降钙素基因相关肽
炎症
免疫系统
结肠炎
内分泌学
巨噬细胞
内科学
化学
免疫学
神经肽
医学
生物
受体
生物化学
体外
作者
Wei Wu,Bai‐Sui Feng,Jie Liu,Yan Li,Yun Liao,Shiqi Wang,Shuang Tao,Suqin Hu,Weiyi He,Qing Shu,Zhanju Liu,Ping‐Chang Yang
标识
DOI:10.1016/j.clim.2022.109154
摘要
The mechanism of the recovery of immune inflammation in the intestine remains to be investigated. The calcitonin-related protein (CGRP; neuropeptide) has immune regulatory capacity. We observed that lower levels of CGRP were found in the colon biopsies of UC patients. CGRP were negatively correlated to TNF-α, IL-1β and IFN-γ in biopsy samples. The levels of TGF-β were lower in the UC group than that of the normal control (NC) group, which were positively correlated with the CGRP levels. Blocking CGRP significantly delayed recovery from colitis inflammation. CGRP induced the TGF-β-expressing CD4+ Tim4+ macrophages in the intestine. CD4+ Tim4+ macrophages demonstrated immune regulatory function in suppressing proliferation of isolated T cells of colitis and induced apoptosis of T cells. Ablation of the Tgfb1 expression in macrophages resulted in a significant delay in recovery of inflammation in colitis, which was rescued by reconstitution of the CD4+ Tim4+ macrophages in mice.
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