A New Porcine In Vivo Animal Model of Disc Degeneration: Response of Anulus Fibrosus Cells, Chondrocyte-Like Nucleus Pulposus Cells, and Notochordal Nucleus Pulposus Cells to Partial Nucleotomy
In vivo animal study. To describe a new porcine disc degeneration model, and to analyze disc remodeling and degeneration after nucleotomy with special view to the different nucleus pulposus (NP) cell types. Thus far, predominantly smaller animals were used for disc degeneration models; however, such...
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creator | OMLOR, Georg W NERLICH, Andreas G WILKE, Hans-Joachim PFEIFFER, Michael LORENZ, Helga SCHAAF-KEIM, Markus BERTRAM, Helge RICHTER, Wiltrud CARSTENS, Claus GUEHRING, Thorsten |
description | In vivo animal study.
To describe a new porcine disc degeneration model, and to analyze disc remodeling and degeneration after nucleotomy with special view to the different nucleus pulposus (NP) cell types.
Thus far, predominantly smaller animals were used for disc degeneration models; however, such small discs were inappropriate to investigate cell implementation therapies. Though notochordal cells (NCs) are important for disc formation and maintenance, differences in the amount of NCs between human and animal discs have often been neglected.
Twenty-four Goettingen minipigs underwent partial nucleotomy with a 16G biopsy cannula, to remove approximately 10% of total NP volume. Animals were followed up for 3, or 24 weeks and analyzed by radiographs, MRIs, (immuno)histology, gene expression analysis, and biomechanical testing.
Three weeks after nucleotomy disc height was reduced by 26%, and magnetic resonance imaging signal intensity by 40%. At 24 weeks disc height was decreased by 32%. Increased degenerative changes were found in a histodegeneration score 3 and 24 weeks after nucleotomy, as well as considerable NP scarification after 3 weeks. In controls, cytokeratin-8 immunohistochemistry identified NCs in proximity to chondrocyte-like NP cells at approximately equal ratio. After nucleotomy, NCs were considerably reduced to |
doi_str_mv | 10.1097/BRS.0b013e3181b723c9 |
format | Article |
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To describe a new porcine disc degeneration model, and to analyze disc remodeling and degeneration after nucleotomy with special view to the different nucleus pulposus (NP) cell types.
Thus far, predominantly smaller animals were used for disc degeneration models; however, such small discs were inappropriate to investigate cell implementation therapies. Though notochordal cells (NCs) are important for disc formation and maintenance, differences in the amount of NCs between human and animal discs have often been neglected.
Twenty-four Goettingen minipigs underwent partial nucleotomy with a 16G biopsy cannula, to remove approximately 10% of total NP volume. Animals were followed up for 3, or 24 weeks and analyzed by radiographs, MRIs, (immuno)histology, gene expression analysis, and biomechanical testing.
Three weeks after nucleotomy disc height was reduced by 26%, and magnetic resonance imaging signal intensity by 40%. At 24 weeks disc height was decreased by 32%. Increased degenerative changes were found in a histodegeneration score 3 and 24 weeks after nucleotomy, as well as considerable NP scarification after 3 weeks. In controls, cytokeratin-8 immunohistochemistry identified NCs in proximity to chondrocyte-like NP cells at approximately equal ratio. After nucleotomy, NCs were considerably reduced to <10% of total NP cells. Matrix genes were upregulated, except for aggrecan that decreased to 35% of initial values 3 weeks after nucleotomy. Matrix degrading factors (matrix metalloproteinases 13 and 3) were continuously upregulated, whereas transcripts of their inhibitors (tissue inhibitors of matrix metalloproteinase 2 and 3) were downregulated. No significant changes in segmental spinal flexibility or bone density were found after nucleotomy.
