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在自然杀伤细胞与B细胞和T细胞生成过程中转录因子PU.1的差异需求。

Differential requirement for the transcription factor PU.1 in the generation of natural killer cells versus B and T cells.

作者信息

Colucci F, Samson S I, DeKoter R P, Lantz O, Singh H, Di Santo J P

机构信息

Laboratory for Cytokines and Lymphoid Development, Pasteur Institute, Paris, France.

出版信息

Blood. 2001 May 1;97(9):2625-32. doi: 10.1182/blood.v97.9.2625.

Abstract

PU.1 is a member of the Ets family of transcription factors required for the development of various lymphoid and myeloid cell lineages, but its role in natural killer (NK) cell development is not known. The study shows that PU.1 is expressed in NK cells and that, on cell transfer into alymphoid Rag2/gammac(-/-) mice, hematopoietic progenitors of PU.1(-/-) fetal liver cells could generate functional NK cells but not B or T cells. Nevertheless, the numbers of bone marrow NK cell precursors and splenic mature NK cells were reduced compared to controls. Moreover, PU.1(-/-) NK cells displayed reduced expression of the receptors for stem cell factor and interleukin (IL)-7, suggesting a nonredundant role for PU.1 in regulating the expression of these cytokine receptor genes during NK cell development. PU.1(-/-) NK cells also showed defective expression of inhibitory and activating members of the Ly49 family and failed to proliferate in response to IL-2 and IL-12. Thus, despite the less stringent requirement for PU.1 in NK cell development compared to B and T cells, PU.1 regulates NK cell differentiation and homeostasis.

摘要

PU.1是Ets转录因子家族的成员,是多种淋巴样和髓样细胞谱系发育所必需的,但它在自然杀伤(NK)细胞发育中的作用尚不清楚。该研究表明,PU.1在NK细胞中表达,并且在将细胞转移到无淋巴细胞的Rag2/γc(-/-)小鼠中时,PU.1(-/-)胎肝细胞的造血祖细胞可以产生功能性NK细胞,但不能产生B细胞或T细胞。然而,与对照组相比,骨髓NK细胞前体和脾脏成熟NK细胞的数量减少。此外,PU.1(-/-)NK细胞显示干细胞因子和白细胞介素(IL)-7受体的表达降低,这表明PU.1在NK细胞发育过程中调节这些细胞因子受体基因的表达方面具有非冗余作用。PU.1(-/-)NK细胞还显示Ly49家族抑制性和激活性成员的表达缺陷,并且不能响应IL-2和IL-12而增殖。因此,尽管与B细胞和T细胞相比,NK细胞发育对PU.1的要求不那么严格,但PU.1调节NK细胞的分化和稳态。

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