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骨膜/软骨膜细胞内张力调节长骨生长。

Intracellular tension in periosteum/perichondrium cells regulates long bone growth.

机构信息

Department of Biomedical Engineering, Eindhoven University of Technology, PO Box 513, WH 4.115, 5600 MB Eindhoven, The Netherlands.

出版信息

J Orthop Res. 2011 Jan;29(1):84-91. doi: 10.1002/jor.21224.

Abstract

Perichondrium/periosteum is involved in regulating long bone growth. Long bones grow faster after removal or circumferential division of periosteum. This can be countered by culturing them in conditioned medium from perichondrium/periosteum cells. Because both complete removal and circumferential division are effective, we hypothesized that perichondrium/periosteum cells require an intact environment to release the appropriate soluble factors. More specifically, we propose that this release depends on their ability to generate intracellular tension. This hypothesis was explored by modulating the ability of perichondrium/periosteum cells to generate intracellular tension and monitoring the effect thereof on long bone growth. Perichondrium/periosteum cells were cultured on substrates with different stiffness. The medium produced by these cultures was added to embryonic chick tibiotarsi from which perichondrium/periosteum was either stripped or left intact. After 3 culture days, long bone growth was proportionally related to the stiffness of the substrate on which perichondrium/periosteum cells were grown while they produced conditioned medium. A second set of experiments demonstrated that the effect occurred through expression of a growth-inhibiting factor, rather than through the reduction of a stimulatory factor. Finally, evidence for the importance of intracellular tension was obtained by showing that the inhibitory effect was abolished when perichondrium/periosteum cells were treated with cytochalasin D, which disrupts the actin microfilaments. Thus, we concluded that modulation of long bone growth occurs through release of soluble inhibitors by perichondrium/periosteum cells, and that the ability of cells to develop intracellular tension through their actin microfilaments is at the base of this mechano-regulated control pathway.

摘要

软骨膜/骨膜参与调节长骨生长。去除或环绕骨膜分割后,长骨生长加快。通过在软骨膜/骨膜细胞的条件培养基中培养可以对抗这种情况。因为完全去除和环绕分割都有效,所以我们假设软骨膜/骨膜细胞需要完整的环境才能释放适当的可溶性因子。更具体地说,我们提出这种释放取决于它们产生细胞内张力的能力。通过调节软骨膜/骨膜细胞产生细胞内张力的能力并监测其对长骨生长的影响来探索这一假说。将软骨膜/骨膜细胞培养在具有不同硬度的基质上。从软骨膜/骨膜完整或被剥离的胚胎小鸡胫骨中添加这些培养物产生的培养基。培养 3 天后,长骨生长与软骨膜/骨膜细胞在产生条件培养基时生长的基质的硬度成比例相关。第二组实验表明,这种效应是通过表达生长抑制因子而不是通过减少刺激因子而发生的。最后,通过显示当软骨膜/骨膜细胞用细胞松弛素 D 处理时,这种抑制作用被消除,而细胞松弛素 D 破坏了肌动蛋白微丝,从而获得了细胞内张力重要性的证据。因此,我们得出结论,通过软骨膜/骨膜细胞释放可溶性抑制剂来调节长骨生长,并且细胞通过其肌动蛋白微丝产生细胞内张力的能力是这种机械调节控制途径的基础。

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