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细胞非自主的局部和全身反应使细胞阻滞能够在发育中的小鼠中实现长骨追赶性生长。

Cell-nonautonomous local and systemic responses to cell arrest enable long-bone catch-up growth in developing mice.

机构信息

Developmental Biology Program, Sloan Kettering Institute, New York, New York, United States of America.

Allen Institute for Brain Science, Seattle, Washington, United States of America.

出版信息

PLoS Biol. 2018 Jun 26;16(6):e2005086. doi: 10.1371/journal.pbio.2005086. eCollection 2018 Jun.

Abstract

Catch-up growth after insults to growing organs is paramount to achieving robust body proportions. In fly larvae, injury to individual tissues is followed by local and systemic compensatory mechanisms that allow the damaged tissue to regain normal proportions with other tissues. In vertebrates, local catch-up growth has been described after transient reduction of bone growth, but the underlying cellular responses are controversial. We developed an approach to study catch-up growth in foetal mice in which mosaic expression of the cell cycle suppressor p21 is induced in the cartilage cells (chondrocytes) that drive long-bone elongation. By specifically targeting p21 expression to left hindlimb chondrocytes, the right limb serves as an internal control. Unexpectedly, left-right limb symmetry remained normal, revealing deployment of compensatory mechanisms. Above a certain threshold of insult, an orchestrated response was triggered involving local enhancement of bone growth and systemic growth reduction that ensured that body proportions were maintained. The local response entailed hyperproliferation of spared left limb chondrocytes that was associated with reduced chondrocyte density. The systemic effect involved impaired placental function and IGF signalling, revealing bone-placenta communication. Therefore, vertebrates, like invertebrates, can mount coordinated local and systemic responses to developmental insults that ensure that normal body proportions are maintained.

摘要

追赶生长是受损器官恢复正常生长的关键,对于维持良好的体型比例非常重要。在蝇类幼虫中,单个组织损伤后会引发局部和全身的补偿机制,使受损组织能够与其他组织恢复正常比例。在脊椎动物中,人们已经描述了短暂性骨生长减少后的局部追赶生长,但潜在的细胞反应仍存在争议。我们开发了一种在胎儿小鼠中研究追赶生长的方法,即在驱动长骨伸长的软骨细胞(软骨细胞)中诱导细胞周期抑制剂 p21 的镶嵌表达。通过将 p21 表达特异性靶向左后肢软骨细胞,可以将右肢作为内部对照。出乎意料的是,左右肢对称性仍保持正常,表明补偿机制已经启动。在受到一定程度的损伤后,会引发协调的反应,包括局部增强骨生长和全身生长减少,以确保维持体型比例。局部反应涉及到受保护的左肢软骨细胞的过度增殖,同时伴随着软骨细胞密度的降低。全身效应涉及到胎盘功能和 IGF 信号的受损,揭示了骨-胎盘的通讯。因此,脊椎动物和无脊椎动物一样,可以对发育损伤做出协调的局部和全身反应,以确保维持正常的体型比例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfd1/6019387/3678463ff273/pbio.2005086.g001.jpg

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