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干细胞因子与c-Kit之间的相互作用是肠道免疫系统稳态所必需的。

Interactions between stem cell factor and c-Kit are required for intestinal immune system homeostasis.

作者信息

Puddington L, Olson S, Lefrançois L

机构信息

Department of Medicine, University of Connecticut Health Center, Farmington 06030.

出版信息

Immunity. 1994 Dec;1(9):733-9. doi: 10.1016/s1074-7613(94)80015-4.

Abstract

Interactions between stem cell factor (SCF) and its receptor, c-Kit, are important for development of hematopoietic, melanocytes, and germ cells. T lymphocytes appeared normal in c-Kit (W/Wv) or SCF (SI/SId) mutant mice, except for those residing within the intestinal epithelium, the intraepithelial lymphocytes (IEL). Normally, IEL are composed of equal numbers of cells with alpha beta or gamma delta T cell receptors. In mutant mice, beginning at 6-8 weeks of age, the number of gamma delta IEL decreased, whereas alpha beta IEL increased. The latter was due largely to an increased CD4+ CD8+ TCR alpha beta subset, suggesting that these cells may be intermediates in the alpha beta IEL lineage. c-Kit or SCF was expressed by IEL or intestinal epithelial cells, respectively, indicating a potential for direct intercellular interaction. This possibility was supported by reconstitution studies that demonstrated that c-Kit mutations directly affected IEL. Thus, SCF-c-Kit interactions are important for homeostasis of the intestinal immune compartment.

摘要

干细胞因子(SCF)与其受体c-Kit之间的相互作用对于造血细胞、黑素细胞和生殖细胞的发育至关重要。在c-Kit(W/Wv)或SCF(SI/SId)突变小鼠中,T淋巴细胞看起来正常,但位于肠上皮内的上皮内淋巴细胞(IEL)除外。正常情况下,IEL由数量相等的具有αβ或γδ T细胞受体的细胞组成。在突变小鼠中,从6至8周龄开始,γδ IEL的数量减少,而αβ IEL增加。后者主要是由于CD4+ CD8+ TCR αβ亚群增加,这表明这些细胞可能是αβ IEL谱系中的中间细胞。IEL或肠上皮细胞分别表达c-Kit或SCF,表明存在直接细胞间相互作用的可能性。重建研究支持了这一可能性,该研究表明c-Kit突变直接影响IEL。因此,SCF-c-Kit相互作用对于肠道免疫区室的稳态很重要。

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