Qiu Runxiang, Murai Kiyohito, Lu Qiang
Department of Developmental and Stem Cell Biology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.
Department of Macroscopic Anatomy, Nagasaki University Graduate School of Biomedical Sciences, 1-12-4 Sakamoto, Nagasaki 852-8523, Japan.
Cereb Cortex Commun. 2020;1(1):tgaa003. doi: 10.1093/texcom/tgaa003. Epub 2020 Feb 20.
It was proposed that similar to its role in the invertebrate nervous system, mitotic spindle orientation (or cell cleavage plane orientation) of a dividing neural progenitor cell specifies the fate of daughter cells in the mammalian brain, modulating the production of neurons via symmetric versus asymmetric cell divisions during the course of neurogenesis. Experimental tests of the sufficiency of spindle/cleavage plane orientation in mammalian cell fate determination have yielded conflicting results. On the other hand, the necessity of spindle/cleavage plane orientation in mammalian cell fate determination has not yet been addressed. Here we examined the necessity of spindle/cleavage plane orientation during cortical neurogenesis in mice with loss-of-function of the RGS3-KIF20A interaction axis. We present evidence that while inactivation of RGS3 or KIF20A was linked to a shift in neural progenitor cells from proliferative to differentiative divisions in the developing cortex, these genetic mutations did not lead to anticipated alteration in the orientation of spindle/cleavage plane. Our results indicate that the RGS3-KIF20A axis regulates the balance between proliferation and differentiation in the mammalian cortex employing a mechanism independent of spindle/cleavage plane orientation. These data also caution against using spindle/cleavage plane orientation as the synonym for cell fate determination.
有人提出,类似于其在无脊椎动物神经系统中的作用,正在分裂的神经祖细胞的有丝分裂纺锤体定向(或细胞分裂平面定向)决定了哺乳动物大脑中 daughter 细胞的命运,在神经发生过程中通过对称与不对称细胞分裂调节神经元的产生。关于纺锤体/分裂平面定向在哺乳动物细胞命运决定中的充分性的实验测试产生了相互矛盾的结果。另一方面,纺锤体/分裂平面定向在哺乳动物细胞命运决定中的必要性尚未得到探讨。在这里,我们研究了 RGS3-KIF20A 相互作用轴功能丧失的小鼠在皮质神经发生过程中纺锤体/分裂平面定向的必要性。我们提供的证据表明,虽然 RGS3 或 KIF20A 的失活与发育中的皮质中神经祖细胞从增殖性分裂向分化性分裂的转变有关,但这些基因突变并未导致纺锤体/分裂平面定向的预期改变。我们的结果表明,RGS3-KIF20A 轴采用一种独立于纺锤体/分裂平面定向的机制调节哺乳动物皮质中增殖与分化之间的平衡。这些数据也告诫不要将纺锤体/分裂平面定向用作细胞命运决定的同义词。