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从人外周血中分离出的造血干细胞和间充质干细胞的分化能力。

Differentiation ability of hematopoietic stem cells and mesenchymal stem cells isolated from human peripheral blood.

作者信息

Samundeshwari Echambadi Loganathan, Kattaru Surekha, Kodavala Sireesha, Chandrasekhar Chodimella, Sarma Potukuchi Venkata Gurunadha Krishna

机构信息

Department of Biotechnology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India.

Department of Hematology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India.

出版信息

Front Cell Dev Biol. 2024 Dec 18;12:1450543. doi: 10.3389/fcell.2024.1450543. eCollection 2024.

Abstract

Human hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs) are the major stem cells of the bone marrow and are usually isolated from the peripheral blood. In the present study, we isolated these stem cells by an apheresis method from a donor who was administered granulocyte colony-stimulating factor (G-CSF). propagation of these stem cells showed a plastic-adherence property expressing CD73 and CD105 surface markers, which is a characteristic feature of MSCs. HSCs are non-adherent cells growing as a suspension culture, expressing CD150, CD133, CD34, and CD45 on their surface, which regulate the quiescence nature, and they derive energy from anaerobic glycolysis. The HSCs grow slowly compared to MSCs, are more viable, and survive for long periods under conditions, which are due to the expression of telomerase, BCL2, and Notch1 genes. The poor viability of MSCs in the culture due to the prominent expression of apoptotic genes BAX, caspase-3, and caspase-9 leads to rapid apoptosis. This was evident even in cells (astrocytes, osteocytes, and beta cells of the islets of Langerhans) differentiated from HSCs and MSCs, thus highlighting the importance of HSCs, the naive stem cells, in regeneration of tissues.

摘要

人类造血干细胞(HSCs)和间充质干细胞(MSCs)是骨髓中的主要干细胞,通常从外周血中分离得到。在本研究中,我们通过单采术从一名接受粒细胞集落刺激因子(G-CSF)治疗的供体中分离出这些干细胞。这些干细胞的增殖表现出表达CD73和CD105表面标志物的贴壁特性,这是间充质干细胞的一个特征。造血干细胞是作为悬浮培养生长的非贴壁细胞,其表面表达CD150、CD133、CD34和CD45,这些标志物调节静止状态,并且它们通过无氧糖酵解获取能量。与间充质干细胞相比,造血干细胞生长缓慢,更具活力,并且在特定条件下能长期存活,这归因于端粒酶、BCL2和Notch1基因的表达。由于凋亡基因BAX、caspase-3和caspase-9的显著表达,间充质干细胞在培养中的活力较差,导致快速凋亡。这在从造血干细胞和间充质干细胞分化而来的细胞(星形胶质细胞、骨细胞和胰岛β细胞)中也很明显,从而突出了原始干细胞造血干细胞在组织再生中的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/11688275/519c376857bd/fcell-12-1450543-g001.jpg

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