2001; Qureshi et al., 2008). Kubota et al. (2017) showed that TIMP and MMP were involved in shell wound repair, and Montagnani et al. (2001) reported similar functions were for TIMP in C. gigas. We found that the mRNA expression of MMP in P. f. martensii was up-regulated or down-regulated by high salinity or low salinity stress, respectively, which suggests that MMP may be involved in the immune response to salinity stress via a complex signaling pathway. NF-κB is a classic, evolutionarily conserved, mediator of immune responses in vertebrates (Ghosh et al., 1998), and it also plays an important role in innate immune responses in P. f. martensii (Huang et al., 2012). The down-regulated expression of NF-κB after both high and low salinity stress suggests that it was involved in the immune response to salinity stress.
5 CONCLUSIONPhylogenetic analysis showed that Smad6 of P. f. martensii is located in the Smad6 cluster, which illustrates conservation of the Smads family. The tissue distribution of Smad6 suggests its possible role in immunity, and the expression pattern of Smad6 in different developmental stages indicates that it likely plays a crucial role in development at embryonic stages, but not larval stages. The increased expression of Smad3 and Smad6 mRNAs in mantle tissue after LPS and Poly (I:C) challenge show that they may be involved in innate immunity against bacterial and viral infections. Their expression patterns during wound healing suggest that Smad3 may play a positive role while Smad6 may play a negative role in this process. The temporal expression patterns of genes involved in BMP2-Smads signaling and immunity in the gills after stress treatment with different salinities suggest that the gills control waterflow during salinity stress by increasing the expression level of BMP2-Smads signals and that BMP2-Smads signaling may also be closely related to the immune response of P. f. martensii. Finally, Smad6 and Smad3 may counteract each other during wound healing and salinity stress.
6 DATA AVAILABILITY STATEMENTAll data generated or analyzed during this study are included in this article.
7 AUTHOR CONTRIBUTIONYu SHI planned and designed the research. Maoxian HE supervised the experiments. Yu SHI performed most of the experiments, analyzed data, and wrote the paper. Meng XU performed the challenge assay, Xiaolan PAN and Huiru LIU performed the wound healing experiment; and Hanzhi XU helped perform the salinity stress assay. All authors reviewed, edited, and revised the manuscript.
Adema C M, Hanington P C, Lun C M, Rosenberg G H, Aragon A D, Stout B A, Lennard Richard M L, Gross P S, Loker E S. 2010. Differential transcriptomic responses of Biomphalaria glabrata (Gastropoda, Mollusca) to bacteria and metazoan parasites, Schistosoma mansoni and Echinostoma paraensei (Digenea, Platyhelminthes). Molecular Immunology, 47(4): 849-860.
DOI:10.1016/j.molimm.2009.10.019 |
Bai S T, Cao X. 2002. A nuclear antagonistic mechanism of inhibitory Smads in transforming growth factor-β signaling. Journal of Biological Chemistry, 277(6): 4176-4182.
DOI:10.1074/jbc.M105105200 |
Bai S T, Shi X M, Yang X L, Cao X. 2000. Smad6 as a transcriptional corepressor. Journal of Biological Chemistry, 275(12): 8267-8270.
DOI:10.1074/jbc.275.12.8267 |
Bao Y B, Li L, Xu F, Zhang G F. 2009. Intracellular copper/zinc superoxide dismutase from bay scallop Argopecten irradians: its gene structure, mRNA expression and recombinant protein. Fish & Shellfish Immunology, 27(2): 210-220.
DOI:10.1016/j.fsi.2009.04.005 |
Chen S, Han Y T, Chen H, Wu J, Zhang M. 2018. Bcl11b regulates IL-17 through the TGF-β/Smad pathway in HDM-induced asthma. Allergy, Asthma & Immunology Research, 10(5): 543-545.
DOI:10.4168/aair.2018.10.5.543 |
Choi K C, Lee Y S, Lim S, Choi H K, Lee C H, Lee E K, Hong S, Kim I H, Kim S J, Park S H. 2006. Smad6 negatively regulates interleukin 1-receptor-Toll-like receptor signaling through direct interaction with the adaptor Pellino-1. Nature Immunology, 7(10): 1057-1065.
DOI:10.1038/ni1383 |
De Zoysa M, Lee J. 2009. Suppressor of cytokine signaling 2 (SOCS-2) homologue in disk abalone: cloning, sequence characterization and expression analysis. Fish & Shellfish Immunology, 26(3): 500-508.
DOI:10.1016/j.fsi.2009.02.006 |
Ghosh S, May M J, Kopp E B. 1998. NF-κB and Rel proteins: evolutionarily conserved mediators of immune responses. Annual Review of Immunology, 16: 225-260.
