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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0010092,
umls-concept:C0017262,
umls-concept:C0018120,
umls-concept:C0035696,
umls-concept:C0040300,
umls-concept:C0185117,
umls-concept:C0221971,
umls-concept:C0679058,
umls-concept:C1123019,
umls-concept:C1547699,
umls-concept:C1571705,
umls-concept:C1999216,
umls-concept:C2700640,
umls-concept:C2911684
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pubmed:issue |
2
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pubmed:dateCreated |
1995-3-2
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pubmed:abstractText |
Metalloproteinase inhibitors, such as tissue inhibitors of metalloproteinases 1 and 2 (TIMP-1 and -2), play a key role in the regulation of metalloproteinases that modify extracellular matrix composition. Although expression of TIMP-1 within ovarian tissues has been well characterized, little information is available regarding expression of TIMP-2. The objective of the present studies was to characterize the ontogeny and localization of TIMP-2 messenger RNA (mRNA) within ovine preovulatory follicles and luteal tissue. Total cellular RNA was isolated from preovulatory follicles collected before (presurge; n = 3), or 12-14 h after (post surge; n = 4) an LHRH-induced gonadotropin surge, and from luteal tissue collected on days 3, 7, 10, 13, and 16 post estrus (n = 5, 5, 4, 5, and 5, respectively). TIMP-2 mRNA was expressed by both presurge and postsurge follicles, and expression did not increase after the gonadotropin surge (P = 0.44). In situ hybridization localized TIMP-2 mRNA primarily to the thecal layer of post-surge follicles (n = 3). TIMP-2 mRNA was also localized in a heterogeneous distribution within corpora lutea collected on days 3 and 10 post estrus (n = 3 each). Concentrations of TIMP-2 mRNA (picograms per microgram tissue DNA) were greater in corpora lutea collected during the early luteal phase (days 3 and 7) than the late luteal phase (day 16; P < 0.05). TIMP-2 mRNA was detected in purified populations of both small (n = 4) and large (n = 3) luteal cells, and mRNA concentrations (picograms per microgram DNA) were greater in the large luteal cells (P < or = 0.0002). In addition, immunoreactive TIMP-2 (approximately 21,000 M(r)) was detected by Western blot analysis of ovine luteal cell secreted proteins. We conclude that 1) TIMP-2 mRNA is expressed by the thecal layer of ovine preovulatory follicles and expression is not increased by the preovulatory gonadotropin surge; 2) expression of TIMP-2 mRNA is maximal during the early luteal phase; and 3) expression of TIMP-2 mRNA is greatest in large luteal cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0013-7227
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
136
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
570-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7835290-Animals,
pubmed-meshheading:7835290-Blotting, Western,
pubmed-meshheading:7835290-Cattle,
pubmed-meshheading:7835290-Cells, Cultured,
pubmed-meshheading:7835290-Corpus Luteum,
pubmed-meshheading:7835290-Estrus,
pubmed-meshheading:7835290-Female,
pubmed-meshheading:7835290-Gonadotropins,
pubmed-meshheading:7835290-In Situ Hybridization,
pubmed-meshheading:7835290-Luteal Cells,
pubmed-meshheading:7835290-Luteal Phase,
pubmed-meshheading:7835290-Metalloendopeptidases,
pubmed-meshheading:7835290-Ovarian Follicle,
pubmed-meshheading:7835290-Protein Biosynthesis,
pubmed-meshheading:7835290-RNA, Messenger,
pubmed-meshheading:7835290-Sheep,
pubmed-meshheading:7835290-Tissue Inhibitor of Metalloproteinase-2
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pubmed:year |
1995
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pubmed:articleTitle |
Expression of messenger ribonucleic acid encoding tissue inhibitor of metalloproteinases-2 within ovine follicles and corpora lutea.
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pubmed:affiliation |
Department of Animal Science, University of Missouri, Columbia 65211.
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pubmed:publicationType |
Journal Article
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