Regulation of IL-2 beta receptor expression and beta-chain mRNA by human thymocytes.
Regulation of IL-2 beta receptor expression and beta-chain mRNA by human thymocytes.
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人类胸腺细胞对 IL-2 β 受体表达和 β 链 mRNA 的调节。
DOI:
10.1111/j.1365-2249.1992.tb06429.x
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发表时间:
1992
影响因子:
4.6
通讯作者:
Marcelli,A
中科院分区:
文献类型:
--
作者:
Reem,GH;Han,X;Marcelli,A
The high affinity form of the human IL-2 receptor (IL-2R) has two known components, the IL-2Rα (p55) and the IL-2Rβ chain (p75). We have previously shown that recombinant IL-2 (rIL-2) could induce the expression of the α-chain (p55) on T cells and thymocytes, and increase this expression following suboptimal activation with concanavalin A (Con A) in combination with IL-2. An increase in the accumulation of IL-2Rα-specific mRNA induced by rIL-2 in T cells and thymocytes had also been documented. We report here that the expression of IL-2Rβ on the cell surface can be demonstrated on human thymocytes by the binding of Mik β1, a MoAb directed against an epitope of the β-chain. The IL-2Rβ chain is constitutively expressed on freshly isolated thymocytes; this expression can be increased in thymocytes activated with Con A in combination with IL-2 or tetradecanoylphorbol 13-acetaie (TPA). Blocking the formation of high affinity receptors with a MoAb directed against the α-chain of the receptor results in an increase in the display of IL-2Rβ as evidenced by binding of MoAb Mik β1. The accumulation of IL-2Rβ specific mRNA is observed in freshly isolated thymocytes and it is increased in thymocytes cultured with rIL-2 alone, with Con A. and further enhanced by the addition of rIL-2 in combination with Con A or with TPA. Cyclosporine (CsA), which inhibits the accumulation of lymphokine-specific mRNA of thymocytes, does not inhibit the induction of the accumulation orIL-2Rβ-specific mRNA. This is analogous to its effect on the expression of the α-chain (p55), and the accumulation of α-chain-specific mRNA.