DOI:10.1146/annurev.immunol.16.1.225 |
Goto K, Kamiya Y, Imamura T, Miyazono K, Miyazawa K. 2007. Selective inhibitory effects of Smad6 on bone morphogenetic protein type I receptors. Journal of Biological Chemistry, 282(28): 20603-20611.
DOI:10.1074/jbc.M702100200 |
Hanyu A, Ishidou Y, Ebisawa T, Shimanuki T, Imamura T, Miyazono K. 2001. The N domain of Smad7 is essential for specific inhibition of transforming growth factor-β signaling. Journal of Cell Biology, 155(6): 1017-1028.
DOI:10.1083/jcb.200106023 |
Hata A, Lagna G, Massagué J, Hemmati-Brivanlou A. 1998. Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor. Genes & Development, 12(2): 186-197.
DOI:10.1101/gad.12.2.186 |
Herpin A, Lelong C, Becker T, Rosa F, Favrel P, Cunningham C. 2005. Structural and functional evidence for a singular repertoire of BMP receptor signal transducing proteins in the lophotrochozoan Crassostrea gigas suggests a shared ancestral BMP/activin pathway. The FEBS Journal, 272(13): 3424-3440.
DOI:10.1111/j.1742-4658.2005.04761.x |
Hu B Q, Yi P P, Li Z F, Zhang M, Wen C G, Jian S Q, Yang G. 2017. Molecular characterization of two distinct Smads gene and their roles in the response to bacteria change and wound healing from Hyriopsis cumingii. Fish & Shellfish Immunology, 67: 129-140.
DOI:10.1016/j.fsi.2017.05.052 |
Huang X D, Liu W G, Guan Y Y, Shi Y, Wang Q, Zhao M, Wu S Z, He M X. 2012. Molecular cloning and characterization of class I NF-κB transcription factor from pearl oyster (Pinctada fucata). Fish & Shellfish Immunology, 33(3): 659-666.
DOI:10.1016/j.fsi.2012.06.029 |
Iijima M, Takeuchi T, Sarashina I, Endo K. 2008. Expression patterns of engrailed and dpp in the gastropod Lymnaea stagnalis. Development Genes and Evolution, 218(5): 237-251.
DOI:10.1007/s00427-008-0217-0 |
Ishida W, Hamamoto T, Kusanagi K, Yagi K, Kawabata M, Takehara K, Sampath T K, Kato M, Miyazono K. 2000. Smad6 is a Smad1/5-induced smad inhibitor characterization of bone morphogenetic protein-responsive element in the mouse Smad6 promoter. Journal of Biological Chemistry, 275(9): 6075-6079.
DOI:10.1074/jbc.275.9.6075 |
Itoh F, Asao H, Sugamura K, Heldin C H, ten Dijke P, Itoh S. 2001. Promoting bone morphogenetic protein signaling through negative regulation of inhibitory Smads. The EMBO Journal, 20(15): 4132-4142.
DOI:10.1093/emboj/20.15.4132 |
Kim K Y, Lee S Y, Cho Y S, Bang I C, Kim K H, Kim D S, Nam Y K. 2007. Molecular characterization and mRNA expression during metal exposure and thermal stress of copper/zinc- and manganese-superoxide dismutases in disk abalone, Haliotis discus discus. Fish & Shellfish Immunology, 23(5): 1043-1059.
DOI:10.1016/j.fsi.2007.04.010 |
Kitamura S I, Jung S J, Suzuki S. 2000. Seasonal change of infective state of marine birnavirus in Japanese pearl oyster Pinctada fucata. Archives of Virology, 145(10): 2003-2014.
DOI:10.1007/s007050070036 |
Kubota K, Tsuchihashi Y, Kogure T, Maeyama K, Hattori F, Kinoshita S, Sakuda S, Nagasawa H, Yoshimura E, Suzuki M. 2017. Structural and functional analyses of a TIMP and MMP in the ligament of Pinctada fucata. Journal of Structural Biology, 199(3): 216-224.
DOI:10.1016/j.jsb.2017.07.010 |
Le Quéré H, Herpin A, Huvet A, Lelong C, Favrel P. 2009. Structural and functional characterizations of an activin type II receptor orthologue from the pacific oyster Crassostrea gigas. Gene, 436(1-2): 101-107.
DOI:10.1016/j.gene.2009.01.010 |
Lee Y S, Park J S, Kim J H, Jung S M, Lee J Y, Kim S J, Park S H. 2011. Smad6-specific recruitment of Smurf E3 ligases mediates TGF-β1-induced degradation of MyD88 in TLR4 signalling. Nature Communications, 2: 460.
