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细胞因子对体外培养的外周血单个核细胞β2 -肾上腺素能受体密度的影响。

Influence of cytokines on the density of beta 2-adrenergic receptors on peripheral blood mononuclear cells in vitro.

作者信息

Krause A, Steitz A, von Wichert P, Baerwald C

机构信息

Department of Internal Medicine, Philipps-University, Marburg/Lahn.

出版信息

Cytokine. 1995 Apr;7(3):273-6. doi: 10.1006/cyto.1995.0032.

Abstract

Previous investigations have demonstrated a decrease of the number of beta 2-adrenergic receptors (beta 2R) on peripheral blood mononuclear cells (PBMC) in patients with rheumatic diseases that correlated with the systemic inflammatory activity. However, the main factor(s) modulating the beta 2R on lymphocytes in inflammatory diseases are still unidentified. The present study aimed at evaluating the influence of interleukin 1 beta (IL-1 beta) and interleukin 2 (IL-2) on the number and on the dissociation constant (KD) of beta 2R on PBMC in vitro. PBMC from healthy volunteers were incubated with different concentrations of IL-1 beta (10-100 U/ml) or IL-2 (10-50 U/ml) for 1,6,12,24 and 72 hours (h), respectively. Cultures with medium alone served as controls. beta 2R were determined using a radioligand binding assay with 125Iodo-cyanopindolol. The results showed a significant spontaneous decline of beta 2R after 72 h (mean +/- SEM = 2674 +/- 392 binding sites/cell (bs/c) vs. 1131 +/- 149 bs/c P < 0.02). IL-2 at a concentration of 50 U/ml diminished this spontaneous reduction of beta 2R numbers significantly (control: 1439 +/- 139 bs/c vs. IL-2: 1724 +/- 107 bs/c, P < 0.05). However, beta 2R densities did not hold baseline levels and were still significantly lower as compared to preculture values. Incubation with 100 U/ml IL-1 beta for 6 h induced a significant increase of beta 2R densities (control: 1760 +/- 214 bs/c vs. IL-1: 2233 +/- 424 bs/c, P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

先前的研究表明,风湿性疾病患者外周血单核细胞(PBMC)上的β2 - 肾上腺素能受体(β2R)数量减少,且这与全身炎症活动相关。然而,炎症性疾病中调节淋巴细胞上β2R的主要因素仍未明确。本研究旨在评估白细胞介素1β(IL - 1β)和白细胞介素2(IL - 2)对体外PBMC上β2R数量和解离常数(KD)的影响。分别将来自健康志愿者的PBMC与不同浓度的IL - 1β(10 - 100 U/ml)或IL - 2(10 - 50 U/ml)孵育1、6、12、24和72小时(h)。仅含培养基的培养物作为对照。使用125I - 氰基吲哚洛尔放射性配体结合测定法测定β2R。结果显示,72小时后β2R出现显著的自发下降(平均值±标准误 = 2674±392个结合位点/细胞(bs/c)对1131±149 bs/c,P < 0.02)。浓度为50 U/ml的IL - 2显著减少了β2R数量的这种自发减少(对照:1439±139 bs/c对IL - 2:1724±107 bs/c,P < 0.05)。然而,β2R密度未保持在基线水平,与培养前值相比仍显著较低。用100 U/ml IL - 1β孵育6小时导致β2R密度显著增加(对照:1760±214 bs/c对IL - 1:2233±424 bs/c,P < 0.05)。(摘要截断于250字)

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