Nardi Nance Beyer, Camassola Melissa
Programa de Pós-Graduação em Diagnóstico Genético e Molecular, Universidade Luterana do Brasil, Canoas, RS, Brazil.
Methods Mol Biol. 2011;698:151-60. doi: 10.1007/978-1-60761-999-4_12.
Initial attempts to cultivate mesenchymal stem cells (MSCs) were more successful from human than murine tissues. Methods for the in vitro expansion of murine MSCs were described more recently, but are now well established. Despite limitations such as a poor equivalence to be expected between cultured stem cells and their in vivo counterparts, MSC culture allows the expansion of a cell population capable of providing important information on the biology of stem cells and their therapeutic application. Murine MSCs may be obtained from the bone marrow and virtually from any other organ or tissue. This chapter describes the most widely used method, which involves the preparation of single-cell suspension followed by incubation for 1-3 days and removal of nonadherent cells. The adherent fraction is then expanded by continuous culture and may be maintained for prolonged periods of time.
最初从人组织中培养间充质干细胞(MSC)比从鼠组织中培养更成功。鼠MSC体外扩增方法是最近才描述的,但现在已得到充分确立。尽管存在局限性,如培养的干细胞与其体内对应物之间预期的等效性较差,但MSC培养允许扩增一个细胞群体,该群体能够提供有关干细胞生物学及其治疗应用的重要信息。鼠MSC可从骨髓以及几乎任何其他器官或组织中获得。本章描述了最广泛使用的方法,该方法包括制备单细胞悬液,然后孵育1 - 3天并去除非贴壁细胞。然后通过连续培养扩增贴壁部分,并且可以长时间维持。