@article{Rosenzweig2017240,
  abstract = {Autologous NP cell implantation is a potential therapeutic avenue for intervertebral disc (IVD) degeneration. However, monolayer expansion of cells isolated from surgical samples may negatively impact matrix production by way of dedifferentiation. Previously, we have used a continuous expansion culture system to successfully preserve a chondrocyte phenotype. In this work, we hypothesised that continuous expansion culture could also preserve nucleus pulposus (NP) phenotype. We confirmed that serial passaging drove NP dedifferentiation by significantly decreasing collagen type II, aggrecan and chondroadherin (CHAD) gene expression, compared to freshly isolated cells. Proliferation, gene expression profile and matrix production in both culture conditions were compared using primary bovine NP cells. Both standard culture and continuous culture produced clinically relevant cell populations. However, continuous culture cells maintained significantly higher collagen type II, aggrecan and CHAD transcript expression levels. Also, continuous expansion cells generated greater amounts of proteoglycan, collagen type II and aggrecan protein deposition in pellet cultures. To our surprise, continuous expansion of human intervertebral disc cells – isolated from acute herniation tissue – produced less collagen type II, aggrecan and CHAD genes and proteins, compared to standard culture. Also, continuous culture of cells isolated from young non-degenerate tissue did not preserve gene and protein expression, compared to standard culture. These data indicated that primary bovine and human NP cells responded differently to continuous culture, where the positive effects observed for bovine cells did not translate to human cells. Therefore, caution must be exercised when choosing animal models and cell sources for pre-clinical studies.},
  annote = {cited By 7},
  author = {Rosenzweig, D. H. and {Tremblay Gravel}, J. and Bisson, D. and Ouellet, J. A. and Weber, M. H. and Haglund, Lisbet},
  doi = {10.22203/eCM.v033a18},
  issn = {14732262},
  journal = {European Cells and Materials},
  keywords = {Cell culture,Elastic culture surfaces,Intervertebral disc,Nucleus pulposus cells,Tissue engineering},
  pages = {240--251},
  title = {{Comparative analysis in continuous expansion of bovine and human primary nucleus pulposus cells for tissue repair applications}},
  volume = {33},
  year = {2017}
  }

{"_id":"66QqnMCWBGQvDjjdM","bibbaseid":"rosenzweig-tremblaygravel-bisson-ouellet-weber-haglund-comparativeanalysisincontinuousexpansionofbovineandhumanprimarynucleuspulposuscellsfortissuerepairapplications-2017","authorIDs":["7AZ96jedDgXtbS2gZ","Aatxv2tJWMncBRk2u","GCSP5Bv7HRSfvTgtF","HjeQr6ipAQDCTb34Y","JXLnXyXovDQzK8jhE","QZJeRuRbo2f3Tktid","QftFYMfuBhvSrqkqw","RE87xEGJag3ckDR39","YmjqcmFRu2TrTQikj","soZgPGDyH8ywPF7Wh","yLsyWNQShJByQdMwZ","yYsb2kRc5GjCKdqk3"],"author_short":["Rosenzweig, D. H.","Tremblay Gravel, J.","Bisson, D.","Ouellet, J. A.","Weber, M. H.","Haglund, L."],"bibdata":{"bibtype":"article","type":"article","abstract":"Autologous NP cell implantation is a potential therapeutic avenue for intervertebral disc (IVD) degeneration. However, monolayer expansion of cells isolated from surgical samples may negatively impact matrix production by way of dedifferentiation. Previously, we have used a continuous expansion culture system to successfully preserve a chondrocyte phenotype. In this work, we hypothesised that continuous expansion culture could also preserve nucleus pulposus (NP) phenotype. We confirmed that serial passaging drove NP dedifferentiation by significantly decreasing collagen type II, aggrecan and chondroadherin (CHAD) gene expression, compared to freshly isolated cells. Proliferation, gene expression profile and matrix production in both culture conditions were compared using primary bovine NP cells. Both standard culture and continuous culture produced clinically relevant cell populations. However, continuous culture cells maintained significantly higher collagen type II, aggrecan and CHAD transcript expression levels. Also, continuous expansion cells generated greater amounts of proteoglycan, collagen type II and aggrecan protein deposition in pellet cultures. To our surprise, continuous expansion of human intervertebral disc cells – isolated from acute herniation tissue – produced less collagen type II, aggrecan and CHAD genes and proteins, compared to standard culture. Also, continuous culture of cells isolated from young non-degenerate tissue did not preserve gene and protein expression, compared to standard culture. These data indicated that primary bovine and human NP cells responded differently to continuous culture, where the positive effects observed for bovine cells did not translate to