Koltowska Katarzyna, Lagendijk Anne Karine, Pichol-Thievend Cathy, Fischer Johanna C, Francois Mathias, Ober Elke A, Yap Alpha S, Hogan Benjamin M
Division of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Division of Genomics of Development and Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia; Division of Cell Biology and Molecular Medicine, Institute for Molecular Bioscience, The University of Queensland, St Lucia, QLD 4072, Australia.
Cell Rep. 2015 Dec 1;13(9):1828-41. doi: 10.1016/j.celrep.2015.10.055. Epub 2015 Nov 19.
Lymphatic vessels arise chiefly from preexisting embryonic veins. Genetic regulators of lymphatic fate are known, but how dynamic cellular changes contribute during the acquisition of lymphatic identity is not understood. We report the visualization of zebrafish lymphatic precursor cell dynamics during fate restriction. In the cardinal vein, cellular commitment is linked with the division of bipotential Prox1-positive precursor cells, which occurs immediately prior to sprouting angiogenesis. Following precursor division, identities are established asymmetrically in daughter cells; one daughter cell becomes lymphatic and progressively upregulates Prox1, and the other downregulates Prox1 and remains in the vein. Vegfc drives cell division and Prox1 expression in lymphatic daughter cells, coupling signaling dynamics with daughter cell fate restriction and precursor division.
淋巴管主要起源于已有的胚胎静脉。已知淋巴管命运的基因调控因子,但在获得淋巴管特性过程中动态细胞变化是如何起作用的尚不清楚。我们报道了斑马鱼淋巴管前体细胞在命运限制过程中的动态可视化。在主静脉中,细胞定向分化与双潜能Prox1阳性前体细胞的分裂相关,这种分裂发生在发芽血管生成之前。前体细胞分裂后,子细胞中不对称地建立细胞特性;一个子细胞成为淋巴管细胞并逐渐上调Prox1的表达,另一个则下调Prox1的表达并保留在静脉中。Vegfc驱动淋巴管子细胞的细胞分裂和Prox1表达,将信号动态与子细胞命运限制和前体细胞分裂联系起来。