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

• Published in: BMC developmental biology 2018-07, Vol.18 (1), p.17-17, Article 17
• Main Authors: Shinotsuka, Naomi, Yamaguchi, Yoshifumi, Nakazato, Kenichi, Matsumoto, Yudai, Mochizuki, Atsushi, Miura, Masayuki
• Format: Article
• Language: English
• Subjects: Amino Acid Chloromethyl Ketones - pharmacology; Animals; Apoptosis; Caspases; Caspases - metabolism; Cell regulation; Cell Shape - drug effects; Chemical properties; Cytological research; Ectoderm; Ectoderm - cytology; Ectoderm - embryology; Ectoderm - enzymology; Extracellular matrix; Hindbrain; Insects; Mammals; Matrix Metalloproteinases - metabolism; Mice, Transgenic; Morphogenesis; Morphology; Movement; Neural Crest - embryology; Neural tube; Neural Tube - cytology; Neural Tube - embryology; Neuroimaging; Properties; Proteases; Relocation; Rhombencephalon - embryology
• ISSN: 1471-213X; 1471-213X
• DOI: 10.1186/s12861-018-0175-3

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