Graduate School of Sciences and Technology for Innovation, Yamaguchi University, Yamaguchi 753-8511, Japan.
Institute of Food and Radiation Biology, AERE, Bangladesh Atomic Energy Commission, Savar, Dhaka-3787, Bangladesh.
Cells. 2020 Apr 23;9(4):1058. doi: 10.3390/cells9041058.
Wound repair of cell membrane is a vital physiological phenomenon. We examined wound repair in cells by using a laserporation, which we recently invented. We examined the influx of fluorescent dyes from the external medium and monitored the cytosolic Ca after wounding. The influx of Ca through the wound pore was essential for wound repair. Annexin and ESCRT components accumulated at the wound site upon wounding as previously described in animal cells, but these were not essential for wound repair in cells. We discovered that calmodulin accumulated at the wound site upon wounding, which was essential for wound repair. The membrane accumulated at the wound site to plug the wound pore by two-steps, depending on Ca influx and calmodulin. From several lines of evidence, the membrane plug was derived from de novo generated vesicles at the wound site. Actin filaments also accumulated at the wound site, depending on Ca influx and calmodulin. Actin accumulation was essential for wound repair, but microtubules were not essential. A molecular mechanism of wound repair will be discussed.
细胞膜的伤口修复是一种重要的生理现象。我们使用最近发明的激光穿孔法来研究细胞的伤口修复。我们观察了荧光染料从外部介质中的流入,并监测了伤口后的细胞质钙离子。通过伤口孔的钙离子流入对于伤口修复是必不可少的。正如在动物细胞中所描述的那样,在伤口部位,膜联蛋白和 ESCRT 成分的积累,但这些对于 细胞的伤口修复并不是必需的。我们发现,钙调蛋白在伤口部位积累,这对于伤口修复是必需的。膜在伤口部位的积累通过两步来堵塞伤口孔,这取决于钙离子流入和钙调蛋白。从几个证据来看,膜塞是由伤口部位新生成的囊泡衍生而来的。肌动蛋白丝也在伤口部位积累,这取决于钙离子流入和钙调蛋白。肌动蛋白的积累对于伤口修复是必需的,但微管不是必需的。将讨论伤口修复的分子机制。