血浆纤维连接蛋白对大鼠淋巴细胞转化的调节作用。

D B Lause, J E Doran, J A Houston, D H Beezhold
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引用次数: 0

摘要

研究纯化大鼠血浆纤维连接蛋白(Fn)影响非特异性淋巴细胞向各种有丝分裂原转化的能力。Fn添加到淋巴结细胞(LNC),通过植物血凝素(PHA),豆豆蛋白A (Con A),或细菌脂多糖(LPS)刺激,导致非细胞毒性的剂量依赖性抑制胚源反应。Fn浓度为10-50微克/培养时,LNC对PHA和LPS的反应有效抑制(大于50%)。Fn的存在对Con A的增殖反应影响较小:仅在最高浓度的Fn研究中观察到50%的抑制作用。在抑制淋巴细胞对PHA的反应方面,低浓度的Fn比贫Fn更有效。Fn调节活性的最佳表达发生在PHA和LPS反应的增殖高峰期间和之后。为了引起最大的抑制作用,有必要在有丝分裂原刺激LNC后12小时内存在Fn。抑制似乎不是fn -有丝分裂原复合物减少可用于刺激的有丝分裂原数量的结果,因为PHA或LPS浓度的增加都没有显著降低抑制作用。此外,抑制作用不受培养基中存在的胎牛血清浓度的影响。因此,Fn可能在炎症部位和组织修复区域发挥重要的非特异性免疫调节因子的作用。
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Modulation of rat lymphocyte transformation by plasma fibronectin.

Purified rat plasma fibronectin (Fn) was studied for its ability to influence nonspecific lymphocyte transformation to various mitogens. Fn added to lymph node cells (LNC) stimulated with phytohemagglutinin (PHA), concanavalin A (Con A), or bacterial lipopolysaccharide (LPS) resulted in a noncytotoxic dose-dependent inhibition of the blastogenic response. Effective inhibition (greater than 50%) of LNC responses to PHA and LPS occurred with concentrations of Fn that ranged from 10-50 micrograms/culture. The proliferative response to Con A was less affected by the presence of Fn: 50% inhibition was observed only with the highest concentration of Fn studied. Fn at low concentrations was more effective than Fn-depleted plasma in inhibiting lymphocyte responses to PHA. Optimal expression of the regulatory activity of Fn occurs during and following the peak proliferative period for both PHA and LPS responses. In order to evoke maximum inhibition it is necessary for Fn to be present within 12 hours following stimulation of LNC with mitogen. Inhibition does not appear to be the result of Fn-mitogen complexes which reduce the amount of mitogen available for stimulation, since increasing concentrations of either PHA or LPS did not significantly reduce the inhibitory effect. Furthermore, inhibition was not influenced by the concentration of fetal calf serum present in the culture medium. Thus, Fn may function as an important nonspecific immunoregulatory factor at inflammatory sites and in areas of tissue repair.

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