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人类胎儿造血及淋巴细胞培养中调节性T淋巴细胞表型的表达

Expression of regulatory T-lymphocyte phenotype in human fetal hemopoietic and lymphoid cell culture.

作者信息

Sharova N I, Donetskova A D, Dubrovina I V, Sukhikh G T, Yarilin A A

机构信息

Institute of Immunology, FMBA.

出版信息

Bull Exp Biol Med. 2006 Apr;141(4):524-9. doi: 10.1007/s10517-006-0213-1.

Abstract

Cells with regulatory T-cell phenotype (Treg, CD4+CD25(hi)) were not detected in human fetal thymus, liver, bone marrow, spleen, and among blood mononuclears of 14-28-week gestation. The cells of the majority of these fetal thymuses express Treg specific marker (FOXP3 transcription marker) gene. Culturing of fetal liver and bone marrow cells on a monolayer of thymic epithelial cells induced expression of FOXP3 gene, but induction of CD4+CD25+ membrane phenotype was detected in only 1 of 8 studied cultures (in liver and bone marrow cells). Induction of Treg differentiation is to a greater extent determined by the characteristics of hemopoietic organ cells than of thymic epithelial cells.

摘要

在人胎儿胸腺、肝脏、骨髓、脾脏以及妊娠14 - 28周的血液单核细胞中未检测到具有调节性T细胞表型(Treg,CD4 + CD25(hi))的细胞。这些胎儿胸腺中的大多数细胞表达Treg特异性标志物(FOXP3转录标志物)基因。将胎儿肝脏和骨髓细胞培养在胸腺上皮细胞单层上可诱导FOXP3基因表达,但在8个研究培养物中仅有1个(在肝脏和骨髓细胞中)检测到CD4 + CD25 +膜表型的诱导。调节性T细胞分化的诱导在更大程度上取决于造血器官细胞的特性,而非胸腺上皮细胞的特性。

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