Two Distinct Populations of Tumor Necrosis Factor-Stimulated Gene-6 Protein in the Extracellular Matrix of Expanded Mouse Cumulus Cell–Oocyte Complexes

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-α-trypsin inhibitor (IαI) family....

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Veröffentlicht in:Archives of biochemistry and biophysics 2001-10, Vol.394 (2), p.173-181
Hauptverfasser: Mukhopadhyay, Durba, Hascall, Vincent C., Day, Anthony J., Salustri, Antonietta, Fülöp, Csaba
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container_issue 2
container_start_page 173
container_title Archives of biochemistry and biophysics
container_volume 394
creator Mukhopadhyay, Durba
Hascall, Vincent C.
Day, Anthony J.
Salustri, Antonietta
Fülöp, Csaba
description 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-α-trypsin inhibitor (IαI) 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 ∼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 IαI 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.
doi_str_mv 10.1006/abbi.2001.2552
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subjects Alpha-Globulins - chemistry
Alpha-Globulins - genetics
Alpha-Globulins - metabolism
Amino Acid Sequence
Animals
Blotting, Western
Cell Adhesion Molecules - chemistry
Cell Adhesion Molecules - genetics
Cell Adhesion Molecules - metabolism
Cell Differentiation
Cells, Cultured
cumulus cell-oocyte complex
extracellular matrix
Extracellular Matrix - chemistry
Extracellular Matrix - metabolism
Female
Follicular Phase
hyaluronan
Hyaluronic Acid - metabolism
Immunohistochemistry
inter-α-trypsin inhibitor
Macromolecular Substances
Mass Spectrometry
Mice
Molecular Sequence Data
Molecular Weight
Oocytes - cytology
Oocytes - drug effects
Oocytes - metabolism
Ovarian Follicle - cytology
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - metabolism
Sequence Analysis, Protein
tumor necrosis factor-stimulated gene-6
Up-Regulation
title Two Distinct Populations of Tumor Necrosis Factor-Stimulated Gene-6 Protein in the Extracellular Matrix of Expanded Mouse Cumulus Cell–Oocyte Complexes
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