We introduced a new disc degeneration model with relatively large discs that could be used for cell therapeutic approaches. The study gives further information about disc remodeling after nucleotomy and indicates the relevance of an altered cellular composition for the development of disc degeneration.</description><identifier>ISSN: 0362-2436</identifier><identifier>EISSN: 1528-1159</identifier><identifier>DOI: 10.1097/BRS.0b013e3181b723c9</identifier><identifier>PMID: 19940730</identifier><identifier>CODEN: SPINDD</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Aggrecans - metabolism ; Animals ; Biological and medical sciences ; Biomechanical Phenomena ; Cerebrospinal fluid. Meninges. Spinal cord ; Chondrocytes - metabolism ; Chondrocytes - pathology ; Development. Senescence. Regeneration. Transplantation ; Disease Models, Animal ; Diskectomy - methods ; Fundamental and applied biological sciences. Psychology ; Intervertebral Disc - metabolism ; Intervertebral Disc - pathology ; Intervertebral Disc - surgery ; Intervertebral Disc Degeneration - metabolism ; Intervertebral Disc Degeneration - pathology ; Intervertebral Disc Degeneration - surgery ; Keratin-8 - metabolism ; Magnetic Resonance Imaging ; Matrix Metalloproteinase 13 - metabolism ; Matrix Metalloproteinase 3 - metabolism ; Medical sciences ; Nervous system (semeiology, syndromes) ; Neurology ; Swine ; Swine, Miniature ; Tissue Inhibitor of Metalloproteinase-2 - metabolism ; Tissue Inhibitor of Metalloproteinase-3 - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Spine (Philadelphia, Pa. 1976), 2009-12, Vol.34 (25), p.2730-2739</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c314t-f4a3c2407748ca965b34f3081077a77ff6c1d6fc085be9d987bdbd52a3c019d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22208458$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19940730$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OMLOR, Georg W</creatorcontrib><creatorcontrib>NERLICH, Andreas G</creatorcontrib><creatorcontrib>WILKE, Hans-Joachim</creatorcontrib><creatorcontrib>PFEIFFER, Michael</creatorcontrib><creatorcontrib>LORENZ, Helga</creatorcontrib><creatorcontrib>SCHAAF-KEIM, Markus</creatorcontrib><creatorcontrib>BERTRAM, Helge</creatorcontrib><creatorcontrib>RICHTER, Wiltrud</creatorcontrib><creatorcontrib>CARSTENS, Claus</creatorcontrib><creatorcontrib>GUEHRING, Thorsten</creatorcontrib><title>A New Porcine In Vivo Animal Model of Disc Degeneration: Response of Anulus Fibrosus Cells, Chondrocyte-Like Nucleus Pulposus Cells, and Notochordal Nucleus Pulposus Cells to Partial Nucleotomy</title><title>Spine (Philadelphia, Pa. 1976)</title><addtitle>Spine (Phila Pa 1976)</addtitle><description>In vivo animal study.
To describe a new porcine disc degeneration model, and to analyze disc remodeling and degeneration after nucleotomy with special view to the different nucleus pulposus (NP) cell types.
Thus far, predominantly smaller animals were used for disc degeneration models; however, such small discs were inappropriate to investigate cell implementation therapies. Though notochordal cells (NCs) are important for disc formation and maintenance, differences in the amount of NCs between human and animal discs have often been neglected.
Twenty-four Goettingen minipigs underwent partial nucleotomy with a 16G biopsy cannula, to remove approximately 10% of total NP volume. Animals were followed up for 3, or 24 weeks and analyzed by radiographs, MRIs, (immuno)histology, gene expression analysis, and biomechanical testing.
Three weeks after nucleotomy disc height was reduced by 26%, and magnetic resonance imaging signal intensity by 40%. At 24 weeks disc height was decreased by 32%. Increased degenerative changes were found in a histodegeneration score 3 and 24 weeks after nucleotomy, as well as considerable NP scarification after 3 weeks. In controls, cytokeratin-8 immunohistochemistry identified NCs in proximity to chondrocyte-like NP cells at approximately equal ratio. After nucleotomy, NCs were considerably reduced to <10% of total NP cells. Matrix genes were upregulated, except for aggrecan that decreased to 35% of initial values 3 weeks after nucleotomy. Matrix degrading factors (matrix metalloproteinases 13 and 3) were continuously upregulated, whereas transcripts of their inhibitors (tissue inhibitors of matrix metalloproteinase 2 and 3) were downregulated. No significant changes in segmental spinal flexibility or bone density were found after nucleotomy.
