降钙素基因相关肽/巨噬细胞轴信号促进肠道炎症恢复。

The CGRP/macrophage axis signal facilitates inflammation recovery in the intestine.

作者信息

Wu Wei, Feng Baisui, Liu Jie, Li Yan, Liao Yun, Wang Shiqi, Tao Shuang, Hu Suqin, He Weiyi, Shu Qing, Liu Zhanju, Yang Pingchang

机构信息

Department of Gastroenterology, Shanghai Tenth People's Hospital of Tongji University, Shanghai, China.

Department of Gastroenterology, Second Affiliated Hospital, Zhengzhou University, Zhengzhou, China.

出版信息

Clin Immunol. 2022 Dec;245:109154. doi: 10.1016/j.clim.2022.109154. Epub 2022 Oct 13.

Abstract

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.

摘要

肠道免疫炎症恢复的机制仍有待研究。降钙素相关蛋白(CGRP;一种神经肽)具有免疫调节能力。我们观察到,在溃疡性结肠炎(UC)患者的结肠活检组织中发现CGRP水平较低。在活检样本中,CGRP与肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和干扰素-γ(IFN-γ)呈负相关。UC组中转化生长因子-β(TGF-β)的水平低于正常对照组(NC组),且与CGRP水平呈正相关。阻断CGRP会显著延迟结肠炎炎症的恢复。CGRP可诱导肠道中表达TGF-β的CD4 Tim4巨噬细胞。CD4 Tim4巨噬细胞在抑制结肠炎分离T细胞增殖和诱导T细胞凋亡方面表现出免疫调节功能。巨噬细胞中Tgfb1表达的缺失导致结肠炎炎症恢复显著延迟,而通过在小鼠中重建CD-4 Tim4巨噬细胞可挽救这一情况。

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