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浸润性脂肪细胞不是肌成纤维细胞。

Wound infiltrating adipocytes are not myofibroblasts.

机构信息

Institute of Regenerative Biology and Medicine, Helmholtz Center Munich, Munich, Germany.

Institute of Lung Health and Immunity, Helmholtz Center Munich, Munich, Germany.

出版信息

Nat Commun. 2023 May 25;14(1):3020. doi: 10.1038/s41467-023-38591-6.

Abstract

The origins of wound myofibroblasts and scar tissue remains unclear, but it is assumed to involve conversion of adipocytes into myofibroblasts. Here, we directly explore the potential plasticity of adipocytes and fibroblasts after skin injury. Using genetic lineage tracing and live imaging in explants and in wounded animals, we observe that injury induces a transient migratory state in adipocytes with vastly distinct cell migration patterns and behaviours from fibroblasts. Furthermore, migratory adipocytes, do not contribute to scar formation and remain non-fibrogenic in vitro, in vivo and upon transplantation into wounds in animals. Using single-cell and bulk transcriptomics we confirm that wound adipocytes do not convert into fibrogenic myofibroblasts. In summary, the injury-induced migratory adipocytes remain lineage-restricted and do not converge or reprogram into a fibrosing phenotype. These findings broadly impact basic and translational strategies in the regenerative medicine field, including clinical interventions for wound repair, diabetes, and fibrotic pathologies.

摘要

伤口肌成纤维细胞和瘢痕组织的起源仍不清楚,但据推测涉及脂肪细胞向肌成纤维细胞的转化。在这里,我们直接探索皮肤损伤后脂肪细胞和成纤维细胞的潜在可塑性。使用遗传谱系追踪和在皮片和受伤动物中的活体成像,我们观察到损伤诱导脂肪细胞短暂的迁移状态,其迁移模式和行为与成纤维细胞有很大的不同。此外,迁移的脂肪细胞不参与瘢痕形成,并且在体外、体内以及在动物伤口移植后仍然是非纤维生成的。使用单细胞和批量转录组学,我们证实伤口脂肪细胞不会转化为纤维生成的肌成纤维细胞。总之,损伤诱导的迁移脂肪细胞保持谱系特异性,不会融合或重新编程为纤维表型。这些发现广泛影响再生医学领域的基础和转化策略,包括伤口修复、糖尿病和纤维化病理的临床干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9d6/10213017/af40fcefc6e1/41467_2023_38591_Fig1_HTML.jpg

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