We introduced a new disc degeneration model with relatively large discs that could be used for cell therapeutic approaches. The study gives further information about disc remodeling after nucleotomy and indicates the relevance of an altered cellular composition for the development of disc degeneration.</description><subject>Aggrecans - metabolism</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biomechanical Phenomena</subject><subject>Cerebrospinal fluid. Meninges. Spinal cord</subject><subject>Chondrocytes - metabolism</subject><subject>Chondrocytes - pathology</subject><subject>Development. Senescence. Regeneration. Transplantation</subject><subject>Disease Models, Animal</subject><subject>Diskectomy - methods</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Intervertebral Disc - metabolism</subject><subject>Intervertebral Disc - pathology</subject><subject>Intervertebral Disc - surgery</subject><subject>Intervertebral Disc Degeneration - metabolism</subject><subject>Intervertebral Disc Degeneration - pathology</subject><subject>Intervertebral Disc Degeneration - surgery</subject><subject>Keratin-8 - metabolism</subject><subject>Magnetic Resonance Imaging</subject><subject>Matrix Metalloproteinase 13 - metabolism</subject><subject>Matrix Metalloproteinase 3 - metabolism</subject><subject>Medical sciences</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neurology</subject><subject>Swine</subject><subject>Swine, Miniature</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - metabolism</subject><subject>Tissue Inhibitor of Metalloproteinase-3 - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0362-2436</issn><issn>1528-1159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkd1uEzEQhS0EomnhDRDyDeKm2_pvd23uQkqhUghR-bldee0xNWzs1N4tyuPxZrhqKAhxZcvzHc_MOQg9o-SEEtWevr78eEJ6QjlwKmnfMm7UAzSjNZMVpbV6iGaEN6xigjcH6DDnb4SQhlP1GB1QpQRpOZmhn3O8gh94HZPxAfBFwF_8TcTz4Dd6wO-jhQFHh898NvgMvkKApEcfwyt8CXkbQ4bb8jxMw5Txue9TzOWygGHIx3hxFYNN0exGqJb-O-DVZAYo9fU0bP8GdbB4FcdormKype__OTxGvNZp9L-JotjsnqBHTg8Znu7PI_T5_M2nxbtq-eHtxWK-rAynYqyc0NywsnUrpNGqqXsuHCeSlhfdts41htrGGSLrHpRVsu1tb2tWVIQqW_Mj9PLu322K1xPksdsUU8pcOkCcctdyQWspmCykuCNNcSMncN02FTvTrqOku82uK9l1_2ZXZM_3DaZ-A_aPaB9WAV7sAZ2NHlzSwfh8zzHGiBS15L8AZPulsw</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>OMLOR, Georg W</creator><creator>NERLICH, Andreas G</creator><creator>WILKE, Hans-Joachim</creator><creator>PFEIFFER, Michael</creator><creator>LORENZ, Helga</creator><creator>SCHAAF-KEIM, Markus</creator><creator>BERTRAM, Helge</creator><creator>RICHTER, Wiltrud</creator><creator>CARSTENS, Claus</creator><creator>GUEHRING, Thorsten</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20091201</creationdate><title>A New Porcine In Vivo Animal Model of Disc Degeneration: Response of Anulus Fibrosus Cells, Chondrocyte-Like Nucleus Pulposus Cells, and Notochordal Nucleus Pulposus Cells to Partial Nucleotomy</title><author>OMLOR, Georg W ; NERLICH, Andreas G ; WILKE, Hans-Joachim ; PFEIFFER, Michael ; LORENZ, Helga ; SCHAAF-KEIM, Markus ; BERTRAM, Helge ; RICHTER, Wiltrud ; CARSTENS, Claus ; GUEHRING, Thorsten</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c314t-f4a3c2407748ca965b34f3081077a77ff6c1d6fc085be9d987bdbd52a3c019d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aggrecans - metabolism</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biomechanical Phenomena</topic><topic>Cerebrospinal fluid. Meninges. Spinal cord</topic><topic>Chondrocytes - metabolism</topic><topic>Chondrocytes - pathology</topic><topic>Development. Senescence. Regeneration. Transplantation</topic><topic>Disease Models, Animal</topic><topic>Diskectomy - methods</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Intervertebral Disc - metabolism</topic><topic>Intervertebral Disc - pathology</topic><topic>Intervertebral Disc - surgery</topic><topic>Intervertebral Disc Degeneration - metabolism</topic><topic>Intervertebral Disc Degeneration - pathology</topic><topic>Intervertebral Disc Degeneration - surgery</topic><topic>Keratin-8 - metabolism</topic><topic>Magnetic Resonance Imaging</topic><topic>Matrix Metalloproteinase 13 - metabolism</topic><topic>Matrix Metalloproteinase 3 - metabolism</topic><topic>Medical sciences</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neurology</topic><topic>Swine</topic><topic>Swine, Miniature</topic><topic>Tissue Inhibitor of Metalloproteinase-2 - metabolism</topic><topic>Tissue Inhibitor of Metalloproteinase-3 - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OMLOR, Georg W</creatorcontrib><creatorcontrib>NERLICH, Andreas G</creatorcontrib><creatorcontrib>WILKE, Hans-Joachim</creatorcontrib><creatorcontrib>PFEIFFER, Michael</creatorcontrib><creatorcontrib>LORENZ, Helga</creatorcontrib><creatorcontrib>SCHAAF-KEIM, Markus</creatorcontrib><creatorcontrib>BERTRAM, Helge</creatorcontrib><creatorcontrib>RICHTER, Wiltrud</creatorcontrib><creatorcontrib>CARSTENS, Claus</creatorcontrib><creatorcontrib>GUEHRING, Thorsten</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Spine (Philadelphia, Pa. 1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OMLOR, Georg W</au><au>NERLICH, Andreas G</au><au>WILKE, Hans-Joachim</au><au>PFEIFFER, Michael</au><au>LORENZ, Helga</au><au>SCHAAF-KEIM, Markus</au><au>BERTRAM, Helge</au><au>RICHTER, Wiltrud</au><au>CARSTENS, Claus</au><au>GUEHRING, Thorsten</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A New Porcine In Vivo Animal Model of Disc Degeneration: Response of Anulus Fibrosus Cells, Chondrocyte-Like Nucleus Pulposus Cells, and Notochordal Nucleus Pulposus Cells to Partial Nucleotomy</atitle><jtitle>Spine (Philadelphia, Pa. 1976)</jtitle><addtitle>Spine (Phila Pa 1976)</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>34</volume><issue>25</issue><spage>2730</spage><epage>2739</epage><pages>2730-2739</pages><issn>0362-2436</issn><eissn>1528-1159</eissn><coden>SPINDD</coden><abstract>In vivo animal study.
