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干细胞与细胞身份的演变概念

Stem cells and the evolving notion of cellular identity.

作者信息

Daley George Q

机构信息

Stem Cell Transplantation Program, Division of Hematology/Oncology, Howard Hughes Medical Institute, Boston Children's Hospital and Dana Farber Cancer Institute, Boston, MA 02115, USA Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA

出版信息

Philos Trans R Soc Lond B Biol Sci. 2015 Oct 19;370(1680):20140376. doi: 10.1098/rstb.2014.0376.

DOI:10.1098/rstb.2014.0376
PMID:26416685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4634003/
Abstract

Stem cells are but one class of the myriad types of cells within an organism. With potential to self-renew and capacity to differentiate, stem cells play essential roles at multiple stages of development. In the early embryo, pluripotent stem cells represent progenitors for all tissues while later in development, tissue-restricted stem cells give rise to cells with highly specialized functions. As best understood in the blood, skin and gut, stem cells are the seeds that sustain tissue homeostasis and regeneration, while in other tissues like the muscle, liver, kidney and lung, various stem or progenitor cells play facultative roles in tissue repair and response to injury. Here, I will provide a brief perspective on the evolving notion of cellular identity and how reprogramming and transcription factor-mediated conversions of one cell type into another have fundamentally altered our assumptions about the stability of cell identity, with profound long-term implications for biomedical research and regenerative medicine.

摘要

干细胞只是生物体内无数类型细胞中的一类。干细胞具有自我更新的潜力和分化的能力,在发育的多个阶段发挥着重要作用。在早期胚胎中,多能干细胞是所有组织的祖细胞,而在发育后期,组织限制性干细胞产生具有高度特化功能的细胞。正如在血液、皮肤和肠道中所熟知的那样,干细胞是维持组织稳态和再生的种子,而在肌肉、肝脏、肾脏和肺等其他组织中,各种干细胞或祖细胞在组织修复和损伤反应中发挥着辅助作用。在此,我将简要阐述细胞身份这一不断演变的概念,以及重编程和转录因子介导的一种细胞类型向另一种细胞类型的转化如何从根本上改变了我们对细胞身份稳定性的假设,这对生物医学研究和再生医学具有深远的长期影响。

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本文引用的文献

1
Mapping the route from naive pluripotency to lineage specification.描绘从幼稚多能性到细胞谱系特化的路径。
Philos Trans R Soc Lond B Biol Sci. 2014 Dec 5;369(1657). doi: 10.1098/rstb.2013.0540.
2
CellNet: network biology applied to stem cell engineering.细胞网络:应用于干细胞工程的网络生物学
Cell. 2014 Aug 14;158(4):903-915. doi: 10.1016/j.cell.2014.07.020.
3
Dissecting engineered cell types and enhancing cell fate conversion via CellNet.通过CellNet剖析工程细胞类型并增强细胞命运转变。
Cell. 2014 Aug 14;158(4):889-902. doi: 10.1016/j.cell.2014.07.021.
4
Human embryonic stem cells derived by somatic cell nuclear transfer.体细胞核移植技术衍生的人类胚胎干细胞。
Cell. 2013 Jun 6;153(6):1228-38. doi: 10.1016/j.cell.2013.05.006. Epub 2013 May 15.
5
Origins and implications of pluripotent stem cell variability and heterogeneity.多能干细胞变异性和异质性的起源和意义。
Nat Rev Mol Cell Biol. 2013 Jun;14(6):357-68. doi: 10.1038/nrm3584. Epub 2013 May 15.
6
Small molecules, big roles -- the chemical manipulation of stem cell fate and somatic cell reprogramming.小分子,大作用——化学操纵干细胞命运和体细胞重编程。
J Cell Sci. 2012 Dec 1;125(Pt 23):5609-20. doi: 10.1242/jcs.096032.
7
A blueprint for engineering cell fate: current technologies to reprogram cell identity.细胞命运工程蓝图:重编程细胞身份的当前技术。
Cell Res. 2013 Jan;23(1):33-48. doi: 10.1038/cr.2013.1. Epub 2013 Jan 1.
8
The transcriptional and epigenomic foundations of ground state pluripotency.胚胎干细胞多能性的转录和表观遗传基础。
Cell. 2012 Apr 27;149(3):590-604. doi: 10.1016/j.cell.2012.03.026.
9
Accessing naïve human pluripotency.获取原始人类多能性。
Curr Opin Genet Dev. 2012 Jun;22(3):272-82. doi: 10.1016/j.gde.2012.03.001. Epub 2012 Mar 29.
10
CCAAT/enhancer binding protein alpha (C/EBP(alpha))-induced transdifferentiation of pre-B cells into macrophages involves no overt retrodifferentiation.CCAAT/增强子结合蛋白α(C/EBPα)诱导前 B 细胞向巨噬细胞的转分化不涉及明显的逆行分化。
Proc Natl Acad Sci U S A. 2011 Oct 11;108(41):17016-21. doi: 10.1073/pnas.1112169108. Epub 2011 Oct 3.