DOI:10.1038/ncomms1469 |
Lelong C, Badariotti F, Le Quéré H, Rodet F, Dubos M P, Favrel P. 2007. Cg-TGF-β, a TGF-β/activin homologue in the Pacific Oyster Crassostrea gigas, is involved in immunity against Gram-negative microbial infection. Developmental & Comparative Immunology, 31(1): 30-38.
DOI:10.1016/j.dci.2006.05.005 |
Li C H, Sun H L, Chen A Q, Ning X X, Wu H F, Qin S, Xue Q Z, Zhao J M. 2010. Identification and characterization of an intracellular Cu, Zn-superoxide dismutase (icCu/Zn-SOD) gene from clam Venerupis philippinarum. Fish & Shellfish Immunology, 28(3): 499-503.
DOI:10.1016/j.fsi.2009.11.021 |
Li Z F, Zhu M X, Hu B Q, Liu W X, Wu J L, Wen C G, Jian S Q, Yang G. 2020. Effects of suppressing Smads expression on wound healing in Hyriopsis cumingii. Fish & Shellfish Immunology, 97: 455-464.
DOI:10.1016/j.fsi.2019.12.062 |
Lieber M J, Luckhart S. 2004. Transforming growth factor-βs and related gene products in mosquito vectors of human malaria parasites: signaling architecture for immunological crosstalk. Molecular Immunology, 41(10): 965-977.
DOI:10.1016/j.molimm.2004.06.001 |
Lin Y C, Vaseeharan B, Chen J C. 2008. Identification of the extracellular copper-zinc superoxide dismutase (ecCuZnSOD) gene of the mud crab Scylla serrata and its expression following β-glucan and peptidoglycan injections. Molecular Immunology, 45(5): 1346-1355.
DOI:10.1016/j.molimm.2007.09.005 |
Liu G, Huan P, Liu B Z. 2014. Cloning and expression patterns of two Smad genes during embryonic development and shell formation of the Pacific oyster Crassostrea gigas. Chinese Journal of Oceanology and Limnology, 32(6): 1224-1231.
DOI:10.1007/s00343-014-3360-7 |
Miyashita T, Hanashita T, Toriyama M, Takagi R, Akashika T, Higashikubo N. 2008. Gene cloning and biochemical characterization of the BMP-2 of Pinctada fucata. Bioscience, Biotechnology, and Biochemistry, 72(1): 37-47.
DOI:10.1271/bbb.70302 |
Miyazaki T, Goto K, Kobayashi T, Kageyama T, Miyata M. 1999. Mass mortalities associated with a virus disease in Japanese pearl oysters Pinctada fucata martensii. Diseases of Aquatic Organisms, 37(1): 1-12.
DOI:10.3354/dao037001 |
Mokoena D, Sundar S, Kumar D, Houreld NN, Abrahamse H. 2018. Role of photobiomodulation on the activation of the Smad pathway via TGF-beta in wound healing. J. Photoch. Photobio. B, 189: 138-144.
DOI:10.1016/j.jphotobiol.2018.10.011 |
Montagnani C, Le Roux F, Berthe F, Escoubas J M. 2001. Cg-TIMP, an inducible tissue inhibitor of metalloproteinase from the Pacific oyster Crassostrea gigas with a potential role in wound healing and defense mechanisms. FEBS Letters, 500(1-2): 64-70.
DOI:10.1016/S0014-5793(01)02559-5 |
Navarro J M. 1988. The effects of salinity on the physiological ecology of Choromytilus chorus (Molina, 1782) (Bivalvia, Mytilidae). Journal of Experimental Marine Biology and Ecology, 122(1): 19-33.
DOI:10.1016/0022-0981(88)90209-2 |
Nederbragt A J, van Loon A E, Dictus W J A G. 2002. Expression of Patella vulgata orthologs of engrailed and dpp-BMP2/4 in adjacent domains during molluscan shell development suggests a conserved compartment boundary mechanism. Developmental Biology, 246(2): 341-355.
DOI:10.1006/dbio.2002.0653 |
Ni D J, Song L S, Gao Q, Wu L T, Yu Y D, Zhao J M, Qiu L M, Zhang H, Shi F F. 2007. The cDNA cloning and mRNA expression of cytoplasmic Cu, Zn superoxide dismutase (SOD) gene in scallop Chlamys farreri. Fish & Shellfish Immunology, 23(5): 1032-1042.
DOI:10.1016/j.fsi.2007.04.008 |
Nicholas H R, Hodgkin J. 2004. Responses to infection and possible recognition strategies in the innate immune system of Caenorhabditis elegans. Molecular Immunology, 41(5): 479-493.
