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对氨基苯甲酸 N-木糖苷钠盐(K-247)对正常淋巴细胞和白血病细胞代谢及功能的影响。

Effect of p-aminobenzoic acid N-xyloside sodium salt (K-247) on metabolism and functions of normal lymphocytes and leukemic cells.

作者信息

Toyoshima S, Nakajima S, Oguchi Y, Osawa T

出版信息

J Pharmacobiodyn. 1982 Jun;5(6):430-8. doi: 10.1248/bpb1978.5.430.

Abstract

An N-xyloside derivative of p-aminobenzoic acid, K-247, was investigated for the ability to induce changes of Phospholipid metabolism and membrane transport in murine splenic lymphocytes and leukemic cells. K-247 induced an increase of [3H] methyl group incorporation into phospholipid in both normal lymphocytes and leukemic cells (L-1210 and M1 cells). However, K-247 accelerated the turnover of phosphatidylinositol (PI) measured by [32P] incorporation into PI in L-1210 cells and Ml cells but not in normal lymphocytes. 45Ca2+ influx into normal lymphocytes and leukemic cells was also increased by K-247. A methyltransferase inhibitor, 5'-deoxy-5'-S-isobutyl adenosine (SIBA), suppressed both the increase of phospholipid methylation and that of Ca2+ influx. It seemed that Ca2+ transport might be regulated by membrane phospholipid methylation. On the other hand, K-247 was found to suppress [3H] aminoisobutylic acid (AIB) uptake into L-1210 cells and Ml cells. Protein synthesis in L-1210 cells and Ml cells slightly decreased but RNA and DNA syntheses in both normal and leukemic cells were not affected by K-247. These results suggest that K-247 mainly acts on cell membranes, which are more sensitive to K-247 in leukemic cells than in normal lymphocytes. K-247 also induced differentiation of Ml cells into macrophages and granulocytes with phagocytic activity and morphological characteristics. Moreover, K-247 elevated the Con A response of murine thymocytes, most of which were immature T cells and had low reactivity to Con A, and caused a decrease of Thy 1.2 antigen on thymocytes. It seemed that K-247 also affected maturation of thymocytes.

摘要

对对氨基苯甲酸的N-木糖苷衍生物K-247诱导小鼠脾淋巴细胞和白血病细胞磷脂代谢和膜转运变化的能力进行了研究。K-247诱导正常淋巴细胞和白血病细胞(L-1210和M1细胞)中[3H]甲基掺入磷脂的量增加。然而,K-247加速了通过[32P]掺入L-1210细胞和M1细胞中的磷脂酰肌醇(PI)的周转,但在正常淋巴细胞中未观察到这种现象。K-247还增加了45Ca2+流入正常淋巴细胞和白血病细胞。甲基转移酶抑制剂5'-脱氧-5'-S-异丁基腺苷(SIBA)抑制了磷脂甲基化的增加和Ca2+流入的增加。似乎Ca2+转运可能受膜磷脂甲基化的调节。另一方面,发现K-247抑制[3H]氨基异丁酸(AIB)摄取到L-1210细胞和M1细胞中。L-1210细胞和M1细胞中的蛋白质合成略有下降,但正常和白血病细胞中的RNA和DNA合成均不受K-247影响。这些结果表明,K-247主要作用于细胞膜,白血病细胞的细胞膜对K-247比正常淋巴细胞更敏感。K-247还诱导M1细胞分化为具有吞噬活性和形态特征的巨噬细胞和粒细胞。此外,K-247提高了小鼠胸腺细胞的刀豆蛋白A反应,其中大多数是未成熟的T细胞,对刀豆蛋白A的反应性较低,并导致胸腺细胞上Thy 1.2抗原减少。似乎K-247也影响胸腺细胞的成熟。

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