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SARA 可抑制硬皮病小鼠模型成纤维细胞前体细胞向肌成纤维细胞的转分化。

SARA suppresses myofibroblast precursor transdifferentiation in fibrogenesis in a mouse model of scleroderma.

机构信息

Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.

Pediatric Nephrology, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.

出版信息

JCI Insight. 2022 Nov 8;7(21):e160977. doi: 10.1172/jci.insight.160977.

Abstract

We previously reported that Smad anchor for receptor activation (SARA) plays a critical role in maintaining epithelial cell phenotype. Here, we show that SARA suppressed myofibroblast precursor transdifferentiation in a mouse model of scleroderma. Mice overexpressing SARA specifically in PDGFR-β+ pericytes and pan-leukocytes (SARATg) developed significantly less skin fibrosis in response to bleomycin injection compared with wild-type littermates (SARAWT). Single-cell RNA-Seq analysis of skin PDGFR-β+ cells implicated pericyte subsets assuming myofibroblast characteristics under fibrotic stimuli, and SARA overexpression blocked the transition. In addition, a cluster that expresses molecules associated with Th2 cells and macrophage activation was enriched in SARAWT mice, but not in SARATg mice, after bleomycin treatment. Th2-specific Il-31 expression was increased in skin of the bleomycin-treated SARAWT mice and patients with scleroderma (or systemic sclerosis, SSc). Receptor-ligand analyses indicated that lymphocytes mediated pericyte transdifferentiation in SARAWT mice, while with SARA overexpression the myofibroblast activity of pericytes was suppressed. Together, these data suggest a potentially novel crosstalk between myofibroblast precursors and immune cells in the pathogenesis of SSc, in which SARA plays a critical role.

摘要

我们之前报道称,Smad 锚蛋白受体激活物(SARA)在维持上皮细胞表型方面起着关键作用。在这里,我们表明 SARA 抑制了硬皮病小鼠模型中的成肌纤维细胞前体转分化。与野生型同窝仔鼠(SARAWT)相比,特异性在 PDGFR-β+周细胞和全白细胞中过表达 SARA 的小鼠(SARATg)在博来霉素注射后皮肤纤维化明显减少。皮肤 PDGFR-β+细胞的单细胞 RNA-Seq 分析表明,在纤维化刺激下,周细胞亚群假定具有成肌纤维细胞特征,而 SARA 过表达则阻断了这种转化。此外,在博来霉素处理后,SARAWT 小鼠中富含表达与 Th2 细胞和巨噬细胞激活相关分子的簇,但 SARATg 小鼠中则没有。在博来霉素处理的 SARAWT 小鼠和硬皮病(或系统性硬化症,SSc)患者的皮肤中,Th2 特异性 Il-31 表达增加。受体-配体分析表明,淋巴细胞介导了 SARAWT 小鼠中周细胞的转分化,而 SARA 过表达则抑制了周细胞的成肌纤维细胞活性。总之,这些数据表明,在 SSc 的发病机制中,成肌纤维细胞前体和免疫细胞之间可能存在一种新的串扰,而 SARA 在其中起着关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e622/9675568/112c58c4c378/jciinsight-7-160977-g131.jpg

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