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损伤触发筋膜成纤维细胞集体细胞迁移,通过 N-钙黏蛋白驱动瘢痕形成。

Injury triggers fascia fibroblast collective cell migration to drive scar formation through N-cadherin.

机构信息

Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine, Munich, Germany.

Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Systems Medicine of Chronic Lung Disease, Munich, Germany.

出版信息

Nat Commun. 2020 Nov 6;11(1):5653. doi: 10.1038/s41467-020-19425-1.

Abstract

Scars are more severe when the subcutaneous fascia beneath the dermis is injured upon surgical or traumatic wounding. Here, we present a detailed analysis of fascia cell mobilisation by using deep tissue intravital live imaging of acute surgical wounds, fibroblast lineage-specific transgenic mice, and skin-fascia explants (scar-like tissue in a dish - SCAD). We observe that injury triggers a swarming-like collective cell migration of fascia fibroblasts that progressively contracts the skin and form scars. Swarming is exclusive to fascia fibroblasts, and requires the upregulation of N-cadherin. Both swarming and N-cadherin expression are absent from fibroblasts in the upper skin layers and the oral mucosa, tissues that repair wounds with minimal scar. Impeding N-cadherin binding inhibits swarming and skin contraction, and leads to reduced scarring in SCADs and in animals. Fibroblast swarming and N-cadherin thus provide therapeutic avenues to curtail fascia mobilisation and pathological fibrotic responses across a range of medical settings.

摘要

当真皮下的皮下筋膜在手术或创伤性损伤时受伤时,疤痕会更加严重。在这里,我们通过对急性手术伤口的深层组织活体成像、成纤维细胞谱系特异性转基因小鼠和皮肤筋膜外植体(盘中的瘢痕样组织-SCAD),详细分析了筋膜细胞的动员。我们观察到损伤会引发筋膜成纤维细胞的群集样集体迁移,这些细胞逐渐收缩皮肤并形成疤痕。群集现象是筋膜成纤维细胞所特有的,需要 N-钙黏蛋白的上调。在上层皮肤和口腔黏膜的成纤维细胞中,既不存在群集现象,也不存在 N-钙黏蛋白的表达,这些组织在修复伤口时几乎没有疤痕。阻碍 N-钙黏蛋白结合会抑制群集和皮肤收缩,从而减少 SCAD 中的疤痕形成和动物中的疤痕形成。因此,成纤维细胞的群集和 N-钙黏蛋白为抑制筋膜动员和各种医疗环境中的病理性纤维化反应提供了治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d061/7648088/9a3028d0229b/41467_2020_19425_Fig1_HTML.jpg

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