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Roles of B7 homologue 3 protein (B7-H3) in T cell responses of large yellow croaker (Larimichthys crocea)
Qiuhua Li1, Yuhong Chen2, Meiyan Wang3
1State Key Laboratory of Mariculture Breeding, Key Laboratory of Marine Biotechnology of Fujian Province, College of Marine Sciences, Fujian Agriculture and Forestry University, Fuzhou, 350002, China; Guangdong Provincial Key Laboratory of Marine Biology, Shantou University, Shantou, 515063, China.
Abstract:
The B7 family provides critical co-stimulatory signals for T cell activation through receptor interactions, thereby modulating T cell proliferation and function. However, the roles and downstream signaling pathways of these molecules in teleosts remain largely unexplored. In the present study, we identified a B7-H3 homologue (LcB7-H3) in large yellow croaker (Larimichthys crocea), a commercially significant marine teleost species. The deduced LcB7-H3 protein contains conserved extracellular IgV-like and IgC-like domains, and phylogenetic analysis revealed its clustering with vertebrate B7-H3 homologues. It is constitutively expressed in all examined tissues and immune cells, with particularly high expression levels in mucosal tissues and primary head kidney monocytes/macrophages (PKMs). The recombinant LcB7-H3 protein (rLcB7-H3) significantly enhanced T cell proliferation and upregulated interleukin-2 expression, which is a hallmark of teleost T cell activation. Furthermore, rLcB7-H3 increased phosphorylation levels of MEK1/2 and ERK1/2 in the MAPK/ERK signaling pathway, as well as mTOR and 4E-BP1 in the mTOR signaling pathway. Collectively, these findings demonstrate that LcB7-H3 may promote T cell proliferation and activation via MAPK/ERK and mTOR pathways, suggesting evolutionarily conserved roles among vertebrate B7-H3 homologues.
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