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本文引用的文献

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Energy metabolism in nuclear reprogramming.能量代谢与核重编程。
Biomark Med. 2011 Dec;5(6):715-29. doi: 10.2217/bmm.11.87.
2
UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells.UCP2 调节人多能干细胞的能量代谢和分化潜能。
EMBO J. 2011 Nov 15;30(24):4860-73. doi: 10.1038/emboj.2011.401.
3
The metabolome of induced pluripotent stem cells reveals metabolic changes occurring in somatic cell reprogramming.诱导多能干细胞的代谢组学揭示了体细胞重编程过程中发生的代谢变化。
Cell Res. 2012 Jan;22(1):168-77. doi: 10.1038/cr.2011.177. Epub 2011 Nov 8.
4
The permeability transition pore controls cardiac mitochondrial maturation and myocyte differentiation.通透性转换孔控制心脏线粒体成熟和心肌细胞分化。
Dev Cell. 2011 Sep 13;21(3):469-78. doi: 10.1016/j.devcel.2011.08.008.
5
Heart development: mitochondria in command of cardiomyocyte differentiation.心脏发育：线粒体指挥心肌细胞分化。
Dev Cell. 2011 Sep 13;21(3):392-3. doi: 10.1016/j.devcel.2011.08.021.
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Somatic oxidative bioenergetics transitions into pluripotency-dependent glycolysis to facilitate nuclear reprogramming.体细胞氧化生物能学转变为依赖多能性的糖酵解，以促进核重编程。
Cell Metab. 2011 Aug 3;14(2):264-71. doi: 10.1016/j.cmet.2011.06.011.
7
Anaerobicizing into pluripotency.将厌氧转化为多能性。
Cell Metab. 2011 Aug 3;14(2):143-4. doi: 10.1016/j.cmet.2011.07.003.
8
Regenerative medicine: on the vanguard of health care.再生医学：处于医疗保健的前沿。
Mayo Clin Proc. 2011 Jul;86(7):600-2. doi: 10.4065/mcp.2011.0325.
9
Bioenergetics, mitochondria, and cardiac myocyte differentiation.生物能量学、线粒体与心肌细胞分化
Prog Pediatr Cardiol. 2011 May;31(2):75-81. doi: 10.1016/j.ppedcard.2011.02.002.
10
Developmental enhancement of adenylate kinase-AMPK metabolic signaling axis supports stem cell cardiac differentiation.发育增强腺嘌呤激酶-AMPK 代谢信号轴支持干细胞心脏分化。
PLoS One. 2011 Apr 27;6(4):e19300. doi: 10.1371/journal.pone.0019300.

线粒体控制细胞命运。

Mitochondria in control of cell fate.

机构信息

Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Circ Res. 2012 Feb 17;110(4):526-9. doi: 10.1161/RES.0b013e31824ae5c1.

DOI:10.1161/RES.0b013e31824ae5c1
PMID:22343555
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3491643/
Abstract

The behavior of the mitochondrial permeability transition pore has been linked to mitochondrial maturation underlying cardiomyocyte differentiation in the embryo. Mitochondrial signaling in heart development has direct implications for cardiogenesis and stem cell lineage specification.

摘要

线粒体通透性转换孔的行为与胚胎中心肌细胞分化所涉及的线粒体成熟有关。心脏发育中的线粒体信号转导对心脏发生和干细胞谱系特化有直接影响。