Literature DB >> 9472949

Apoptosis during spontaneous luteolysis in the cyclic golden hamster: biochemical and morphological evidence.

J T McCormack1, M G Friederichs, S D Limback, G S Greenwald.   

Abstract

The corpora lutea (CL) of the cyclic hamster are destroyed between Days 2 and 3 of the 4-day estrous cycle so that only one set is ever present (Day 1 = estrus, Day 4 = proestrus). The possibility that luteal cell death in the cyclic hamster is attributable to apoptosis was explored. The earliest histological signs of structural luteolysis were detected at 0600 h of Day 3 as evidenced by a few scattered luteal cells displaying the characteristic morphology of apoptotic cells and by a massive infiltration of neutrophils. The peaks of neutrophil influx and luteal apoptosis were reached on Day 3, 1200 h, and Day 3, 2400 h, respectively. Thus, the increase in neutrophils occurs before the major onset of luteolysis. By Day 3, 2400 h, the CL had already shrunken one third by weight, and they virtually vanished by the next Day 1. Apoptosis ultimately destroyed luteal endothelial cells, luteal cells, and neutrophils. Electrophoretic analysis of low-molecular weight DNA in luteal cell lysates revealed a definite ladder pattern of oligonucleosomal-length DNA fragments--characteristic of apoptosis--on Day 3 beginning at 1200 h. The pattern was not detectable in CL collected on Day 2. Comparing Day 3 CL collected at 0900-1200 h with those at 1500-1800 h showed that only the latter group exhibited inter-nucleosomal cleavage activity. The minimal number of CL on Day 3, 1500 h, needed to demonstrate DNA laddering was six. In summary, the electrophoretic separation of oligonucleosomal fragments and histology indicated that apoptosis occurs during spontaneous luteal regression on Day 3 of the hamster cycle. The initiation of apoptosis is not apparent until several hours after the onset of functional luteolysis. The rapidity with which apoptosis eliminates the CL over a very precise time schedule makes the cyclic hamster an ideal model to analyze the factors involved in structural luteolysis.

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Year:  1998        PMID: 9472949     DOI: 10.1095/biolreprod58.1.255

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  9 in total

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2.  Enhancement and suppression of ultradian and circadian rhythms across the female hamster reproductive cycle.

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3.  Exogenous estradiol enhances apoptosis in regressing post-partum rat corpora lutea possibly mediated by prolactin.

Authors:  Alicia A Goyeneche; Carlos M Telleria
Journal:  Reprod Biol Endocrinol       Date:  2005-08-30       Impact factor: 5.211

4.  Progesterone is essential for protecting against LPS-induced pregnancy loss. LIF as a potential mediator of the anti-inflammatory effect of progesterone.

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Journal:  PLoS One       Date:  2013-02-07       Impact factor: 3.240

Review 5.  Cytokines and angiogenesis in the corpus luteum.

Authors:  António M Galvão; Graça Ferreira-Dias; Dariusz J Skarzynski
Journal:  Mediators Inflamm       Date:  2013-06-11       Impact factor: 4.711

6.  Prostaglandin F2alpha- and FAS-activating antibody-induced regression of the corpus luteum involves caspase-8 and is defective in caspase-3 deficient mice.

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Journal:  Reprod Biol Endocrinol       Date:  2003-02-11       Impact factor: 5.211

Review 7.  Microvascular endothelial cells of the corpus luteum.

Authors:  John S Davis; Bo R Rueda; Katherina Spanel-Borowski
Journal:  Reprod Biol Endocrinol       Date:  2003-11-10       Impact factor: 5.211

Review 8.  Angiogenesis in the corpus luteum.

Authors:  Hamish M Fraser; Christine Wulff
Journal:  Reprod Biol Endocrinol       Date:  2003-11-10       Impact factor: 5.211

9.  Apoptosis-Related Factors in the Luteal Phase of the Domestic Cat and Their Involvement in the Persistence of Corpora Lutea in Lynx.

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Journal:  PLoS One       Date:  2015-11-24       Impact factor: 3.240

  9 in total

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