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人B淋巴细胞上膜Ia的调节

The modulation of membrane Ia on human B lymphocytes.

作者信息

Kehrl J H, Muraguchi A, Fauci A S

出版信息

Cell Immunol. 1985 May;92(2):391-403. doi: 10.1016/0008-8749(85)90020-6.

Abstract

Using flow cytometry techniques, changes in surface Ia (DR and DS) expression on human B lymphocytes were correlated with changes in the cell cycle following stimulation with anti-mu. The effect of interleukin (IL)-1, IL-2, B-cell growth factor (BCGF), and interferons on Ia expression on resting B cells was also examined. A population of resting B lymphocytes was cultured in vitro with 100 micrograms/ml of anti-mu and immunofluorescently stained for DR and DS at various times following stimulation. Detectable increases in DR and DS expression were found within 8 hr, and the major increases (twofold and fourfold) in DR and DS expression occurred over the next 48 hr. Using cell cycle inhibitors and propidium iodide staining, it was demonstrated that the enhanced DR and DS expression following anti-mu stimulation began during G0 to G1 transition and increased as the cells progressed through G1 phase. During S and G2/M phases, there were minimal further increases in surface Ia. Although prolonged exposure of B cells to anti-mu was required for cellular activation, cell size enlargement, and progression into S phase, a brief exposure to anti-mu, insufficient for cellular activation, markedly enhanced Ia expression. Thus anti-mu-stimulated resting human B lymphocytes rapidly increase their surface Ia expression. This increase occurs predominantly prior to entrance into S phase and can occur in the absence of significant cellular activation. Interferons have been reported to modulate surface Ia expression on a human lymphoid cell line and on monocytes and supernatants with BCGF activity to enhance surface Ia expression on murine B cells; however, neither alpha-interferon, gamma-interferon, IL-1, IL-2, nor BCGF modified surface DR expression on normal resting human B cells.

摘要

运用流式细胞术,研究了抗μ刺激后人B淋巴细胞表面Ia(DR和DS)表达的变化与细胞周期变化之间的相关性。还检测了白细胞介素(IL)-1、IL-2、B细胞生长因子(BCGF)和干扰素对静息B细胞Ia表达的影响。将一群静息B淋巴细胞在体外与100微克/毫升的抗μ一起培养,并在刺激后的不同时间用免疫荧光法对DR和DS进行染色。在8小时内可检测到DR和DS表达增加,在接下来的48小时内DR和DS表达出现主要增加(两倍和四倍)。使用细胞周期抑制剂和碘化丙啶染色,证明抗μ刺激后DR和DS表达增强始于G0到G1期转变,并随着细胞进入G1期而增加。在S期和G2/M期,表面Ia进一步增加极少。尽管B细胞需要长时间暴露于抗μ才能发生细胞活化、细胞大小增大并进入S期,但短暂暴露于抗μ(不足以引起细胞活化)可显著增强Ia表达。因此,抗μ刺激的静息人B淋巴细胞迅速增加其表面Ia表达。这种增加主要发生在进入S期之前,且可在无明显细胞活化的情况下发生。据报道,干扰素可调节人淋巴细胞系、单核细胞以及具有BCGF活性的上清液中表面Ia的表达,从而增强鼠B细胞表面Ia的表达;然而,α干扰素、γ干扰素、IL-1、IL-2或BCGF均未改变正常静息人B细胞表面DR的表达。

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