Kwack Kyu Hwan, Lee Hyeon-Woo
Institute of Oral Biology, School of Dentistry, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Mediators Inflamm. 2017;2017:7682083. doi: 10.1155/2017/7682083. Epub 2017 Jan 17.
We have examined the effect of progranulin (PGRN) on human T cell proliferation and its underlying mechanism. We show that PGRN inhibits the PHA-induced multiplication of T lymphocytes. It increases the number of iTregs when T lymphocytes are activated by PHA but does not do so in the absence of PHA. PGRN-mediated inhibition of T lymphocyte proliferation, as well as the induction of iTregs, was completely reversed by a TGF- inhibitor or a Treg inhibitor. PGRN induced TGF- secretion in the presence of PHA whereas it did not in the absence of PHA. Our findings indicate that PGRN suppresses T lymphocyte proliferation by enhancing the formation of iTregs from activated T lymphocytes in response to TGF-.
我们研究了颗粒蛋白前体(PGRN)对人T细胞增殖的影响及其潜在机制。我们发现PGRN抑制PHA诱导的T淋巴细胞增殖。当T淋巴细胞被PHA激活时,PGRN可增加诱导性调节性T细胞(iTregs)的数量,但在无PHA的情况下则不会。TGF-β抑制剂或调节性T细胞抑制剂可完全逆转PGRN介导的T淋巴细胞增殖抑制以及iTregs的诱导。在有PHA存在的情况下,PGRN可诱导TGF-β分泌,而在无PHA时则不会。我们的研究结果表明,PGRN通过增强活化T淋巴细胞响应TGF-β形成iTregs来抑制T淋巴细胞增殖。