The corpus luteum is a temporary endocrine structure formed from the ovarian follicle after ovulation. Its luteinized cells produce substantial progesterone, helping maintain the secretory state of the endometrium. Without sustained hormonal support it regresses; in early pregnancy, human chorionic gonadotropin helps preserve its steroid production.[ref]
It illustrates that an endocrine gland need not be a permanently separate organ. A local tissue is reorganized into a hormone-secreting structure and later changes again. A measured progesterone concentration reflects both this production and removal from the blood, so it is not a direct count of luteal cells.
A luteal cell is a biological cell belonging to the corpus luteum; in endocrine descriptions, the term usually emphasizes its steroid-producing populations. These cells arise as follicular tissue undergoes luteinization and contribute progesterone. The whole corpus luteum also contains vessels and other supporting cells, so an endocrine-cell count is not a count of every cell in the structure.[ref]
Functional diversity can persist within the steroid-producing population. In 1982, researchers separated larger and smaller luteal cells from sheep by a flow-based separation procedure. For equal cell counts, unstimulated progesterone release from the larger-cell preparation was about twenty times that from the smaller-cell preparation. The result concerns the tested ewe preparation and conditions, not a universal ratio for all mammals.[ref]
For an illustrative accounting model, ten cells each secreting one unit per hour and ten cells each secreting twenty units per hour contribute ten and two hundred units per hour respectively. Equal cell numbers need not imply equal endocrine contributions. Actual circulating progesterone additionally depends on distribution and removal from the blood.
Luteinization is the differentiation and reorganization of follicular cells into the steroid-secreting cells of the corpus luteum. Granulosa cells and theca cells change their endocrine activity, with increased capacity for progesterone production. In the normal ovarian cycle, the luteinizing hormone surge coordinates this process with ovulation. Release of the oocyte and transformation of the remaining follicular tissue are nevertheless distinct events.[ref]
A functional experiment examines what the differentiated cells actually make. In a 1991 study, human luteinized granulosa cells were cultured for 48 hours with or without human chorionic gonadotropin or follicle-stimulating hormone. The investigators measured several steroids and assayed aromatase activity separately. Progesterone production was prominent and responsive to stimulation, demonstrating endocrine activity in the luteinized preparation.[ref]
This motivates a useful distinction between cell state and one of its outputs. Increased progesterone is evidence of altered steroid production, but one concentration measurement does not by itself prove that a whole follicle has ruptured, that an oocyte was released, or that every structural step of luteinization occurred. Comparing histology with biochemical measurements makes the interpretation more precise.

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