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. 1969 Jun 1;41(3):716–735. doi: 10.1083/jcb.41.3.716

STUDIES ON THE HUMAN CORPUS LUTEUM

II. Observations on the Ultrastructure of Luteal Cells During Pregnancy

Eleanor C Adams 1, Arthur T Hertig 1
PMCID: PMC2107828  PMID: 5768871

Abstract

The ultrastructure of human corpora lutea obtained during the 6th, 10th, 16th, and 35th week of pregnancy is reported. Differences between the established luteal cell of pregnancy and the transitory luteal cell of the menstrual cycle are noted. In pregnancy the luteal cell is more compartmentalized into a peripheral mass of ER (endoplasmic reticulum) and a central area where mitochondria and Golgi complexes are concentrated. The latter area extends to a cell surface where microvilli face on a perivascular space. Long bundles of filaments are prominent within the luteal cell cytoplasm and, in contiguous cells, appear to arise from adjacent desmosomal regions. Bilateral subsurface cisternae of granular ER at lateral cell borders appear to be areas of specialized junctional surfaces. Certain luteal cells with irregular nuclear membranes are also characterized by vesicular aggregates enclosed within a single membrane. These aggregates are found within the peripheral nucleoplasm or the perinuclear cytoplasm. Their single limiting membrane often appears continuous with either the inner or outer leaflet of the nuclear membrane.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Green J. A., Garcilazo J. A., Maqueo M. Ultrastructure of the human ovary. II. The luteal cell at term. Am J Obstet Gynecol. 1967 Nov 15;99(6):855–863. doi: 10.1016/0002-9378(67)90400-0. [DOI] [PubMed] [Google Scholar]
  2. Jones A. L., Fawcett D. W. Hypertrophy of the agranular endoplasmic reticulum in hamster liver induced by phenobarbital (with a review on the functions of this organelle in liver). J Histochem Cytochem. 1966 Mar;14(3):215–232. doi: 10.1177/14.3.215. [DOI] [PubMed] [Google Scholar]
  3. Krishan A., Uzman B. G., Hedley-Whyte E. T. Nuclear bodies: a component of cell nuclei in hamster tissues and human tumors. J Ultrastruct Res. 1967 Aug 30;19(5):563–572. doi: 10.1016/s0022-5320(67)80082-0. [DOI] [PubMed] [Google Scholar]
  4. Miyai K., Steiner J. W. Fine structure of interphase liver cell nuclei in subacute ethionine intoxication. Exp Mol Pathol. 1965 Oct;4(5):525–566. doi: 10.1016/0014-4800(65)90016-x. [DOI] [PubMed] [Google Scholar]
  5. ROSENBLUTH J. Subsurface cisterns and their relationship to the neuronal plasma membrane. J Cell Biol. 1962 Jun;13:405–421. doi: 10.1083/jcb.13.3.405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Ryan K. J., Petro Z. Steroid biosynthesis by human ovarian granulosa and thecal cells. J Clin Endocrinol Metab. 1966 Jan;26(1):46–52. doi: 10.1210/jcem-26-1-46. [DOI] [PubMed] [Google Scholar]
  7. SAVARD K., MARSH J. M., RICE B. F. GONADOTROPINS AND OVARIAN STEROIDOGENESIS. Recent Prog Horm Res. 1965;21:285–365. [PubMed] [Google Scholar]
  8. WEBER A., WHIPP S., USENIK E., FROMMES S. STRUCTURAL CHANGES IN THE NUCLEAR BODY IN THE ADRENAL ZONA FASCICULATA OF THE CALF FOLLOWING THE ADMINISTRATION OF ACTH. J Ultrastruct Res. 1964 Dec;11:564–576. doi: 10.1016/s0022-5320(64)80082-4. [DOI] [PubMed] [Google Scholar]

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