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在人骨髓基质细胞集落中鉴定出具有快速自我更新能力和多能性的成体干细胞亚群。

Identification of a subpopulation of rapidly self-renewing and multipotential adult stem cells in colonies of human marrow stromal cells.

作者信息

Colter D C, Sekiya I, Prockop D J

机构信息

Center for Gene Therapy, Tulane University Health Sciences Center, 1430 Tulane Avenue SL-99, New Orleans, LA 70112, USA.

出版信息

Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7841-5. doi: 10.1073/pnas.141221698. Epub 2001 Jun 26.

Abstract

Marrow stromal cells are adult stem cells from bone marrow that can differentiate into multiple nonhematopoietic cell lineages. Previous reports demonstrated that single-cell-derived colonies of marrow stromal cells contained two morphologically distinct cell types: spindle-shaped cells and large flat cells. Here we found that early colonies also contain a third kind of cell: very small round cells that rapidly self-renew. Samples enriched for the small cells had a greater potential for multipotential differentiation than samples enriched for the large cells. Also, the small cells expressed a series of surface epitopes and other proteins that potentially can be used to distinguish the small cells from the large cells. The results suggested it will be important to distinguish the major subpopulations of marrow stromal cells in defining their biology and their potential for cell and gene therapy.

摘要

骨髓基质细胞是来自骨髓的成体干细胞,能够分化为多种非造血细胞谱系。先前的报告表明,单细胞来源的骨髓基质细胞集落包含两种形态上不同的细胞类型:纺锤形细胞和大扁平细胞。在这里,我们发现早期集落还包含第三种细胞:能够快速自我更新的非常小的圆形细胞。富含小细胞的样本比富含大细胞的样本具有更大的多能分化潜力。此外,小细胞表达了一系列表面表位和其他蛋白质,这些蛋白质有可能用于区分小细胞和大细胞。结果表明,在定义骨髓基质细胞的生物学特性及其细胞和基因治疗潜力时,区分其主要亚群将非常重要。

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Mesenchymal stem cells and gene therapy.
Clin Orthop Relat Res. 2000 Oct(379 Suppl):S67-70. doi: 10.1097/00003086-200010001-00010.
2
Spinal cord injury in rat: treatment with bone marrow stromal cell transplantation.
Neuroreport. 2000 Sep 11;11(13):3001-5. doi: 10.1097/00001756-200009110-00035.
3
Adult rat and human bone marrow stromal cells differentiate into neurons.成年大鼠和人类骨髓基质细胞可分化为神经元。
J Neurosci Res. 2000 Aug 15;61(4):364-70. doi: 10.1002/1097-4547(20000815)61:4<364::AID-JNR2>3.0.CO;2-C.

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