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本文引用的文献

1
T Helper Cell Cytokines Modulate Intestinal Stem Cell Renewal and Differentiation.辅助性 T 细胞细胞因子调节肠道干细胞的更新和分化。
Cell. 2018 Nov 15;175(5):1307-1320.e22. doi: 10.1016/j.cell.2018.10.008. Epub 2018 Nov 1.
2
Allergic inflammatory memory in human respiratory epithelial progenitor cells.人类呼吸道上皮祖细胞中的过敏炎症记忆。
Nature. 2018 Aug;560(7720):649-654. doi: 10.1038/s41586-018-0449-8. Epub 2018 Aug 22.
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Notch ligand Dll1 mediates cross-talk between mammary stem cells and the macrophageal niche.Notch 配体 Dll1 介导乳腺干细胞与巨噬细胞生态位之间的串扰。
Science. 2018 Jun 29;360(6396). doi: 10.1126/science.aan4153. Epub 2018 May 17.
4
A Circular RNA Protects Dormant Hematopoietic Stem Cells from DNA Sensor cGAS-Mediated Exhaustion.环状 RNA 保护休眠造血干细胞免受 DNA 传感器 cGAS 介导的耗竭。
Immunity. 2018 Apr 17;48(4):688-701.e7. doi: 10.1016/j.immuni.2018.03.016. Epub 2018 Apr 3.
5
The role of CSF1R-dependent macrophages in control of the intestinal stem-cell niche.CSF1R 依赖性巨噬细胞在肠道干细胞龛调控中的作用。
Nat Commun. 2018 Mar 28;9(1):1272. doi: 10.1038/s41467-018-03638-6.
6
Quiescent Tissue Stem Cells Evade Immune Surveillance.静止组织干细胞逃避免疫监视。
Immunity. 2018 Feb 20;48(2):271-285.e5. doi: 10.1016/j.immuni.2018.02.001.
7
CD150 Bone Marrow Tregs Maintain Hematopoietic Stem Cell Quiescence and Immune Privilege via Adenosine.CD150+ 骨髓 Tregs 通过腺苷维持造血干细胞静止和免疫豁免。
Cell Stem Cell. 2018 Mar 1;22(3):445-453.e5. doi: 10.1016/j.stem.2018.01.017. Epub 2018 Feb 15.
8
BCG Educates Hematopoietic Stem Cells to Generate Protective Innate Immunity against Tuberculosis.BCG 可教育造血干细胞产生针对结核病的保护性先天免疫。
Cell. 2018 Jan 11;172(1-2):176-190.e19. doi: 10.1016/j.cell.2017.12.031.
9
Western Diet Triggers NLRP3-Dependent Innate Immune Reprogramming.西式饮食引发 NLRP3 依赖性固有免疫重编程。
Cell. 2018 Jan 11;172(1-2):162-175.e14. doi: 10.1016/j.cell.2017.12.013.
10
Modulation of Myelopoiesis Progenitors Is an Integral Component of Trained Immunity.骨髓造血祖细胞的调节是训练免疫的一个组成部分。
Cell. 2018 Jan 11;172(1-2):147-161.e12. doi: 10.1016/j.cell.2017.11.034.

二人为舞:免疫与干细胞在健康与疾病中的对话。

Two to Tango: Dialog between Immunity and Stem Cells in Health and Disease.

机构信息

Robin Chemers Neustein Laboratory of Mammalian Cell Biology and Development, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.

Robin Chemers Neustein Laboratory of Mammalian Cell Biology and Development, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10065, USA.

出版信息

Cell. 2018 Nov 1;175(4):908-920. doi: 10.1016/j.cell.2018.08.071.

DOI:10.1016/j.cell.2018.08.071
PMID:30388451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6294328/
Abstract

Stem cells regenerate tissues in homeostasis and under stress. By taking cues from their microenvironment or "niche," they smoothly transition between these states. Immune cells have surfaced as prominent members of stem cell niches across the body. Here, we draw parallels between different stem cell niches to explore the context-specific interactions that stem cells have with tissue-resident and recruited immune cells. We also highlight stem cells' innate ability to sense and respond to stress and the enduring memory that forms from such encounters. This fascinating crosstalk holds great promise for novel therapies in inflammatory diseases and regenerative medicine.

摘要

干细胞在体内平衡和应激状态下再生组织。通过从其微环境或“生态位”中获取线索,它们可以在这些状态之间顺利转换。免疫细胞已经成为全身干细胞生态位中突出的成员。在这里,我们将不同的干细胞生态位进行对比,以探讨干细胞与组织驻留和募集的免疫细胞之间的特定于环境的相互作用。我们还强调了干细胞感知和应对应激的固有能力,以及由此产生的持久记忆。这种引人入胜的串扰为炎症性疾病和再生医学的新疗法带来了巨大的希望。