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骨髓龛稳态中的自噬介体

Autophagic Mediators in Bone Marrow Niche Homeostasis.

机构信息

School of Biosciences and Veterinary Medicine, University of Camerino, Camerino, MC, Italy.

出版信息

Adv Exp Med Biol. 2022;1376:61-75. doi: 10.1007/5584_2021_666.

DOI:10.1007/5584_2021_666
PMID:34480334
Abstract

The bone marrow serves as a reservoir for a multifunctional assortment of stem, progenitor, and mature cells, located in functional anatomical micro-areas termed niches. Within the niche, hematopoietic and mesenchymal progenies establish a symbiotic relationship characterized by interdependency and interconnectedness. The fine-tuned physical and molecular interactions that occur in the niches guarantee physiological bone turnover, blood cell maturation and egression, and moderation of inflammatory and oxidative intramural stressful conditions. The disruption of bone marrow niche integrity causes severe local and systemic pathological settings, and thus bone marrow inhabitants have been the object of extensive study. In this context, research has revealed the importance of the autophagic apparatus for niche homeostatic maintenance. Archetypal autophagic players such as the p62 and the Atg family proteins have been found to exert a variety of actions, some autophagy-related and others not; they moderate the essential features of mesenchymal and hematopoietic stem cells and switch their operational schedules. This chapter focuses on our current understanding of bone marrow functionality and the role of the executive autophagic apparatus in the niche framework. Autophagic mediators such as p62 and Atg7 are currently considered the most important orchestrators of stem and mature cell dynamics in the bone marrow.

摘要

骨髓作为一个多功能的干细胞、祖细胞和成熟细胞的储库,位于功能解剖微区,称为龛。在龛内,造血和间充质祖细胞建立了一种共生关系,其特征是相互依存和相互联系。龛内发生的精细的物理和分子相互作用保证了生理骨转换、血细胞成熟和迁出以及炎症和氧化腔内应激条件的调节。骨髓龛完整性的破坏会导致严重的局部和全身病理状态,因此骨髓居民一直是广泛研究的对象。在这方面,研究揭示了自噬装置对于龛稳态维持的重要性。典型的自噬参与者,如 p62 和 Atg 家族蛋白,被发现具有多种作用,有些与自噬有关,有些则没有;它们调节间充质和造血干细胞的基本特征,并改变它们的操作时间表。本章重点介绍我们对骨髓功能的当前理解以及执行自噬装置在龛框架中的作用。自噬介质,如 p62 和 Atg7,目前被认为是骨髓中干细胞和成熟细胞动力学的最重要的协调者。

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Autophagic Mediators in Bone Marrow Niche Homeostasis.骨髓龛稳态中的自噬介体
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The bone marrow niche: habitat to hematopoietic and mesenchymal stem cells, and unwitting host to molecular parasites.骨髓生态位:造血干细胞和间充质干细胞的栖息地,以及分子寄生虫的不知情宿主。
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本文引用的文献

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Archetypal autophagic players through new lenses for bone marrow stem/mature cells regulation.透过新视角看待骨髓干细胞/成熟细胞调节中的典型自噬分子。
J Cell Physiol. 2021 Sep;236(9):6101-6114. doi: 10.1002/jcp.30296. Epub 2021 Jan 25.
2
Loss of p62 impairs bone turnover and inhibits PTH-induced osteogenesis.p62 的缺失会损害骨转换并抑制 PTH 诱导的成骨作用。
J Cell Physiol. 2020 Oct;235(10):7516-7529. doi: 10.1002/jcp.29654. Epub 2020 Feb 26.
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Live-animal imaging of native haematopoietic stem and progenitor cells.活体内示踪造血干/祖细胞。
自噬之外的P62/SQSTM1:在实验动物和家畜中的生理作用及治疗应用
Life (Basel). 2022 Apr 6;12(4):539. doi: 10.3390/life12040539.
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Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells.功能不同的Mx1+αSMA+骨膜骨骼干细胞的鉴定
Cell Stem Cell. 2019 Dec 5;25(6):784-796.e5. doi: 10.1016/j.stem.2019.11.003.
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Autophagy in bone homeostasis and the onset of osteoporosis.自噬在骨稳态及骨质疏松症发病中的作用
Bone Res. 2019 Oct 3;7:28. doi: 10.1038/s41413-019-0058-7. eCollection 2019.
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Mesenchymal stem versus stromal cells: International Society for Cell & Gene Therapy (ISCT®) Mesenchymal Stromal Cell committee position statement on nomenclature.间质干细胞与基质细胞:国际细胞与基因治疗学会(ISCT®)间质干细胞委员会关于命名的立场声明。
Cytotherapy. 2019 Oct;21(10):1019-1024. doi: 10.1016/j.jcyt.2019.08.002. Epub 2019 Sep 13.
7
Loss of autophagy in chondrocytes causes severe growth retardation.软骨细胞中的自噬缺失会导致严重的生长迟缓。
Autophagy. 2020 Mar;16(3):501-511. doi: 10.1080/15548627.2019.1628541. Epub 2019 Jun 16.
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Autophagy: a potential key contributor to the therapeutic action of mesenchymal stem cells.自噬:间充质干细胞治疗作用的潜在关键贡献者。
Autophagy. 2020 Jan;16(1):28-37. doi: 10.1080/15548627.2019.1630223. Epub 2019 Jun 18.
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Adrenergic Modulation of Hematopoiesis.造血作用的肾上腺素能调节
J Neuroimmune Pharmacol. 2020 Mar;15(1):82-92. doi: 10.1007/s11481-019-09840-7. Epub 2019 Feb 14.
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Haematopoietic stem cell activity and interactions with the niche.造血干细胞活性及其与龛位的相互作用。
Nat Rev Mol Cell Biol. 2019 May;20(5):303-320. doi: 10.1038/s41580-019-0103-9.