Damle R N, Gangal S G, Advani S H
Immunology Division, Cancer Research Institute, Tata Memorial Centre, Bombay.
Indian J Med Res. 1992 Aug;96:230-5.
T cell activation process in patients of Hodgkin's disease was studied in terms of cellular protein phosphorylation following interaction of T lymphocytes with mitogen PHA. Peripheral blood lymphocytes from Hodgkin's disease patients and healthy donors, labelled with [32P] were activated with PHA. The cell lysates were subjected to SDS-PAGE, 2-dimensional gel analysis and were autoradiographed. It was observed that lymphocytes from both Hodgkin's disease patients and healthy donors followed similar time kinetics of phosphorylation. Nine of the eleven major protein bands, resolved on SDS-PAGE in the molecular weight range of 15.7-98 kD showed reduced phosphorylation (ratios of densitometric readings taken after and before stimulation) compared to that of healthy donors. Isoelectric focusing of these major protein bands in 2-dimensional gels further resolved them into about 27 proteins. Most of these showed increased phosphorylation in lysates of activated lymphocytes from healthy donors compared to that of Hodgkin's disease patients. The results showed a defect even at an early stage in terms of inadequate cellular protein phosphorylation.
通过T淋巴细胞与促有丝分裂原PHA相互作用后细胞蛋白磷酸化情况,对霍奇金病患者的T细胞激活过程进行了研究。用[32P]标记的霍奇金病患者和健康供体的外周血淋巴细胞,用PHA激活。细胞裂解物进行SDS-PAGE、二维凝胶分析并进行放射自显影。观察到霍奇金病患者和健康供体的淋巴细胞遵循相似的磷酸化时间动力学。在SDS-PAGE上分辨出的分子量范围为15.7 - 98 kD的11条主要蛋白带中,有9条与健康供体相比显示磷酸化减少(刺激前后光密度读数的比值)。这些主要蛋白带在二维凝胶中的等电聚焦进一步将它们解析为约27种蛋白质。与霍奇金病患者相比,这些蛋白质中的大多数在健康供体活化淋巴细胞的裂解物中显示磷酸化增加。结果表明,即使在早期阶段,细胞蛋白磷酸化不足也存在缺陷。