To describe a new porcine disc degeneration model, and to analyze disc remodeling and degeneration after nucleotomy with special view to the different nucleus pulposus (NP) cell types.
Thus far, predominantly smaller animals were used for disc degeneration models; however, such small discs were inappropriate to investigate cell implementation therapies. Though notochordal cells (NCs) are important for disc formation and maintenance, differences in the amount of NCs between human and animal discs have often been neglected.
Twenty-four Goettingen minipigs underwent partial nucleotomy with a 16G biopsy cannula, to remove approximately 10% of total NP volume. Animals were followed up for 3, or 24 weeks and analyzed by radiographs, MRIs, (immuno)histology, gene expression analysis, and biomechanical testing.
Three weeks after nucleotomy disc height was reduced by 26%, and magnetic resonance imaging signal intensity by 40%. At 24 weeks disc height was decreased by 32%. Increased degenerative changes were found in a histodegeneration score 3 and 24 weeks after nucleotomy, as well as considerable NP scarification after 3 weeks. In controls, cytokeratin-8 immunohistochemistry identified NCs in proximity to chondrocyte-like NP cells at approximately equal ratio. After nucleotomy, NCs were considerably reduced to <10% of total NP cells. Matrix genes were upregulated, except for aggrecan that decreased to 35% of initial values 3 weeks after nucleotomy. Matrix degrading factors (matrix metalloproteinases 13 and 3) were continuously upregulated, whereas transcripts of their inhibitors (tissue inhibitors of matrix metalloproteinase 2 and 3) were downregulated. No significant changes in segmental spinal flexibility or bone density were found after nucleotomy.
We introduced a new disc degeneration model with relatively large discs that could be used for cell therapeutic approaches. The study gives further information about disc remodeling after nucleotomy and indicates the relevance of an altered cellular composition for the development of disc degeneration.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>19940730</pmid><doi>10.1097/BRS.0b013e3181b723c9</doi><tpages>10</tpages></addata></record> |
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subjects | Aggrecans - metabolism Animals Biological and medical sciences Biomechanical Phenomena Cerebrospinal fluid. Meninges. Spinal cord Chondrocytes - metabolism Chondrocytes - pathology Development. Senescence. Regeneration. Transplantation Disease Models, Animal Diskectomy - methods Fundamental and applied biological sciences. Psychology Intervertebral Disc - metabolism Intervertebral Disc - pathology Intervertebral Disc - surgery Intervertebral Disc Degeneration - metabolism Intervertebral Disc Degeneration - pathology Intervertebral Disc Degeneration - surgery Keratin-8 - metabolism Magnetic Resonance Imaging Matrix Metalloproteinase 13 - metabolism Matrix Metalloproteinase 3 - metabolism Medical sciences Nervous system (semeiology, syndromes) Neurology Swine Swine, Miniature Tissue Inhibitor of Metalloproteinase-2 - metabolism Tissue Inhibitor of Metalloproteinase-3 - metabolism Vertebrates: nervous system and sense organs |
title | A New Porcine In Vivo Animal Model of Disc Degeneration: Response of Anulus Fibrosus Cells, Chondrocyte-Like Nucleus Pulposus Cells, and Notochordal Nucleus Pulposus Cells to Partial Nucleotomy |
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