Tissue Inhibitor of Metalloproteinases (TIMP-1) Produced by Granulosa and Oviduct Cells Enhances in Vitro Development of Bovine Embryo1
Author(s) -
Takeshi Satoh,
Keizo Kobayashi,
Shoko Yamashita,
Makoto Kikuchi,
Yutaka Sendai,
Hiroyoshi Hoshi
Publication year - 1994
Publication title -
biology of reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.366
H-Index - 180
eISSN - 1529-7268
pISSN - 0006-3363
DOI - 10.1095/biolreprod50.4.835
Subject(s) - polyclonal antibodies , oviduct , biology , metalloproteinase , microbiology and biotechnology , western blot , matrix metalloproteinase , gel permeation chromatography , in vitro , complementary dna , biochemistry , antibody , chemistry , endocrinology , immunology , gene , organic chemistry , polymer
Embryogenesis-stimulating activity (ESA) was found in serum-free conditioned media (CM) of bovine cumulus/granulosa cells (BGC) and bovine oviductal epithelial cells (BOEC). The CM of BGC (BGC-CM) contained two molecular species of ESA, one with a low molecular weight (M(r) 30,000) and another with a high molecular weight (M(r) 80,000); but only the activity with low molecular weight was detected in CM of BOEC by gel-permeation chromatography. The smaller ESA (embryogenin-1) in BGC-CM was purified to homogeneity, as a common activity in both CM by a combination of gel-permeation chromatography, ion-exchange chromatography, and reverse-phase HPLC. Embryogenin-1 has a molecular weight of 31,100 (reduced) and has been identified as a bovine tissue inhibitor of metalloproteinase-1 by NH2-terminal amino acid sequence analysis. Western blot analysis, anti-proteinase activities against metalloproteinases, and the nucleotide sequence of cDNA isolated from a lambda gt11 cDNA library of the bovine ovary by a polyclonal antibody against embryogenin-1. These data suggest that the tissue inhibitor of metalloproteinase-1 produced by BGC and BOEC is a major ESA for in vitro development of bovine embryos.
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