After the luteinizing hormone surge, the cumulus cell-oocyte complexes (COCs) in the preovulatory follicles produce a viscoelastic extracellular matrix, a process that requires the synthesis of hyaluronan as well as the incorporation of some components of the inter-alpha-trypsin inhibitor (IalphaI) family. In this study we report, that a hyaluronan-binding protein, the translated product of tumor necrosis factor-stimulated gene-6 (TSG-6), is also specifically accumulated in this matrix. TSG-6 mRNA expression is quickly upregulated and peaks at approximately 1500 copies/cell 4 h after the ovulatory stimuli as assessed by quantitative reverse transcription-polymerase chain reaction. Immunohistochemistry reveals the colocalization of the TSG-6 protein and hyaluronan around the cumulus and granulosa cells. The TSG-6 protein exists in two distinct populations in the COC matrix as demonstrated by Western-blot analysis. One population is a monomer that is anchored to the matrix by a noncovalent interaction. The second population is a covalent complex with either of the heavy chains of IalphaI and is bound to hyaluronan through a strong interaction that is resistant to denaturing conditions. The specific incorporation of the TSG-6 protein into the COC matrix suggests a structural role for this molecule.

Mukhopadhyay, D., Hascall, V., Day, A., Salustri, A., Fülöp, C. (2001). Two distinct populations of tumor necrosis factor-stimulated gene-6 protein in the extracellular matrix of expanded mouse cumulus cell-oocyte complexes. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 394(2), 173-181 [10.1006/abbi.2001.2552].

Two distinct populations of tumor necrosis factor-stimulated gene-6 protein in the extracellular matrix of expanded mouse cumulus cell-oocyte complexes

SALUSTRI, ANTONIETTA;
2001-10-15

Abstract

After the luteinizing hormone surge, the cumulus cell-oocyte complexes (COCs) in the preovulatory follicles produce a viscoelastic extracellular matrix, a process that requires the synthesis of hyaluronan as well as the incorporation of some components of the inter-alpha-trypsin inhibitor (IalphaI) family. In this study we report, that a hyaluronan-binding protein, the translated product of tumor necrosis factor-stimulated gene-6 (TSG-6), is also specifically accumulated in this matrix. TSG-6 mRNA expression is quickly upregulated and peaks at approximately 1500 copies/cell 4 h after the ovulatory stimuli as assessed by quantitative reverse transcription-polymerase chain reaction. Immunohistochemistry reveals the colocalization of the TSG-6 protein and hyaluronan around the cumulus and granulosa cells. The TSG-6 protein exists in two distinct populations in the COC matrix as demonstrated by Western-blot analysis. One population is a monomer that is anchored to the matrix by a noncovalent interaction. The second population is a covalent complex with either of the heavy chains of IalphaI and is bound to hyaluronan through a strong interaction that is resistant to denaturing conditions. The specific incorporation of the TSG-6 protein into the COC matrix suggests a structural role for this molecule.
15-ott-2001
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore BIO/17 - ISTOLOGIA
English
Con Impact Factor ISI
Mass Spectrometry; Animals; Follicular Phase; Hyaluronic Acid; Cell Differentiation; Mice; Amino Acid Sequence; Reverse Transcriptase Polymerase Chain Reaction; Cell Adhesion Molecules; Molecular Weight; Sequence Analysis, Protein; RNA, Messenger; Macromolecular Substances; Blotting, Western; Cells, Cultured; Ovarian Follicle; Extracellular Matrix; Molecular Sequence Data; Oocytes; Up-Regulation; Alpha-Globulins; Immunohistochemistry; Female
Mukhopadhyay, D., Hascall, V., Day, A., Salustri, A., Fülöp, C. (2001). Two distinct populations of tumor necrosis factor-stimulated gene-6 protein in the extracellular matrix of expanded mouse cumulus cell-oocyte complexes. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 394(2), 173-181 [10.1006/abbi.2001.2552].
Mukhopadhyay, D; Hascall, V; Day, A; Salustri, A; Fülöp, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/67102
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