Wölwer Christina B, Gödde Nathan, Pase Luke B, Elsum Imogen A, Lim Krystle Y B, Sacirbegovic Faruk, Walkley Carl R, Ellis Sarah, Ohno Shigeo, Matsuzaki Fumio, Russell Sarah M, Humbert Patrick O
Cell Cycle and Cancer Genetics, Peter MacCallum Cancer Centre, East Melbourne, Australia.
La Trobe Institute for Molecular Science, Department of Biochemistry and Genetics, La Trobe University, Melbourne, Australia.
PLoS One. 2017 Jan 17;12(1):e0170295. doi: 10.1371/journal.pone.0170295. eCollection 2017.
Erythroid enucleation is the process by which the future red blood cell disposes of its nucleus prior to entering the blood stream. This key event during red blood cell development has been likened to an asymmetric cell division (ACD), by which the enucleating erythroblast divides into two very different daughter cells of alternate molecular composition, a nucleated cell that will be removed by associated macrophages, and the reticulocyte that will mature to the definitive erythrocyte. Here we investigated gene expression of members of the Par, Scribble and Pins/Gpsm2 asymmetric cell division complexes in erythroid cells, and functionally tested their role in erythroid enucleation in vivo and ex vivo. Despite their roles in regulating ACD in other contexts, we found that these polarity regulators are not essential for erythroid enucleation, nor for erythroid development in vivo. Together our results put into question a role for cell polarity and asymmetric cell division in erythroid enucleation.
红细胞去核是未来的红细胞在进入血流之前处理其细胞核的过程。红细胞发育过程中的这一关键事件被比作不对称细胞分裂(ACD),通过这种分裂,正在去核的成红细胞分裂成两个分子组成截然不同的子细胞,一个有核细胞将被相关巨噬细胞清除,另一个网织红细胞将成熟为成熟红细胞。在这里,我们研究了Par、Scribble和Pins/Gpsm2不对称细胞分裂复合物成员在红细胞中的基因表达,并在体内和体外功能测试了它们在红细胞去核中的作用。尽管它们在其他情况下调节ACD发挥作用,但我们发现这些极性调节因子对于红细胞去核以及体内红细胞发育并非必不可少。我们的研究结果共同对细胞极性和不对称细胞分裂在红细胞去核中的作用提出了质疑。