DOI:10.1016/j.molimm.2004.03.037 |
Pan X L, Liu H R, Xu M, Xu H Z, Zhang H, He M X. 2020. Cloning and expression analysis of aquaporin gene AQP4 cDNA from Pinctada fucata martensii. Journal of Tropical Oceanography, 39(3): 66-75.
(in Chinese with English abstract) DOI:10.11978/2019074 |
Park E M, Kim Y O, Nam B H, Kong H J, Kim W J, Lee S J, Kong I S, Choi T J. 2008. Cloning, characterization and expression analysis of the gene for a putative lipopolysaccharide-induced TNF-α factor of the Pacific oyster, Crassostrea gigas. Fish & Shellfish Immunology, 24(1): 11-17.
DOI:10.1016/j.fsi.2007.07.003 |
Pasantes-Morales H, Schousboe A. 1997. Role of taurine in osmoregulation in brain cells: mechanisms and functional implications. Amino Acids, 12(3): 281-292.
DOI:10.1007/BF01373008 |
Potasman I, Paz A, Odeh M. 2002. Infectious outbreaks associated with bivalve shellfish consumption: a worldwide perspective. Clinical Infectious Diseases, 35(8): 921-928.
DOI:10.1086/342330 |
Qureshi H Y, Ricci G, Zafarullah M. 2008. Smad signaling pathway is a pivotal component of tissue inhibitor of metalloproteinases-3 regulation by transforming growth factor beta in human chondrocytes. Biochimica et Biophysica Acta (BBA)-Molecular Cell Research, 1783(9): 1605-1612.
DOI:10.1016/j.bbamcr.2008.04.005 |
Raftery L A, Sutherland D J. 1999. TGF-β family signal transduction in Drosophila development: from Mad to Smads. Developmental Biology, 210(2): 251-268.
DOI:10.1006/dbio.1999.9282 |
Reinhardt B, Broun M, Blitz I L, Bode H R. 1996. HyBMP5-8b, a BMP5-8 orthologue, acts during axial patterning and tentacle formation in hydra. Developmental Biology, 267(1): 790-794.
DOI:10.1016/j.ydbio.2003.10.031 |
Savage C, Das P, Finelli A L, Townsend S R, Sun C Y, Baird S E, Padgett R W. 1996. Caenorhabditis elegans genes sma-2, sma-3, and sma-4 define a conserved family of transforming growth factor beta pathway components. Proceedings of the National Academy of Sciences of the United States of America, 93(2): 790-794.
DOI:10.1073/pnas.93.2.790 |
Shi Y, Liu X C, Zhang H F, Zhang Y, Lu D Q, Lin H R. 2012. Molecular identification of an androgen receptor and its changes in mRNA levels during 17α-methyltestosterone-induced sex reversal in the orange-spotted grouper Epinephelus coioides. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 163(1): 43-50.
DOI:10.1016/j.cbpb.2012.04.011 |
Shi Y, Pan X L, Xu M, Liu H R, Xu H Z, He M X. 2021. The role of Smad1/5 in mantle immunity of the pearl oyster Pinctada fucata martensii. Fish & Shellfish Immunology, 113: 208-215.
DOI:10.1016/j.fsi.2021.04.001 |
Shi Y, Zhao M, He M X. 2020. PfSMAD1/5 Can interact with PfSMAD4 to inhibit PfMSX to regulate shell biomineralization in Pinctada fucata martensii. Marine Biotechnology, 22(2): 246-262.
DOI:10.1007/s10126-020-09948-5 |
Shimizu K, Sarashina I, Kagi H, Endo K. 2011. Possible functions of Dpp in gastropod shell formation and shell coiling. Development Genes and Evolution, 221(2): 59.
DOI:10.1007/s00427-011-0358-4 |
Verrecchia F, Chu M L, Mauviel A. 2001. Identification of novel TGF-β/Smad gene targets in dermal fibroblasts using a combined cDNA microarray/promoter transactivation approach. Journal of Biological Chemistry, 276(20): 17058-17062.
DOI:10.1074/jbc.M100754200 |
von Bubnoff A, Cho K W Y. 2001. Intracellular BMP signaling regulation in vertebrates: pathway or network?. Developmental Biology, 239(1): 1-14.
DOI:10.1006/dbio.2001.0388 |
Wilder M N, Ikuta K, Atmomarsono M, Hatta T, Komuro K. 1998. Changes in osmotic and ionic concentrations in the hemolymph of Macrobrachium rosenbergii exposed to varying salinities and correlation to ionic and crystalline composition of the cuticle. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology, 119(4): 941-950.
