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一种支持成年小胶质细胞增殖并维持其静息状态的培养系统的开发。

Development of a culture system that supports adult microglial cell proliferation and maintenance in the resting state.

作者信息

Ponomarev Eugene D, Novikova Marina, Maresz Katarzyna, Shriver Leah P, Dittel Bonnie N

机构信息

Blood Research Institute, Blood Center of Southeastern Wisconsin, P.O. Box 2178, Milwaukee, WI 53201-2178, USA.

出版信息

J Immunol Methods. 2005 May;300(1-2):32-46. doi: 10.1016/j.jim.2005.02.011. Epub 2005 Apr 26.

Abstract

Microglial cells constitute what is considered to be a fixed macrophage population in the central nervous system (CNS), which are broadly implicated in the regulation of neuroinflammation. In the normal adult CNS, microglial cells exist in a resting state characterized by a minimal or negative expression of MHC class II and the co-stimulatory molecules CD80, CD86 and CD40 and exhibit a unique ramified morphology. Microglial cell activation is associated with many inflammatory and neurogenerative CNS pathologies and is characterized by the transformation of resting microglia into cells with a macrophage morphology and up-regulation of MHC class II and co-stimulatory molecules. The cellular and molecular mechanisms required for microglial cell activation and their immunological functions in the adult brain still remain enigmatic, primarily due to the lack of an appropriate culture system that both facilitates microglial survival and expansion in the resting state. Here, we describe a new M-CSF-dependent culture system that overcomes these barriers and allows the long-term proliferation and maintenance of resting adult microglial cells isolated from the CNS. These cultured microglial cells retain their plasticity as indicated by their ability to up-regulate MHC class II and differentiate into cells with a macrophage morphology following the addition of IFN-gamma and GM-CSF, or activated T cells, which produce both cytokines. By measuring the proliferation of the T cells, we were also able to demonstrate that the microglial cells differentiated into fully functional antigen presenting cells. In addition, the replacement of the M-CSF with GM-CSF resulted in the differentiation of microglial cells into cells morphologically and phenotypically similar to dendritic cells. Our microglial cell culture system is the first described that allows the expansion of adult cells in the resting state and will facilitate studies examining the specific mechanisms of microglial cell activation and functions involved in a variety of CNS pathologies.

摘要

小胶质细胞构成了中枢神经系统(CNS)中被认为是固定的巨噬细胞群体,广泛参与神经炎症的调节。在正常成年中枢神经系统中,小胶质细胞处于静息状态,其特征是MHC II类分子以及共刺激分子CD80、CD86和CD40的表达极少或呈阴性,并呈现独特的分支形态。小胶质细胞活化与许多炎症性和神经退行性中枢神经系统疾病相关,其特征是静息小胶质细胞转变为具有巨噬细胞形态的细胞,并上调MHC II类分子和共刺激分子。小胶质细胞活化所需的细胞和分子机制及其在成人大脑中的免疫功能仍然不明,主要是因为缺乏一种既有利于小胶质细胞在静息状态下存活和扩增的合适培养系统。在此,我们描述了一种新的依赖M-CSF的培养系统,该系统克服了这些障碍,并允许从CNS分离的成年静息小胶质细胞长期增殖和维持。这些培养的小胶质细胞保持了它们的可塑性,这体现在添加IFN-γ和GM-CSF或活化T细胞(产生这两种细胞因子)后,它们上调MHC II类分子并分化为具有巨噬细胞形态的细胞的能力上。通过测量T细胞的增殖,我们还能够证明小胶质细胞分化为功能完全的抗原呈递细胞。此外,用GM-CSF替代M-CSF导致小胶质细胞分化为形态和表型与树突状细胞相似的细胞。我们的小胶质细胞培养系统是首次描述的允许成年静息状态细胞扩增的系统,将有助于研究小胶质细胞活化的具体机制以及参与各种中枢神经系统疾病的功能。

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