Caspases and matrix metalloproteases facilitate collective behavior of non-neural ectoderm after hindbrain neuropore closure.

Q2 Biochemistry, Genetics and Molecular Biology BMC Developmental Biology Pub Date : 2018-07-31 DOI:10.1186/s12861-018-0175-3
Naomi Shinotsuka, Yoshifumi Yamaguchi, Kenichi Nakazato, Yudai Matsumoto, Atsushi Mochizuki, Masayuki Miura
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引用次数: 7

Abstract

Background: Mammalian brain is formed through neural tube closure (NTC), wherein both ridges of opposing neural folds are fused in the midline and remodeled in the roof plate of the neural tube and overlying non-neural ectodermal layer. Apoptosis is widely observed from the beginning of NTC at the neural ridges and is crucial for the proper progression of NTC, but its role after the closure remains less clear.

Results: Here, we conducted live-imaging analysis of the mid-hindbrain neuropore (MHNP) closure and revealed unexpected collective behavior of cells surrounding the MHNP. The cells first gathered to the closing point and subsequently relocated as if they were released from the point. Inhibition of caspases or matrix metalloproteases with chemical inhibitors impaired the cell relocation.

Conclusions: These lines of evidence suggest that apoptosis-mediated degradation of extracellular matrix might facilitate the final process of neuropore closure.

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半胱天冬酶和基质金属蛋白酶促进后脑神经孔关闭后非神经外胚层的集体行为。
背景:哺乳动物的大脑是通过神经管闭合(NTC)形成的,其中两个相对的神经褶皱脊在中线融合,并在神经管顶板和上覆的非神经外胚层中重塑。细胞凋亡在神经嵴NTC开始时就被广泛观察到,对NTC的正常发展至关重要,但其在NTC关闭后的作用尚不清楚。结果:在这里,我们对中后脑神经孔(MHNP)闭合进行了实时成像分析,并揭示了MHNP周围细胞的意外集体行为。细胞首先聚集到闭合点,然后重新定位,就好像它们从该点被释放一样。用化学抑制剂抑制半胱天蛋白酶或基质金属蛋白酶会损害细胞的重新定位。结论:这些证据表明,细胞凋亡介导的细胞外基质降解可能促进神经孔关闭的最终过程。
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BMC Developmental Biology
BMC Developmental Biology 生物-发育生物学
自引率
0.00%
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0
审稿时长
>12 weeks
期刊介绍: BMC Developmental Biology is an open access, peer-reviewed journal that considers articles on the development, growth, differentiation and regeneration of multicellular organisms, including molecular, cellular, tissue, organ and whole organism research.
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