DOI:10.1016/S1095-6433(98)00008-7 |
Xie Y H, Li X P, Xu Z X, Qian P, Li X L, Wang Y Q. 2016. Effect of compound Maqin decoction on TGF-β1/Smad proteins and IL-10 and IL-17 content in lung tissue of asthmatic rats. Genetics and Molecular Research, 15(3): gmr7539.
DOI:10.4238/gmr.15037539 |
Xu F, Liu C, Zhou D, Zhang L. 2016. TGF-beta/SMAD Pathway and Its Regulation in Hepatic Fibrosis. J. Histochem. Cytochem., 64: 157-67.
DOI:10.1369/0022155415627681 |
Ying W Z, Aaron K J, Sanders P W. 2013. Transforming growth factor-β regulates endothelial function during high salt intake in rats. Hypertension, 62(5): 951-956.
DOI:10.1161/hypertensionaha.113.01835 |
Ying W Z, Aaron K, Sanders P W. 2008. Mechanism of dietary salt-mediated increase in intravascular production of TGF-β1. American Journal of Physiology-Renal Physiology, 295(2): F406-F414.
DOI:10.1152/ajprenal.90294.2008 |
Ying W Z, Sanders P W. 1998. Dietary salt enhances glomerular endothelial nitric oxide synthase through TGF-β1. American Journal of Physiology-Renal Physiology, 275(1): F18-F24.
DOI:10.1152/ajprenal.1998.275.1.F18 |
Ying W Z, Sanders P W. 1999. Dietary salt increases endothelial nitric oxide synthase and TGF-β1 in rat aortic endothelium. American Journal of Physiology-Renal Physiology, 277(4): H1293-H1298.
DOI:10.1152/ajpheart.1999.277.4.H1293 |
Ying W Z, Sanders P W. 2002. Increased dietary salt activates rat aortic endothelium. Hypertension, 39(2): 239-244.
DOI:10.1161/hy0202.104142 |
Ying W Z, Sanders P W. 2003. The interrelationship between TGF-β1 and nitric oxide is altered in salt-sensitive hypertension. American Journal of Physiology-Renal Physiology, 285(5): F902-F908.
DOI:10.1152/ajprenal.00177.2003 |
Ying W Z., Aaron K J, Sanders P W. 2012. Effect of aging and dietary salt and potassium intake on endothelial PTEN (Phosphatase and tensin homolog on chromosome 10) function. PLoS One, 7(11): e48715.
DOI:10.1371/journal.pone.0048715 |
Yu Y D, Qiu L M, Song L S, Zhao J M, Ni D J, Zhang Y, Xu W. 2007. Molecular cloning and characterization of a putative lipopolysaccharide-induced TNF-α factor (LITAF) gene homologue from Zhikong scallop Chlamys farreri. Fish & Shellfish Immunology, 23(2): 419-429.
DOI:10.1016/j.fsi.2006.12.004 |
Zhang D C, Jiang J J, Jiang S G, Ma J J, Su T F, Qiu L H, Zhu C Y, Xu X P. 2009. Molecular characterization and expression analysis of a putative LPS-induced TNF-α factor (LITAF) from pearl oyster Pinctada fucata. Fish & Shellfish Immunology, 27(3): 391-396.
DOI:10.1016/j.fsi.2009.04.006 |
Zhang T, Wu J, Ungvijanpunya N, Jackson-Weaver O, Gou Y, Feng J, Ho T V, Shen Y, Liu J, Richard S, Jin J, Hajishengallis G, Chai Y, Xu J. 2018. Smad6 methylation represses NFκB Activation and periodontal inflammation. Journal of Dental Research, 97(7): 810-819.
DOI:10.1177/0022034518755688 |
Zhang Y, Feng X H, Wu R Y, Derynck R. 1996. Receptor-associated Mad homologues synergize as effectors of the TGF-β response. Nature, 383(6596): 168-172.
DOI:10.1038/383168a0 |
Zhao M, Shi Y, He M X, Huang X D, Wang Q. 2016. PfSMAD4 plays a role in biomineralization and can transduce bone morphogenetic protein-2 signals in the pearl oyster Pinctada fucata. BMC Developmental Biology, 16: 9.
DOI:10.1186/s12861-016-0110-4 |
Zoccola D, Moya A, Béranger G E, Tambutté E, Allemand D, Carle G F, Tambutté S. 2009. Specific expression of BMP2/4 ortholog in biomineralizing tissues of corals and action on mouse BMP receptor. Marine Biotechnology, 11(2): 260-269.
DOI:10.1007/s10126-008-9141-6 |