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创伤愈合的修订:体外和计算模型揭示的新型再上皮化机制。

Wound healing revised: a novel reepithelialization mechanism revealed by in vitro and in silico models.

机构信息

Hamamatsu Tissue Imaging and Analysis Center, BIOQUANT, and 2 Department of Medical Oncology, National Center for Tumor Diseases, University of Heidelberg, 69117 Heidelberg, Germany.

出版信息

J Cell Biol. 2013 Nov 25;203(4):691-709. doi: 10.1083/jcb.201212020.

Abstract

Wound healing is a complex process in which a tissue's individual cells have to be orchestrated in an efficient and robust way. We integrated multiplex protein analysis, immunohistochemical analysis, and whole-slide imaging into a novel medium-throughput platform for quantitatively capturing proliferation, differentiation, and migration in large numbers of organotypic skin cultures comprising epidermis and dermis. Using fluorescent time-lag staining, we were able to infer source and final destination of keratinocytes in the healing epidermis. This resulted in a novel extending shield reepithelialization mechanism, which we confirmed by computational multicellular modeling and perturbation of tongue extension. This work provides a consistent experimental and theoretical model for epidermal wound closure in 3D, negating the previously proposed concepts of epidermal tongue extension and highlighting the so far underestimated role of the surrounding tissue. Based on our findings, epidermal wound closure is a process in which cell behavior is orchestrated by a higher level of tissue control that 2D monolayer assays are not able to capture.

摘要

伤口愈合是一个复杂的过程,其中组织的单个细胞必须以高效和稳健的方式进行协调。我们将多重蛋白质分析、免疫组织化学分析和全玻片成像集成到一个新的高通量平台中,用于定量捕获大量包含表皮和真皮的器官型皮肤培养物中的增殖、分化和迁移。使用荧光时滞染色,我们能够推断出愈合表皮中角质形成细胞的来源和最终去向。这导致了一种新的扩展屏蔽再上皮化机制,我们通过计算多细胞建模和对舌延伸的干扰来证实了这一机制。这项工作为 3D 中的表皮伤口闭合提供了一个一致的实验和理论模型,否定了先前提出的表皮舌延伸概念,并强调了迄今为止被低估的周围组织的作用。基于我们的发现,表皮伤口闭合是一个细胞行为由更高层次的组织控制协调的过程,而 2D 单层测定无法捕捉到这一过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/842c/3840932/5134b239b148/JCB_201212020_Fig1.jpg

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