Wnt Signaling and Its Impact on Mitochondrial and Cell Cycle Dynamics in Pluripotent Stem Cells

被引:42
作者
Rasmussen, Megan L. [1 ]
Ortolano, Natalya A. [1 ]
Romero-Morales, Alejandra I. [1 ]
Gama, Vivian [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Vanderbilt Ctr Stem Cell Biol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
关键词
stem cells; pluripotency; mitochondria; cell cycle; apoptosis; Wnt; MITOTIC SPINDLE ORIENTATION; SELF-RENEWAL; BETA-CATENIN; METABOLIC-REGULATION; INDUCED APOPTOSIS; ASYMMETRIC DIVISION; HIPPOCAMPAL-NEURONS; NEURAL PROGENITORS; FRIZZLED HOMOLOGS; CORTICAL-NEURONS;
D O I
10.3390/genes9020109
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The core transcriptional network regulating stem cell self-renewal and pluripotency remains an intense area of research. Increasing evidence indicates that modified regulation of basic cellular processes such as mitochondrial dynamics, apoptosis, and cell cycle are also essential for pluripotent stem cell identity and fate decisions. Here, we review evidence for Wnt regulation of pluripotency and self-renewal, and its connections to emerging features of pluripotent stem cells, including (1) increased mitochondrial fragmentation, (2) increased sensitivity to cell death, and (3) shortened cell cycle. We provide a general overview of the stem cell-specific mechanisms involved in the maintenance of these uncharacterized hallmarks of pluripotency and highlight potential links to the Wnt signaling pathway. Given the physiological importance of stem cells and their enormous potential for regenerative medicine, understanding fundamental mechanisms mediating the crosstalk between Wnt, organelle-dynamics, apoptosis, and cell cycle will be crucial to gain insight into the regulation of stemness.
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页数:24
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