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Physiology · Reproduction: two-cell theory of oestrogen synthesis
Sample itemIn the follicular phase, theca interna cells under LH stimulation make androstenedione. Where is it converted to oestradiol, and under which hormone?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Granulosa cells, by aromatase induced by FSH
In the two-cell, two-gonadotrophin model, LH stimulates theca cells to make androgens. These diffuse into the granulosa cells, where FSH induces aromatase, which converts androstenedione to oestrone and testosterone to oestradiol. FSH also induces LH receptors on granulosa cells before ovulation.
Option by option
A. Corpus luteum cells, by 21-hydroxylase induced by hCG
21-hydroxylase is a step in corticosteroid synthesis, and hCG acts on the luteal body only in pregnancy.
B. Granulosa cells, by 5-alpha reductase induced by LH
5-alpha reductase makes dihydrotestosterone, not oestradiol.
C. Granulosa cells, by aromatase induced by FSH (correct)
FSH drives aromatase in granulosa cells, which complete oestradiol production.
D. Theca cells, by aromatase induced by LH
Theca cells lack significant aromatase, so they only supply androgen substrate.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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