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局灶性高细胞密度在自组织血管间充质细胞中产生模式梯度。

Focal high cell density generates a gradient of patterns in self-organizing vascular mesenchymal cells.

作者信息

Cheng Henry, Reddy Aneela, Sage Andrew, Lu Jinxiu, Garfinkel Alan, Tintut Yin, Demer Linda L

机构信息

Department of Medicine, University of California, Los Angeles, CA 90095-1679, USA.

出版信息

J Vasc Res. 2012;49(5):441-6. doi: 10.1159/000339568. Epub 2012 Jul 11.

Abstract

In embryogenesis, structural patterns, such as vascular branching, may form via a reaction-diffusion mechanism in which activator and inhibitor morphogens guide cells into periodic aggregates. We previously found that vascular mesenchymal cells (VMCs) spontaneously aggregate into nodular structures and that morphogen pairs regulate the aggregation into patterns of spots and stripes. To test the effect of a focal change in activator morphogen on VMC pattern formation, we created a focal zone of high cell density by plating a second VMC layer within a cloning ring over a confluent monolayer. After 24 h, the ring was removed and pattern formation monitored by phase-contrast microscopy. At days 2-8, the patterns progressed from uniform distributions to swirl, labyrinthine and spot patterns. Within the focal high-density zone (HDZ) and a narrow halo zone, cells aggregated into spot patterns, whilst in the outermost zone of the plate, cells formed a labyrinthine pattern. The area occupied by aggregates was significantly greater in the outermost zone than in the HDZ or halo. The rate of pattern progression within the HDZ increased as a function of its plating density. Thus, focal differences in cell density may drive pattern formation gradients in tissue architecture, such as vascular branching.

摘要

在胚胎发育过程中,诸如血管分支等结构模式可能通过反应扩散机制形成,其中激活剂和抑制剂形态发生素引导细胞形成周期性聚集体。我们之前发现血管间充质细胞(VMCs)会自发聚集成结节状结构,并且形态发生素对会将聚集调节成斑点和条纹模式。为了测试激活剂形态发生素的局部变化对VMC模式形成的影响,我们通过在融合单层上的克隆环内铺展第二层VMC来创建一个高细胞密度的局部区域。24小时后,移除克隆环,并用相差显微镜监测模式形成。在第2 - 8天,模式从均匀分布发展为漩涡、迷宫和斑点模式。在局部高密度区(HDZ)和一个狭窄的晕圈区内,细胞聚集成斑点模式,而在培养皿的最外层区域,细胞形成迷宫模式。聚集体占据的面积在最外层区域显著大于HDZ或晕圈区。HDZ内模式发展的速率随其铺板密度而增加。因此,细胞密度的局部差异可能驱动组织结构中的模式形成梯度,如血管分支。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd52/3478883/2fec6c7640cb/nihms407851f1.jpg

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本文引用的文献

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