[The "dystrophic" lime content in the normal human placenta].
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The DNA content of individual nuclei in four immature human placentas was determined by microspectrophotometric analysis of Feulgen-stained sections. The absence of mitosis in the syncytiotrophoblast, taken together with the finding of a diploid unimodal distribution, at a time of rapid placental growth, indicated that the syncytiotrophoblast possessed little or no intrinsic reproductive capacity. In contrast, the cytotrophoblast displayed considerable mitotic activity and was found to contain a high proportion of nuclei with DNA values in excess of the diploid amount, corresponding to DNA synthesis in interphase nuclei preparatory to division. From the complementary behavior of the two layers of trophoblast, with respect to evidence of reproductive ability, it is concluded that the rapid accumulation of nuclei in the syncytiotrophoblast, during the early development of the placenta, is accounted for by cell proliferation within the cytotrophoblast followed by alignment and coalescence of some daughter cells in the syncytiotrophoblast.
Through the use of immunohistochemical techniques, human chorionic gonadotropin has been localized to syncytiotrophoblastic cells of immature placenta, hydatidiform mole, chorioadenoma destruens, and choriocarcinoma. No gonadotropin has been detected in cytotrophoblast. Evidence is discussed which suggests that syncytiotrophoblast is the cell of origin of human chorionic gonadotropin. The observation that formalin fixation did not alter the ability of human chorionic gonadotropin to react with its specific antibody permitted the study of formalin-fixed paraffin-embedded tissues stored in the tissue collection. In addition, the excellence of histologic preparations following formalin fixation facilitated cytologic identification.
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