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. 2022 Nov 1;63(12):100309. doi: 10.1016/j.jlr.2022.100309

Fig. 6.

Fig. 6

Gonadal steroid production in control and seipin KO mice. A: Serum testosterone in control and seipin KO male mice. Male control (n = 8) and seipin KO mice (n = 8) were treated with hCG (2.5 IU per mouse), and serum was collected before and 4 h after the treatment for measurement of testosterone. B: Progesterone production in control and seipin KO female mice. Female control (n = 8) and seipin KO mice (n = 8) were treated with PMSG/eCG (2.5 IU per mouse), and serum was collected before and 5 h after the treatment for measurement of progesterone. C: Testosterone production in isolated Leydig cells. Leydig cells were isolated from control (n = 8) and seipin KO mice (n = 8) using Percoll gradients as described in the Materials and methods section. Freshly purified Leydig cells were incubated with 2.5 mM Bt2cAMP in the absence or presence of h-HDL3 (500 μg cholesterol/ml). After 5 h incubation, testosterone levels in the media were measured. D: Progesterone production in isolated granulosa cells. Age-matched female control (n = 8) and seipin KO mice (n = 8) were injected twice with 5 IU PMSG for 48 h. Granulosa cells were then isolated as described in the Materials and methods section. Freshly purified granulosa cells were incubated with 2.5 mM Bt2cAMP in the absence or presence of h-HDL3 (500 μg cholesterol/ml). After 5 h incubation, progesterone levels in the media were measured. Data are expressed as mean ± SEM. ∗P < 0.05; ∗∗P < 0.01.