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在高浓度、无丝裂原性的伴刀豆球蛋白A作用下,小淋巴细胞中早期酶产生的激活。

Activation of early enzyme production in small lymphocytes in response to high, nonmitogenic concentrations of concanavalin A.

作者信息

Degen J L, Morris D R

出版信息

Proc Natl Acad Sci U S A. 1980 Jun;77(6):3479-83. doi: 10.1073/pnas.77.6.3479.

Abstract

Lymphocyte mitogenesis is generally assessed by measuring the incorporation of [(3)H]thymidine into DNA. By this criterion, small lymphocytes, which are activated by relatively low doses of concanavalin A, are either unresponsive to or inhibited by higher concentrations. Because lymphocytes begin to synthesize DNA about 24 hr after addition of mitogen, the response is far removed temporally from the initial stimulus. We have chosen to use the induction of S-adenosylmethionine decarboxylase (S-adenosyl-L-methionine carboxy-lyase, EC 4.1.1.50) to assess early activation events in bovine lymphocytes. Adenosylmethionine decarboxylase induction is bimodal, with an initial phase beginning 3 hr after addition of concanavalin A and a second wave coinciding with the onset of DNA synthesis. The initial accumulation of the decarboxylase (0-9 hr) in cultures treated with "nonmitogenic" levels of concanavalin A (108 mug/ml) was similar to that observed in cultures stimulated with optimally mitogenic doses (18 mug/ml). The early induction of ornithine decarboxylase (L-ornithine carboxy-lyase, EC 4.1.1.17) was also similar under these two culture conditions. However, the second phase of adenosylmethionine decarboxylase accumulation, the induction of thymidine kinase (ATP: thymidine 5'-phosphotransferase, EC 2.7.1.21), and DNA replication were blocked at the higher concentrations of concanavalin A. The inhibition of late events by high doses of concanavalin A was reversible. Cells treated with alpha-methyl-D-mannopyranoside 25 hr after addition of a high dose of lectin responded with a second period of adenosylmethionine decarboxylase accumulation, induction of thymidine kinase, and progression through S phase. These results suggest that initial lymphocyte activation occurs normally at high doses of concanavalin A, but that the cells are reversibly blocked prior to induction of "late" enzymes and progression through S phase.

摘要

淋巴细胞有丝分裂通常通过测量[³H]胸苷掺入DNA的情况来评估。根据这一标准,被相对低剂量的刀豆球蛋白A激活的小淋巴细胞,对更高浓度的刀豆球蛋白A无反应或受到抑制。由于淋巴细胞在添加促有丝分裂原后约24小时开始合成DNA,所以该反应在时间上与初始刺激相距甚远。我们选择使用S -腺苷甲硫氨酸脱羧酶(S -腺苷-L -甲硫氨酸羧基裂解酶,EC 4.1.1.50)的诱导来评估牛淋巴细胞中的早期激活事件。腺苷甲硫氨酸脱羧酶的诱导是双峰的,在添加刀豆球蛋白A后3小时开始有一个初始阶段,第二波与DNA合成的开始相吻合。在用“非促有丝分裂”水平的刀豆球蛋白A(108微克/毫升)处理的培养物中,脱羧酶的初始积累(0 - 9小时)与用最佳促有丝分裂剂量(18微克/毫升)刺激的培养物中观察到的相似。在这两种培养条件下,鸟氨酸脱羧酶(L -鸟氨酸羧基裂解酶,EC 4.1.1.17)的早期诱导也相似。然而,在较高浓度的刀豆球蛋白A下,腺苷甲硫氨酸脱羧酶积累的第二阶段、胸苷激酶(ATP:胸苷5'-磷酸转移酶,EC 2.7.1.21)的诱导以及DNA复制被阻断。高剂量刀豆球蛋白A对后期事件的抑制是可逆的。在添加高剂量凝集素25小时后用α-甲基-D-甘露吡喃糖苷处理的细胞,会出现腺苷甲硫氨酸脱羧酶积累、胸苷激酶诱导以及通过S期进展的第二个阶段。这些结果表明,在高剂量刀豆球蛋白A作用下,淋巴细胞的初始激活正常发生,但细胞在诱导“晚期”酶和通过S期进展之前被可逆性阻断。

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