从鼠脑中分离和定位于血管周围的间充质干细胞。
Isolation and perivascular localization of mesenchymal stem cells from mouse brain.
机构信息
Department of Neurosurgery, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030-4009, USA.
出版信息
Neurosurgery. 2010 Sep;67(3):711-20. doi: 10.1227/01.NEU.0000377859.06219.78.
BACKGROUND
Although originally isolated from the bone marrow, mesenchymal stem cells (MSCs) have recently been detected in other tissues. However, little is known about MSCs in the brain.
OBJECTIVE
To determine the extent to which cells with the features of MSCs exist in normal brain tissue and to determine the location of these cells in the brain.
METHODS
Single-cell suspensions from mouse brains were cultured according to the same methods used for culturing bone marrow-derived MSCs (BM-MSCs). These brain-derived cells were analyzed by fluorescence-activated cell sorting for surface markers associated with BM-MSCs (stem cell antigen 1 [Sca-1+], CD9+, CD45-, CD11b-, and CD31-). Brain-derived cells were exposed to mesenchymal differentiation conditions. To determine the locations of these cells within the brain, sections of normal brains were analyzed by immunostaining for Sca-1, CD31, and nerve/glial antigen 2.
RESULTS
Cells morphologically similar to mouse BM-MSCs were identified and called brain-derived MSCs (Br-MSCs). Fluorescence-activated cell sorting indicated that the isolated cells had a surface marker profile similar to BM-MSCs, ie, Sca-1V+, CD9+, CD45-, and CD11b-. Like BM-MSCs, Br-MSCs were capable of differentiation into adipocytes, osteocytes, and chondrocytes. Immunostaining indicated that Sca-1+ Br-MSCs are located around blood vessels and may represent progenitor cells that serve as a source of mesenchymal elements (eg, pericytes) within the brain.
CONCLUSION
Our results indicate that cells similar to BM-MSCs exist in the brain. These Br-MSCs appear to be located within the vascular niche and may provide the mesenchymal elements of this niche. Because MSCs may be part of the cellular response to tissue injury, Br-MSCs may represent targets in the therapy of pathological processes such as stroke, trauma, and tumorigenesis.
背景
间充质干细胞(MSCs)最初虽分离自骨髓,但近来在其他组织中也发现了 MSCs。然而,关于脑内 MSCs 的信息却知之甚少。
目的
明确具有 MSCs 特征的细胞在正常脑组织中的存在程度,并确定这些细胞在脑内的位置。
方法
根据培养骨髓来源的 MSCs(BM-MSCs)的相同方法,培养来自小鼠脑的单细胞悬液。通过荧光激活细胞分选分析与 BM-MSCs 相关的表面标志物(干细胞抗原 1 [Sca-1+]、CD9+、CD45-、CD11b-和 CD31-)对这些脑源性细胞进行分析。将脑源性细胞暴露于间充质分化条件下。为了确定这些细胞在脑内的位置,通过免疫染色分析正常脑切片中 Sca-1、CD31 和神经胶质抗原 2 的位置。
结果
鉴定出形态上类似于小鼠 BM-MSCs 的细胞,并将其称为脑源性 MSCs(Br-MSCs)。荧光激活细胞分选表明,分离的细胞具有类似于 BM-MSCs 的表面标志物谱,即 Sca-1V+、CD9+、CD45-和 CD11b-。与 BM-MSCs 一样,Br-MSCs 能够分化为脂肪细胞、成骨细胞和软骨细胞。免疫染色表明,Sca-1+Br-MSCs 位于血管周围,可能代表脑内间充质成分(如周细胞)的祖细胞。
结论
我们的结果表明,脑内存在类似于 BM-MSCs 的细胞。这些 Br-MSCs 似乎位于血管龛位内,可能为该龛位的间充质成分提供来源。由于 MSCs 可能是组织损伤后细胞反应的一部分,因此 Br-MSCs 可能成为中风、创伤和肿瘤发生等病理过程治疗的靶点。