Apoptosis in bovine granulosa cells in relation to steroid synthesis, cyclic adenosine 3',55'-monophosphate response to follicle-stimulating hormone and luteinizing hormone, and follicular atresia

Apoptosis is a process of selective cell deletion implicated as a mechanism underlying the process of ovarian follicular atresia The aims of this study were 1) to test the hypothesis that granulosa cell death during follicular (greater than or equal to 4-mm diameter) atresia in cows occurs by apopto...

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Veröffentlicht in:Biology of reproduction 1994, Vol.51
Hauptverfasser: Jolly P.D, Tisdall D.J, Heath D.A, Lun S, McNatty K.P
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container_title Biology of reproduction
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creator Jolly P.D
Tisdall D.J
Heath D.A
Lun S
McNatty K.P
description Apoptosis is a process of selective cell deletion implicated as a mechanism underlying the process of ovarian follicular atresia The aims of this study were 1) to test the hypothesis that granulosa cell death during follicular (greater than or equal to 4-mm diameter) atresia in cows occurs by apoptosis and 2) to define relationships between the occurrence and degree of granulosa cell apoptosis, cAMP response to FSH or LH, extant aromatase activity, and other previously established biochemical and morphometric indices of granulosa cell function and follicular atresia in this species. Granulosa cells and follicular fluid from individual follicles 4-18 mm in diameter were collected from luteal-phase cow ovaries. Follicles were classified by morphometric criteria as "healthy" (n = 45) or atretic (n 34). Apoptosis in granulosa cells from each follicle was inferred from detection of internucleosomal DNA cleavage by 3'-end radiolabeling; it was quantitated both subjectively from intensity of oligonucleosome labeling (apoptosis [AP] score = 0, 1, 2, or 3) and objectively by beta-counting of low-molecular-weight gel fragments (labeling index; LI). Extant aromatase activity (ng estradiol produced/10(6) cells/3 h) and cAMP response (pmol/10(6) cells) to different doses of FSH or LH (1-10000 ng/ml) was determined for granulosa cells from most healthy follicles (n = 39). Apoptosis was detected in granulosa cells from all atretic follicles as well as from 76% of healthy follicles, from 80% (16 of 20) of follicles with follicular fluid estradiol to progesterone ratios > 1, and from 71% (10 of 14) of follicles with extant aromatase activity (> 2 ng/10(6) cells/3 h). For healthy and atretic follicles, degree of DNA fragmentation was inversely related to the number of granulosa cells recovered (as percentage maximum by follicle size).
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Granulosa cells and follicular fluid from individual follicles 4-18 mm in diameter were collected from luteal-phase cow ovaries. Follicles were classified by morphometric criteria as "healthy" (n = 45) or atretic (n 34). Apoptosis in granulosa cells from each follicle was inferred from detection of internucleosomal DNA cleavage by 3'-end radiolabeling; it was quantitated both subjectively from intensity of oligonucleosome labeling (apoptosis [AP] score = 0, 1, 2, or 3) and objectively by beta-counting of low-molecular-weight gel fragments (labeling index; LI). Extant aromatase activity (ng estradiol produced/10(6) cells/3 h) and cAMP response (pmol/10(6) cells) to different doses of FSH or LH (1-10000 ng/ml) was determined for granulosa cells from most healthy follicles (n = 39). Apoptosis was detected in granulosa cells from all atretic follicles as well as from 76% of healthy follicles, from 80% (16 of 20) of follicles with follicular fluid estradiol to progesterone ratios &gt; 1, and from 71% (10 of 14) of follicles with extant aromatase activity (&gt; 2 ng/10(6) cells/3 h). 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Granulosa cells and follicular fluid from individual follicles 4-18 mm in diameter were collected from luteal-phase cow ovaries. Follicles were classified by morphometric criteria as "healthy" (n = 45) or atretic (n 34). Apoptosis in granulosa cells from each follicle was inferred from detection of internucleosomal DNA cleavage by 3'-end radiolabeling; it was quantitated both subjectively from intensity of oligonucleosome labeling (apoptosis [AP] score = 0, 1, 2, or 3) and objectively by beta-counting of low-molecular-weight gel fragments (labeling index; LI). Extant aromatase activity (ng estradiol produced/10(6) cells/3 h) and cAMP response (pmol/10(6) cells) to different doses of FSH or LH (1-10000 ng/ml) was determined for granulosa cells from most healthy follicles (n = 39). Apoptosis was detected in granulosa cells from all atretic follicles as well as from 76% of healthy follicles, from 80% (16 of 20) of follicles with follicular fluid estradiol to progesterone ratios &gt; 1, and from 71% (10 of 14) of follicles with extant aromatase activity (&gt; 2 ng/10(6) cells/3 h). 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Granulosa cells and follicular fluid from individual follicles 4-18 mm in diameter were collected from luteal-phase cow ovaries. Follicles were classified by morphometric criteria as "healthy" (n = 45) or atretic (n 34). Apoptosis in granulosa cells from each follicle was inferred from detection of internucleosomal DNA cleavage by 3'-end radiolabeling; it was quantitated both subjectively from intensity of oligonucleosome labeling (apoptosis [AP] score = 0, 1, 2, or 3) and objectively by beta-counting of low-molecular-weight gel fragments (labeling index; LI). Extant aromatase activity (ng estradiol produced/10(6) cells/3 h) and cAMP response (pmol/10(6) cells) to different doses of FSH or LH (1-10000 ng/ml) was determined for granulosa cells from most healthy follicles (n = 39). Apoptosis was detected in granulosa cells from all atretic follicles as well as from 76% of healthy follicles, from 80% (16 of 20) of follicles with follicular fluid estradiol to progesterone ratios &gt; 1, and from 71% (10 of 14) of follicles with extant aromatase activity (&gt; 2 ng/10(6) cells/3 h). For healthy and atretic follicles, degree of DNA fragmentation was inversely related to the number of granulosa cells recovered (as percentage maximum by follicle size).</abstract></addata></record>
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source Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects adenosine monophosphate
adenosinmonofosfato
adn
bovin
cattle
cells
cellule
celulas
cows
death
dna
estrogenos
fsh
ganado bovino
hfs
malformacion
malformation
malformations
metabolisme des steroides
metabolismo de esteroides
metalloproteine
metalloproteins
metalproteinas
mort
muerte
oestrogene
oestrogens
ovaire
ovaries
ovarios
oxidoreductases
oxidorreductasas
oxydoreductase
progesterona
progesterone
steroid metabolism
vaca
vache
title Apoptosis in bovine granulosa cells in relation to steroid synthesis, cyclic adenosine 3',55'-monophosphate response to follicle-stimulating hormone and luteinizing hormone, and follicular atresia
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