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- Publisher Website: 10.1369/jhc.2008.952184
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- PMID: 19001641
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Conference Paper: Matrix remodeling during intervertebral disc growth and degeneration detected by multichromatic fast staining
Title | Matrix remodeling during intervertebral disc growth and degeneration detected by multichromatic fast staining | ||||||
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Authors | |||||||
Keywords | Degeneration Growth Intervertebral disc Matrix Remodeling Staining and labeling | ||||||
Issue Date | 2009 | ||||||
Publisher | Histochemical Society. The Journal's web site is located at http://intl.jhc.org | ||||||
Citation | The 55th Annual Meeting of the Orthopaedic Research Society (ORS 2009), Las Vegas, NV., 22-24 February 2009. In Journal of Histochemistry and Cytochemistry, 2009, v. 57 n. 3, p. 249-256 How to Cite? | ||||||
Abstract | Various imaging techniques have been used to assess degeneration of the intervertebral disc, including many histological methods, but cartilage-oriented histological stains do not clearly show the comparatively complex structures of the disc. In addition, there is no integrated method to assess efficiently both the compartmental organization and matrix composition in disc samples. In this study, a novel histological method, termed FAST staining, has been developed to investigate disc growth and degeneration by sequen- tial staining with fast green, Alcian blue, Safranin-O, and tartrazine to generate multi- chromatic histological profiles (FAST profiles). This identifies the major compartments of the vertebra-disc region, including the cartilaginous endplate and multiple zones of the annulus fibrosus, by specific FAST profile patterns. A disc degeneration model in rabbit established using a previously described puncture method showed gradual but profound alteration of the FAST profile during disc degeneration, supporting continual alteration of glycosaminoglycan. Changes of the FAST profile pattern in the nucleus pulposus and an- nulus fibrosus of the postnatal mouse spine suggested matrix remodeling activity during the growth of intervertebral discs. In summary, we developed an effective staining method capable of defining intervertebral disc compartments in detail and showing matrix remodel- ing events within the disc. The FAST staining method may be used to develop a histopatho- logical grading system to evaluate disc degeneration or malformation. © The Histochemical Society, Inc. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/61626 | ||||||
ISSN | 2023 Impact Factor: 1.9 2023 SCImago Journal Rankings: 1.177 | ||||||
PubMed Central ID | |||||||
ISI Accession Number ID |
Funding Information: We thank Prof. Koichi Masuda and his team in Rush Medical Center, Chicago, IL, for excellent technical advice on the generation of rabbit disc degeneration model. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Leung, VYL | en_HK |
dc.contributor.author | Chan, WCW | en_HK |
dc.contributor.author | Hung, SC | en_HK |
dc.contributor.author | Cheung, KMC | en_HK |
dc.contributor.author | Chan, D | en_HK |
dc.date.accessioned | 2010-07-13T03:43:45Z | - |
dc.date.available | 2010-07-13T03:43:45Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | The 55th Annual Meeting of the Orthopaedic Research Society (ORS 2009), Las Vegas, NV., 22-24 February 2009. In Journal of Histochemistry and Cytochemistry, 2009, v. 57 n. 3, p. 249-256 | - |
dc.identifier.issn | 0022-1554 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/61626 | - |
dc.description.abstract | Various imaging techniques have been used to assess degeneration of the intervertebral disc, including many histological methods, but cartilage-oriented histological stains do not clearly show the comparatively complex structures of the disc. In addition, there is no integrated method to assess efficiently both the compartmental organization and matrix composition in disc samples. In this study, a novel histological method, termed FAST staining, has been developed to investigate disc growth and degeneration by sequen- tial staining with fast green, Alcian blue, Safranin-O, and tartrazine to generate multi- chromatic histological profiles (FAST profiles). This identifies the major compartments of the vertebra-disc region, including the cartilaginous endplate and multiple zones of the annulus fibrosus, by specific FAST profile patterns. A disc degeneration model in rabbit established using a previously described puncture method showed gradual but profound alteration of the FAST profile during disc degeneration, supporting continual alteration of glycosaminoglycan. Changes of the FAST profile pattern in the nucleus pulposus and an- nulus fibrosus of the postnatal mouse spine suggested matrix remodeling activity during the growth of intervertebral discs. In summary, we developed an effective staining method capable of defining intervertebral disc compartments in detail and showing matrix remodel- ing events within the disc. The FAST staining method may be used to develop a histopatho- logical grading system to evaluate disc degeneration or malformation. © The Histochemical Society, Inc. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Histochemical Society. The Journal's web site is located at http://intl.jhc.org | en_HK |
dc.relation.ispartof | Journal of Histochemistry and Cytochemistry | en_HK |
dc.subject | Degeneration | en_HK |
dc.subject | Growth | en_HK |
dc.subject | Intervertebral disc | en_HK |
dc.subject | Matrix | en_HK |
dc.subject | Remodeling | en_HK |
dc.subject | Staining and labeling | en_HK |
dc.subject.mesh | Extracellular Matrix - pathology | - |
dc.subject.mesh | Intervertebral Disc - growth and development - pathology | - |
dc.subject.mesh | Phenazines | - |
dc.subject.mesh | Spinal Diseases - pathology | - |
dc.subject.mesh | Tartrazine | - |
dc.title | Matrix remodeling during intervertebral disc growth and degeneration detected by multichromatic fast staining | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.email | Leung, VYL: vicleung@hku.hk | en_HK |
dc.identifier.email | Cheung, KMC: cheungmc@hku.hk | en_HK |
dc.identifier.email | Chan, D: chand@hkucc.hku.hk | en_HK |
dc.identifier.authority | Leung, VYL=rp01764 | en_HK |
dc.identifier.authority | Cheung, KMC=rp00387 | en_HK |
dc.identifier.authority | Chan, D=rp00540 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1369/jhc.2008.952184 | en_HK |
dc.identifier.pmid | 19001641 | - |
dc.identifier.pmcid | PMC2664937 | - |
dc.identifier.scopus | eid_2-s2.0-62649088064 | en_HK |
dc.identifier.hkuros | 160667 | en_HK |
dc.identifier.hkuros | 160660 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-62649088064&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 57 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 249 | en_HK |
dc.identifier.epage | 256 | en_HK |
dc.identifier.isi | WOS:000263530800007 | - |
dc.publisher.place | United States | en_HK |
dc.description.other | The 55th Annual Meeting of the Orthopaedic Research Society, Las Vegas, NV., 22-24 February 2009. In Journal of Histochemistry and Cytochemistry, 2009, v. 57 n. 3, p. 249-256 | - |
dc.identifier.scopusauthorid | Leung, VYL=35337438900 | en_HK |
dc.identifier.scopusauthorid | Chan, WCW=24545687600 | en_HK |
dc.identifier.scopusauthorid | Hung, SC=35757582000 | en_HK |
dc.identifier.scopusauthorid | Cheung, KMC=7402406754 | en_HK |
dc.identifier.scopusauthorid | Chan, D=7402216545 | en_HK |
dc.customcontrol.immutable | sml 170106 amended | - |
dc.identifier.issnl | 0022-1554 | - |