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来自成年骨髓的造血祖细胞可分化为在新生小鼠大脑中表达少突胶质细胞抗原的细胞。

Haematopoietic progenitor cells from adult bone marrow differentiate into cells that express oligodendroglial antigens in the neonatal mouse brain.

作者信息

Bonilla Sonia, Alarcón Pedro, Villaverde Ramón, Aparicio Pedro, Silva Augusto, Martínez Salvador

机构信息

Instituto de Neurociencias, UMH-CSIC, Campus San Juan, Alicante, Spain.

出版信息

Eur J Neurosci. 2002 Feb;15(3):575-82. doi: 10.1046/j.1460-9568.2002.01895.x.

Abstract

Stem cells are self-renewable, pluripotent cells that, in adult life, proliferate by a characteristic asymmetric division in which one daughter cell is committed to differentiation whereas the other remains a stem cell. These cells are also characterized by their ability to differentiate into various cell types under heterotopic environmental influences. In the present study, we have explored the potential of adult haematopoietic bone marrow cells to differentiate into cells of oligodendroglial lineage under physiological, active myelinating conditions. We present evidence of generation of cells expressing oligodendroglial specific markers from a bone marrow subpopulation enriched on adult haematopoietic progenitor cells (CD117+) in vivo after intracerebral transplantation into the neonatal mouse brain. Our results suggest that adult bone marrow cells have the capacity to undergo differentiation from haematopoietic to oligodendroglial cells and add support the validity of bone marrow transplants as an alternative treatment for demyelinating diseases of the CNS including Multiple Sclerosis.

摘要

干细胞是自我更新的多能细胞,在成年期,通过一种典型的不对称分裂进行增殖,其中一个子细胞致力于分化,而另一个则保留为干细胞。这些细胞的特征还在于它们在异位环境影响下分化为各种细胞类型的能力。在本研究中,我们探讨了成年造血骨髓细胞在生理、活跃髓鞘形成条件下分化为少突胶质细胞谱系细胞的潜力。我们提供了证据,表明在将富含成年造血祖细胞(CD117+)的骨髓亚群脑内移植到新生小鼠脑内后,体内可产生表达少突胶质细胞特异性标志物的细胞。我们的结果表明,成年骨髓细胞有能力从造血细胞分化为少突胶质细胞,并进一步支持了骨髓移植作为包括多发性硬化症在内的中枢神经系统脱髓鞘疾病替代治疗方法的有效性。

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