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B 细胞谱系定向的体外模型。

In-vitro models of B-lineage commitment.

作者信息

Kee B L, Paige C J

机构信息

Wellesley Hospital Research Institute, University of Toronto, Canada.

出版信息

Semin Immunol. 1995 Jun;7(3):143-54. doi: 10.1016/1044-5323(95)90042-x.

DOI:10.1016/1044-5323(95)90042-x
PMID:7579201
Abstract

The development of mature B lymphocytes from multipotent progenitors follows a pathway of differentiation marked by a progressive restriction in lineage options. The requirements for progression through the B lineage developmental pathway have been investigated intensively and a number of critical components of the differentiation process have been identified. However, the genetic basis for lineage determination remains unresolved. Recently, a number of in-vitro assays have been established which support the development of committed B cell progenitors from multipotent cells. These assays have provided a novel system in which the process of B lineage commitment can be followed and manipulated. In this review we present a model of B-lineage progression from multipotent progenitors to committed B-cell progenitors and discuss potential mediators of the commitment process.

摘要

多能祖细胞发育为成熟B淋巴细胞遵循一条分化途径,其特征是谱系选择逐渐受到限制。人们对通过B谱系发育途径的进展要求进行了深入研究,并确定了分化过程中的一些关键成分。然而,谱系确定的遗传基础仍未得到解决。最近,已经建立了一些体外试验,这些试验支持从多能细胞发育为定向B细胞祖细胞。这些试验提供了一个新的系统,在这个系统中可以追踪和操纵B谱系定向过程。在这篇综述中,我们提出了一个从多能祖细胞到定向B细胞祖细胞的B谱系进展模型,并讨论了定向过程的潜在介导因子。

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