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造血干细胞最早谱系定向步骤的描绘:新进展、争议与重大挑战

Delineation of the earliest lineage commitment steps of haematopoietic stem cells: new developments, controversies and major challenges.

作者信息

Buza-Vidas Natalija, Luc Sidinh, Jacobsen Sten Eirik W

机构信息

Haematopoietic Stem Cell Laboratory, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Headington, Oxford, UK.

出版信息

Curr Opin Hematol. 2007 Jul;14(4):315-21. doi: 10.1097/MOH.0b013e3281de72bb.

DOI:10.1097/MOH.0b013e3281de72bb
PMID:17534155
Abstract

PURPOSE OF REVIEW

This review addresses recently reported evidence for alternative cellular pathways for haematopoietic stem cell lineage commitment.

RECENT FINDINGS

Using various approaches, several laboratories suggested the existence of adult as well as foetal multipotent progenitor cells with combined B cell, T cell and granulocyte/macrophage potential, but little or no megakaryocyte/erythroid potential. Compared with haematopoietic stem cells, these multipotent progenitor cells exhibited downregulated transcriptional expression of genes of the megakaryocyte/erythroid lineages and upregulated expression of lymphoid lineage genes. The existence of these lineage-restricted multipotent progenitor cells suggests that the first lineage commitment step of haematopoietic stem cells does not result in strict separation into myelopoiesis and lymphopoiesis, and that there might be alternative pathways for commitment toward different lineage fates. These findings have been questioned by other studies, however. To resolve this controversy and establish the complete road map for haematopoietic lineage commitment, improved tools and more stringent standards for how to identify and characterize lineage fate options of distinct stem and progenitor cells are needed.

SUMMARY

Current and future progress in establishing the complete cellular roadmap for haematopoietic lineage commitment will permit identification and characterization of key regulators of lineage fate decisions in haematopoietic stem cells.

摘要

综述目的

本综述探讨了近期报道的造血干细胞谱系定向分化的替代细胞途径的证据。

最新发现

通过各种方法,多个实验室提出存在具有B细胞、T细胞和粒细胞/巨噬细胞潜能,但几乎没有或没有巨核细胞/红细胞潜能的成年及胎儿多能祖细胞。与造血干细胞相比,这些多能祖细胞巨核细胞/红细胞谱系基因的转录表达下调,而淋巴细胞谱系基因的表达上调。这些谱系受限的多能祖细胞的存在表明,造血干细胞的首个谱系定向分化步骤并不会导致严格分离为髓系造血和淋巴系造血,并且可能存在通向不同谱系命运的替代途径。然而,其他研究对这些发现提出了质疑。为了解决这一争议并建立造血谱系定向分化的完整路线图,需要改进工具以及更严格的标准来识别和表征不同干细胞和祖细胞的谱系命运选择。

总结

在建立造血谱系定向分化的完整细胞路线图方面,当前和未来的进展将有助于识别和表征造血干细胞谱系命运决定的关键调节因子。

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