human cells. Therefore, caution must be exercised when choosing animal models and cell sources for pre-clinical studies.","annote":"cited By 7","author":[{"propositions":[],"lastnames":["Rosenzweig"],"firstnames":["D.","H."],"suffixes":[]},{"propositions":[],"lastnames":["Tremblay Gravel"],"firstnames":["J."],"suffixes":[]},{"propositions":[],"lastnames":["Bisson"],"firstnames":["D."],"suffixes":[]},{"propositions":[],"lastnames":["Ouellet"],"firstnames":["J.","A."],"suffixes":[]},{"propositions":[],"lastnames":["Weber"],"firstnames":["M.","H."],"suffixes":[]},{"propositions":[],"lastnames":["Haglund"],"firstnames":["Lisbet"],"suffixes":[]}],"doi":"10.22203/eCM.v033a18","issn":"14732262","journal":"European Cells and Materials","keywords":"Cell culture,Elastic culture surfaces,Intervertebral disc,Nucleus pulposus cells,Tissue engineering","pages":"240–251","title":"Comparative analysis in continuous expansion of bovine and human primary nucleus pulposus cells for tissue repair applications","volume":"33","year":"2017","bibtex":"@article{Rosenzweig2017240,\n abstract = {Autologous NP cell implantation is a potential therapeutic avenue for intervertebral disc (IVD) degeneration. However, monolayer expansion of cells isolated from surgical samples may negatively impact matrix production by way of dedifferentiation. Previously, we have used a continuous expansion culture system to successfully preserve a chondrocyte phenotype. In this work, we hypothesised that continuous expansion culture could also preserve nucleus pulposus (NP) phenotype. We confirmed that serial passaging drove NP dedifferentiation by significantly decreasing collagen type II, aggrecan and chondroadherin (CHAD) gene expression, compared to freshly isolated cells. Proliferation, gene expression profile and matrix production in both culture conditions were compared using primary bovine NP cells. Both standard culture and continuous culture produced clinically relevant cell populations. However, continuous culture cells maintained significantly higher collagen type II, aggrecan and CHAD transcript expression levels. Also, continuous expansion cells generated greater amounts of proteoglycan, collagen type II and aggrecan protein deposition in pellet cultures. To our surprise, continuous expansion of human intervertebral disc cells – isolated from acute herniation tissue – produced less collagen type II, aggrecan and CHAD genes and proteins, compared to standard culture. Also, continuous culture of cells isolated from young non-degenerate tissue did not preserve gene and protein expression, compared to standard culture. These data indicated that primary bovine and human NP cells responded differently to continuous culture, where the positive effects observed for bovine cells did not translate to human cells. Therefore, caution must be exercised when choosing animal models and cell sources for pre-clinical studies.},\n annote = {cited By 7},\n author = {Rosenzweig, D. H. and {Tremblay Gravel}, J. and Bisson, D. and Ouellet, J. A. and Weber, M. H. and Haglund, Lisbet},\n doi = {10.22203/eCM.v033a18},\n issn = {14732262},\n journal = {European Cells and Materials},\n keywords = {Cell culture,Elastic culture surfaces,Intervertebral disc,Nucleus pulposus cells,Tissue engineering},\n pages = {240--251},\n title = {{Comparative analysis in continuous expansion of bovine and human primary nucleus pulposus cells for tissue repair applications}},\n volume = {33},\n year = {2017}\n }\n ","author_short":["Rosenzweig, D. H.","Tremblay Gravel, J.","Bisson, D.","Ouellet, J. A.","Weber, M. H.","Haglund, L."],"key":"Rosenzweig2017240","id":"Rosenzweig2017240","bibbaseid":"rosenzweig-tremblaygravel-bisson-ouellet-weber-haglund-comparativeanalysisincontinuousexpansionofbovineandhumanprimarynucleuspulposuscellsfortissuerepairapplications-2017","role":"author","urls":{},"keyword":["Cell culture","Elastic culture surfaces","Intervertebral disc","Nucleus pulposus cells","Tissue engineering"],"metadata":{"authorlinks":{"rosenzweig, d":"https://rosenzweiglab.com/publication/"}},"downloads":0},"bibtype":"article","creationDate":"2020-05-22T18:05:19.863Z","downloads":0,"keywords":["cell culture","elastic culture surfaces","intervertebral disc","nucleus pulposus cells","tissue engineering"],"search_terms":["comparative","analysis","continuous","expansion","bovine","human","primary","nucleus","pulposus","cells","tissue","repair","applications","rosenzweig","tremblay gravel","bisson","ouellet","weber","haglund"],"title":"Comparative analysis in continuous expansion of bovine and human primary nucleus pulposus cells for tissue repair applications","year":2017,"biburl":"https://raw.githubusercontent.com/rosenzweiglab/rosenzweiglab.github.io/master/docs/references.bib","dataSources":["2AaMQS2PLCP3KCSxQ"]}