Singh M, Notterman D A, Metakis L
Department of Pediatrics, New York Hospital-Cornell Medical Center, NY 10021.
Circ Shock. 1993 Apr;39(4):275-8.
The effect of tumor necrosis factor alpha (TNF alpha) on lymphocyte beta 2-adrenergic receptor response is reported. Isoproterenol-mediated cyclic-3,5-adenosine monophosphate (cAMP) production by intact lymphocytes preincubated with isotonic buffer or TNF alpha was studied. TNF alpha at 1 ng/ml and 100 ng/ml reduced isoproterenol-stimulated cAMP generation by 15% and 27% over the respective basal values. Stimulation of lymphocytes with forskolin or prostaglandin E1 was minimally affected, indicating that the effect of TNF alpha was due neither to nonspecific toxicity nor to its influence on the nucleotide regulatory protein complex or the catalytic adenylate cyclase component of the beta 2-adrenergic receptor complex system. Rather, TNF alpha appeared to affect the receptor recognition unit specifically. TNF alpha causes homologous desensitization of lymphocyte beta 2-adrenergic receptor response.
据报道,肿瘤坏死因子α(TNFα)对淋巴细胞β2 - 肾上腺素能受体反应有影响。研究了用等渗缓冲液或TNFα预孵育的完整淋巴细胞中异丙肾上腺素介导的环3,5 - 腺苷单磷酸(cAMP)生成情况。1 ng/ml和100 ng/ml的TNFα使异丙肾上腺素刺激的cAMP生成量分别比各自的基础值降低了15%和27%。用福斯高林或前列腺素E1刺激淋巴细胞受到的影响最小,这表明TNFα的作用既不是由于非特异性毒性,也不是由于其对β2 - 肾上腺素能受体复合系统的核苷酸调节蛋白复合物或催化腺苷酸环化酶成分的影响。相反,TNFα似乎特异性地影响受体识别单位。TNFα导致淋巴细胞β2 - 肾上腺素能受体反应的同源脱敏。