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在37摄氏度预孵育的猫淋巴细胞自发红细胞花环形成增加。

Increased spontaneous erythrocyte rosette formation of feline lymphocytes preincubated at 37 degrees C.

作者信息

Cockerell G L, Baldwin C L

出版信息

J Immunol Methods. 1979;28(3-4):369-79. doi: 10.1016/0022-1759(79)90202-3.

Abstract

Preincubation of feline peripheral blood lymphocytes (PBL) in complete medium at 37 degrees C for up to 24 h resulted in as much as a 5.5-fold increase in the per cent of T cells detectable by spontaneous E rosette formation with guinea pig erythrocytes, as compared to non-preincubated PBL. Under these same conditions, the percent of B cells, detected by EAC rosette formation, remained unchanged. Preincubation with either thymosin or levamisole caused no increase in E rosettes other than that seen with complete medium alone. The preincubation-associated increase in E rosettes was temperature dependent, independent of the source of serum in the preincubation medium, not influenced by the lymphocyte isolation procedure, and not observed when feline thymocytes were tested in place of PBL. No increase in functional activity, assayed by phytomitogen-induced lymphocyte blastogenesis, was observed in preincubated as compared to non-preincubated PBL. These results suggested either a non-specific unmasking, or the differentiation and acquisition, of E receptors by feline PBL during the preincubation procedure.

摘要

猫外周血淋巴细胞(PBL)在完全培养基中于37℃预孵育长达24小时,与未预孵育的PBL相比,通过与豚鼠红细胞自发形成E花环检测到的T细胞百分比增加了5.5倍。在相同条件下,通过EAC花环形成检测到的B细胞百分比保持不变。用胸腺素或左旋咪唑预孵育除了单独使用完全培养基时观察到的情况外,不会导致E花环增加。预孵育相关的E花环增加与温度有关,与预孵育培养基中的血清来源无关,不受淋巴细胞分离程序的影响,并且当用猫胸腺细胞代替PBL进行测试时未观察到。与未预孵育的PBL相比,在预孵育的PBL中未观察到通过植物血凝素诱导的淋巴细胞增殖检测到的功能活性增加。这些结果表明,在预孵育过程中,猫PBL对E受体进行了非特异性的暴露,或者进行了分化和获得。

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