Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (15)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Morales, C.
Right arrow Articles by Gaytán, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Morales, C.
Right arrow Articles by Gaytán, F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol. 15, No. 10, 2119-2128, October 2000
© 2000 European Society of Human Reproduction and Embryology

Different patterns of structural luteolysis in the human corpus luteum of menstruation

Concepción Morales1, Lourdes García-Pardo1, Carlos Reymundo1, Carmen Bellido2, José Eugenio Sánchez-Criado2 and Francisco Gaytán2,3

1 Departments of Pathology and 2 Cell Biology, Physiology and Immunology, Faculty of Medicine, University of Córdoba, Córdoba, Spain

Structural luteolysis is a complex process responsible for the elimination of the corpus luteum (CL). The aim of this study was to analyse the luteolytic process of the CL of menstruation. For this, we have morphologically studied 654 ovaries from 340 cycling women. Apoptotic cells were observed almost exclusively during the perimenstrual period and were extremely scarce at advanced stages of involution. Steroidogenic luteal cells surviving to the perimenstrual apoptotic wave underwent characteristic degenerative changes, consisting of intense cytoplasmic vacuolation, expression of macrophage markers and accumulation of lipofuscin pigment, and they persisted for long periods of time. Accumulation of corpora albicantia (CA) was observed in only 25% of a subset of 168 women, whereas 28% showed involuting CL without hyalinization, consisting of clusters of pigment-filled cells, and 46.4% showed ovaries with a mixture of CA and involuting CL without hyalinization or involuting CL with intermediate features. Evolution of the CL towards CA seemed to be related to the presence of a large, blood-filled cavity. The data from this study suggested that different patterns of structural luteolysis exist during CL involution, and that the final fate of the involuting CL is dependent on the presence of a large, central, blood-filled cavity.

Key words: apoptosis/cell death/corpus albicans/corpus luteum/structural luteolysis

3 To whom correspondence should be addressed at: Department of Cell Biology, Physiology and Immunology, Faculty of Medicine, University of Córdoba, 14004-Córdoba, Spain.E-mail: fi1begac{at}lucano.uco.es


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum ReprodHome page
I. Ben-Ami, L. Armon, S. Freimann, D. Strassburger, R. Ron-El, and A. Amsterdam
EGF-like growth factors as LH mediators in the human corpus luteum
Hum. Reprod., January 1, 2009; 24(1): 176 - 184.
[Abstract] [Full Text] [PDF]


Home page
Toxicol PatholHome page
E. Buse, M. Zoller, and E. Van Esch
The Macaque Ovary, with Special Reference to the Cynomolgus Macaque (Macaca fascicularis)
Toxicol Pathol, December 1, 2008; 36(7_suppl): 24S - 66S.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
F. Del Canto, W. Sierralta, P. Kohen, A. Munoz, J. F. Strauss III, and L. Devoto
Features of Natural and Gonadotropin-Releasing Hormone Antagonist-Induced Corpus Luteum Regression and Effects of in Vivo Human Chorionic Gonadotropin
J. Clin. Endocrinol. Metab., November 1, 2007; 92(11): 4436 - 4443.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
C. Stocco, C. Telleria, and G. Gibori
The Molecular Control of Corpus Luteum Formation, Function, and Regression
Endocr. Rev., February 1, 2007; 28(1): 117 - 149.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
H. M Fraser, H. Wilson, C. Wulff, J. S Rudge, and S. J Wiegand
Administration of vascular endothelial growth factor Trap during the 'post-angiogenic' period of the luteal phase causes rapid functional luteolysis and selective endothelial cell death in the marmoset.
Reproduction, October 1, 2006; 132(4): 589 - 600.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
J Aguilar, H M Fraser, H Wilson, E Clutton, D J Shaw, and E D Watson
Temporal relationship between proliferating and apoptotic hormone-producing and endothelial cells in the equine corpus luteum
Reproduction, July 1, 2006; 132(1): 111 - 118.
[Abstract] [Full Text] [PDF]


Home page
ReproductionHome page
A. A Goyeneche, J. M Harmon, and C. M Telleria
Cell death induced by serum deprivation in luteal cells involves the intrinsic pathway of apoptosis
Reproduction, January 1, 2006; 131(1): 103 - 111.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
B. Pan, K. Sengoku, K. Goishi, N. Takuma, T. Yamashita, K. Wada, and M. Ishikawa
The soluble and membrane-anchored forms of heparin-binding epidermal growth factor-like growth factor appear to play opposing roles in the survival and apoptosis of human luteinized granulosa cells
Mol. Hum. Reprod., August 1, 2002; 8(8): 734 - 741.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
S.F. Lunn, H.M. Fraser, and H.D. Mason
Structure of the corpus luteum in the ovulatory polycystic ovary
Hum. Reprod., January 1, 2002; 17(1): 111 - 117.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.