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细胞培养中正常和转化的3T3成纤维细胞产生前列腺素的情况。

Prostaglandin production by normal and transformed 3T3 fibroblasts in cell culture.

作者信息

Hammarström S

出版信息

Eur J Biochem. 1977 Mar 15;74(1):7-12. doi: 10.1111/j.1432-1033.1977.tb11360.x.

Abstract

Prostaglandin E2 and prostaglandin F2alpha were quantitatively determined in culture media from Balb/c 3T3 fibroblasts and two virus-transformed derivatives of these cells. Regular and (simian virus 40)-transformed 3T3 cells produced low and almost identical prostaglandin E2 concentrations. The levels were maximal (10 ng/ml) 24 h after planting and decreased during the next 96 h to 2.5 ng/ml. In contrast, polyoma-virus-transformed 3T3 cells produced prostaglandin E2 continuously for 120 h, giving a final concentration of 270 ng/ml. Fresh medium supplemented with calf serum reinitiated prostaglandin production in confluent 3T3 cells. Maximal prostaglandin E2 concentrations were obtained between 6 and 18 h after medium change and were proportional to the serum concentration of the medium. Indomethacin (10(-6) M) completely inhibited prostaglandin E2 production but not prostaglandin F2alpha production by these cells.

摘要

在来自Balb/c 3T3成纤维细胞及其两种病毒转化衍生物的培养基中,对前列腺素E2和前列腺素F2α进行了定量测定。正常的和(猴病毒40)转化的3T3细胞产生的前列腺素E2浓度较低且几乎相同。接种后24小时,其水平达到最大值(10 ng/ml),并在接下来的96小时内降至2.5 ng/ml。相比之下,多瘤病毒转化的3T3细胞连续120小时产生前列腺素E2,最终浓度为270 ng/ml。补充有小牛血清的新鲜培养基可重新启动汇合的3T3细胞中的前列腺素生成。换液后6至18小时可获得最大前列腺素E2浓度,且与培养基中的血清浓度成正比。吲哚美辛(10^(-6) M)可完全抑制这些细胞产生前列腺素E2,但不抑制前列腺素F2α的产生。

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