Expression of steroidogenic enzymes and metabolism of steroids in COS-7 cells known as non-steroidogenic cells.
Expression of steroidogenic enzymes and metabolism of steroids in COS-7 cells known as non-steroidogenic cells.
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DOI:
10.1038/s41598-018-20226-2
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发表时间:
2018-02-01
影响因子:
4.6
通讯作者:
Tsutsui K
中科院分区:
文献类型:
--
作者:
Nozaki M;Haraguchi S;Miyazaki T;Shigeta D;Kano N;Lei XF;Kim-Kaneyama JR;Minakata H;Miyazaki A;Tsutsui K
The COS-7 (CV-1 in Origin with SV40 genes) cells are known as non-steroidogenic cells because they are derived from kidney cells and the kidney is defined as a non-steroidogenic organ. Therefore, COS-7 cells are used for transfection experiments to analyze the actions of functional molecules including steroids. However, a preliminary study suggested that COS-7 cells metabolize [3H]testosterone to [3H]androstenedione. These results suggest that COS-7 cells are able to metabolize steroids. Therefore, the present study investigated the expression of steroidogenic enzymes and the metabolism of steroids in COS-7 cells. RT-PCR analyses demonstrated the expressions of several kinds of steroidogenic enzymes, such as cytochrome P450 side-chain cleavage enzyme, 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase, cytochrome P450 7α-hydroxylase, cytochrome P450 17α-hydroxylase/17,20-lyase, 17β-hydroxysteroid dehydrogenase, 5α-reductase, cytochrome P450 21-hydroxylase, cytochrome P450 11β-hydroxylase, and cytochrome P450 aromatase in COS-7 cells. In addition, steroidogenic enzymes 3β-HSD, P4507α, 5α-reductase, P450c17, P450c21, P450c11β, and 17β-HSD actively metabolized various steroids in cultured COS-7 cells. Finally, we demonstrated that 17β-HSD activity toward androstenedione formation was greater than other steroidogenic enzyme activities. Our results provide new evidence that COS-7 cells express a series of steroidogenic enzyme mRNAs and actively metabolize a variety of steroids.
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影响因子:
4.6
作者:
Haraguchi S;Yamamoto Y;Suzuki Y;Hyung Chang J;Koyama T;Sato M;Mita M;Ueda H;Tsutsui K
通讯作者:
Tsutsui K
影响因子:
64.5
作者:
SMALE, ST;BALTIMORE, D
通讯作者:
BALTIMORE, D
影响因子:
64.5
作者:
MELLON, P;PARKER, V;MANIATIS, T
通讯作者:
MANIATIS, T
影响因子:
64.5
作者:
GLUZMAN, Y
通讯作者:
GLUZMAN, Y
影响因子:
4.8
作者:
Chai, ZL;Brereton, P;Krozowski, Z
通讯作者:
Krozowski, Z