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三维细胞的分隔几何形状和动力学由组织表面张力调节控制。

3D cell segregation geometry and dynamics are governed by tissue surface tension regulation.

机构信息

Department of Biological Physics, ELTE Eötvös University, Budapest, Hungary.

Department of Genetics, ELTE Eötvös University, Budapest, Hungary.

出版信息

Commun Biol. 2023 Aug 4;6(1):817. doi: 10.1038/s42003-023-05181-7.

Abstract

Tissue morphogenesis and patterning during development involve the segregation of cell types. Segregation is driven by differential tissue surface tensions generated by cell types through controlling cell-cell contact formation by regulating adhesion and actomyosin contractility-based cellular cortical tensions. We use vertebrate tissue cell types and zebrafish germ layer progenitors as in vitro models of 3-dimensional heterotypic segregation and developed a quantitative analysis of their dynamics based on 3D time-lapse microscopy. We show that general inhibition of actomyosin contractility by the Rho kinase inhibitor Y27632 delays segregation. Cell type-specific inhibition of non-muscle myosin2 activity by overexpression of myosin assembly inhibitor S100A4 reduces tissue surface tension, manifested in decreased compaction during aggregation and inverted geometry observed during segregation. The same is observed when we express a constitutively active Rho kinase isoform to ubiquitously keep actomyosin contractility high at cell-cell and cell-medium interfaces and thus overriding the interface-specific regulation of cortical tensions. Tissue surface tension regulation can become an effective tool in tissue engineering.

摘要

组织形态发生和发育过程中的模式形成涉及细胞类型的分离。通过调节细胞间的接触形成,控制黏附以及基于肌动球蛋白收缩性的细胞皮层张力,细胞类型通过产生不同的组织表面张力来驱动分离。我们使用脊椎动物组织细胞类型和斑马鱼胚层祖细胞作为三维异质分离的体外模型,并基于 3D 延时显微镜开发了对其动力学的定量分析。我们表明,通过 Rho 激酶抑制剂 Y27632 普遍抑制肌动球蛋白收缩会延迟分离。通过过表达肌球蛋白组装抑制剂 S100A4 特异性抑制非肌肉肌球蛋白 2 活性,会降低组织表面张力,表现为聚集过程中致密性降低以及在分离过程中观察到的几何形状倒置。当我们表达组成型激活的 Rho 激酶同工型以使肌动球蛋白收缩性在细胞-细胞和细胞-培养基界面普遍升高并因此覆盖皮层张力的界面特异性调节时,也会观察到同样的现象。组织表面张力的调节可能成为组织工程中的有效工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb6/10403547/dbc5d4d7a0e3/42003_2023_5181_Fig1_HTML.jpg

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