{"id":{"repo_id":"uwo","oai_identifier":"oai:uwo.scholaris.ca:20.500.14721/20338"},"canonical_url":"https://search.dev.ndltd.org/etd/uwo/oai:uwo.scholaris.ca:20.500.14721/20338","repository":{"repo_id":"uwo","name":"Western University","base_url":"https://uwo.scholaris.ca/server/oai/request"},"display":{"title":"CONNECTIVE TISSUE GROWTH FACTOR IS REQUIRED FOR CHONDROGENESIS","abstract":"Connective tissue growth factor (CTGF, CCN2) is expressed by mesenchymal cells during development. Mice genetically deficient in CCN2 display severe bone defects and die immediately after birth. The molecular basis of this defect is not known. We've used in vitro models of chondrogenesis to show that CCN2 expression is induced during chondrogenesis, paralleling induction of known early chondrogenic markers (sox9, sox6, l-sox5, type II collagen, aggrecan, decorin and link protein). Real-Time PCR, Western blot and Immunofluorescence reveal that CCN2 is required for the early stages of chondrogenesis, including expression of sox6 and aggrecan, but not type II collagen. Furthermore, focal adhesion kinase (FAK) was found to be an upstream mediator of CCN2 expression and the absence of FAK promotes the process of chondrogenesis. Therefore, CCN2 is required for early chondrogenic events, downstream of FAK and is responsible for regulating components of the chondrogenic extracellular matrix.","abstract_html":"Connective tissue growth factor (CTGF, CCN2) is expressed by mesenchymal cells during development. Mice genetically deficient in CCN2 display severe bone defects and die immediately after birth. The molecular basis of this defect is not known. We've used in vitro models of chondrogenesis to show that CCN2 expression is induced during chondrogenesis, paralleling induction of known early chondrogenic markers (sox9, sox6, l-sox5, type II collagen, aggrecan, decorin and link protein). Real-Time PCR, Western blot and Immunofluorescence reveal that CCN2 is required for the early stages of chondrogenesis, including expression of sox6 and aggrecan, but not type II collagen. Furthermore, focal adhesion kinase (FAK) was found to be an upstream mediator of CCN2 expression and the absence of FAK promotes the process of chondrogenesis. Therefore, CCN2 is required for early chondrogenic events, downstream of FAK and is responsible for regulating components of the chondrogenic extracellular matrix.","abstract_has_math":false,"creators":["Pala, Daphne"],"institution":null,"degree_name":"M Sc","degree_level":null,"degree_discipline":"Physiology","degree_department":null,"school":null,"contributors":[],"advisors":["Leask, Andrew","Beier, Frank"],"committee_chairs":[],"committee_members":[],"year":2007,"date_issued":"2007-01-01","date_published":"2007-01-01","updated_at":"2026-07-27T21:55:59Z","subjects":["Chondrogenesis","Connective Tissue Growth Factor","Sox6","Aggrecan","Type II Collagen","Focal Adhesion Kinase","Gene Expression","Extracellular Matrix"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://hdl.handle.net/20.500.14721/20338","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Leask, Andrew","Beier, Frank"]},{"key":"dc:creator","label":"Author","values":["Pala, Daphne"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2025-06-25T19:21:30Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2025-06-25T19:21:30Z"]},{"key":"dc:date.issued","label":"Date","values":["2007-01-01"]},{"key":"dc:type","label":"Dc Type","values":["thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Physiology"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M Sc"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Chondrogenesis","Connective Tissue Growth Factor","Sox6","Aggrecan","Type II Collagen","Focal Adhesion Kinase","Gene Expression","Extracellular Matrix"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["https://hdl.handle.net/20.500.14721/20338"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Connective tissue growth factor (CTGF, CCN2) is expressed by mesenchymal cells during development. Mice genetically deficient in CCN2 display severe bone defects and die immediately after birth. The molecular basis of this defect is not known. We've used in vitro models of chondrogenesis to show that CCN2 expression is induced during chondrogenesis, paralleling induction of known early chondrogenic markers (sox9, sox6, l-sox5, type II collagen, aggrecan, decorin and link protein). Real-Time PCR, Western blot and Immunofluorescence reveal that CCN2 is required for the early stages of chondrogenesis, including expression of sox6 and aggrecan, but not type II collagen. Furthermore, focal adhesion kinase (FAK) was found to be an upstream mediator of CCN2 expression and the absence of FAK promotes the process of chondrogenesis. Therefore, CCN2 is required for early chondrogenic events, downstream of FAK and is responsible for regulating components of the chondrogenic extracellular matrix."]},{"key":"dc:title","label":"Title","values":["CONNECTIVE TISSUE GROWTH FACTOR IS REQUIRED FOR CHONDROGENESIS"]}]}],"canonical_facts":{"dc:contributor.advisor":["Leask, Andrew","Beier, Frank"],"dc:creator":["Pala, Daphne"],"dc:date.accessioned":["2025-06-25T19:21:30Z"],"dc:date.available":["2025-06-25T19:21:30Z"],"dc:date.issued":["2007-01-01"],"dc:description.abstract":["Connective tissue growth factor (CTGF, CCN2) is expressed by mesenchymal cells during development. Mice genetically deficient in CCN2 display severe bone defects and die immediately after birth. The molecular basis of this defect is not known. We've used in vitro models of chondrogenesis to show that CCN2 expression is induced during chondrogenesis, paralleling induction of known early chondrogenic markers (sox9, sox6, l-sox5, type II collagen, aggrecan, decorin and link protein). Real-Time PCR, Western blot and Immunofluorescence reveal that CCN2 is required for the early stages of chondrogenesis, including expression of sox6 and aggrecan, but not type II collagen. Furthermore, focal adhesion kinase (FAK) was found to be an upstream mediator of CCN2 expression and the absence of FAK promotes the process of chondrogenesis. Therefore, CCN2 is required for early chondrogenic events, downstream of FAK and is responsible for regulating components of the chondrogenic extracellular matrix."],"dc:identifier.uri":["https://hdl.handle.net/20.500.14721/20338"],"dc:subject":["Chondrogenesis","Connective Tissue Growth Factor","Sox6","Aggrecan","Type II Collagen","Focal Adhesion Kinase","Gene Expression","Extracellular Matrix"],"dc:title":["CONNECTIVE TISSUE GROWTH FACTOR IS REQUIRED FOR CHONDROGENESIS"],"dc:type":["thesis"],"thesis:degree_discipline":["Physiology"],"thesis:degree_name":["M Sc"]},"updated_at":"2026-07-27T21:55:59Z"}