The peridural membrane of the spine has characteristics of synovium
The peridural membrane (PDM) is a well‐defined structure between dura mater and the wall of the spinal canal. The spine may be viewed as a multi‐segmented joint, with the epidural cavity and neural foramina as joint spaces and PDM as synovial lining. The objective of this investigation was to determ...
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Veröffentlicht in: | Anatomical record (Hoboken, N.J. : 2007) N.J. : 2007), 2021-03, Vol.304 (3), p.631-646 |
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description | The peridural membrane (PDM) is a well‐defined structure between dura mater and the wall of the spinal canal. The spine may be viewed as a multi‐segmented joint, with the epidural cavity and neural foramina as joint spaces and PDM as synovial lining. The objective of this investigation was to determine if PDM has histological characteristics of synovium. Samples of the PDM of the thoraco‐lumbar spine were taken from 23 human cadavers and analyzed with conventional light microscopy and confocal microscopy. Results were compared to reports on similar analyses of synovium in the literature. Histological distribution of areolar, fibrous, and adipose connective tissue in PDM was similar to synovium. The PDM has an intima and sub‐intima. No basement membrane was identified. CD68, a marker for macrophage‐like‐synoviocytes, and CD55, a marker for fibroblast‐like synoviocytes, were seen in the lining and sub‐lining of the PDM. Multifunctional hyaluronan receptor CD44 and hyaluronic acid synthetase 2 marker HAS2 were abundantly present throughout the membrane. Marked presence of CD44, CD55, and HAS2 in the well‐developed tunica muscularis of blood vessels and in the body of the PDM suggests a role in the maintenance and lubrication of the epidural cavity and neural foramina. Presence of CD68, CD55, and CD44 suggests a scavenging function and a role in the inflammatory response to noxious stimuli. Thus, the human PDM has histological and immunohistochemical characteristics of synovium. This suggests that the PDM may be important for the homeostasis of the flexible spine and the neural structures it contains. |
doi_str_mv | 10.1002/ar.24474 |
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The spine may be viewed as a multi‐segmented joint, with the epidural cavity and neural foramina as joint spaces and PDM as synovial lining. The objective of this investigation was to determine if PDM has histological characteristics of synovium. Samples of the PDM of the thoraco‐lumbar spine were taken from 23 human cadavers and analyzed with conventional light microscopy and confocal microscopy. Results were compared to reports on similar analyses of synovium in the literature. Histological distribution of areolar, fibrous, and adipose connective tissue in PDM was similar to synovium. The PDM has an intima and sub‐intima. No basement membrane was identified. CD68, a marker for macrophage‐like‐synoviocytes, and CD55, a marker for fibroblast‐like synoviocytes, were seen in the lining and sub‐lining of the PDM. Multifunctional hyaluronan receptor CD44 and hyaluronic acid synthetase 2 marker HAS2 were abundantly present throughout the membrane. Marked presence of CD44, CD55, and HAS2 in the well‐developed tunica muscularis of blood vessels and in the body of the PDM suggests a role in the maintenance and lubrication of the epidural cavity and neural foramina. Presence of CD68, CD55, and CD44 suggests a scavenging function and a role in the inflammatory response to noxious stimuli. Thus, the human PDM has histological and immunohistochemical characteristics of synovium. 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The spine may be viewed as a multi‐segmented joint, with the epidural cavity and neural foramina as joint spaces and PDM as synovial lining. The objective of this investigation was to determine if PDM has histological characteristics of synovium. Samples of the PDM of the thoraco‐lumbar spine were taken from 23 human cadavers and analyzed with conventional light microscopy and confocal microscopy. Results were compared to reports on similar analyses of synovium in the literature. Histological distribution of areolar, fibrous, and adipose connective tissue in PDM was similar to synovium. The PDM has an intima and sub‐intima. No basement membrane was identified. CD68, a marker for macrophage‐like‐synoviocytes, and CD55, a marker for fibroblast‐like synoviocytes, were seen in the lining and sub‐lining of the PDM. Multifunctional hyaluronan receptor CD44 and hyaluronic acid synthetase 2 marker HAS2 were abundantly present throughout the membrane. Marked presence of CD44, CD55, and HAS2 in the well‐developed tunica muscularis of blood vessels and in the body of the PDM suggests a role in the maintenance and lubrication of the epidural cavity and neural foramina. Presence of CD68, CD55, and CD44 suggests a scavenging function and a role in the inflammatory response to noxious stimuli. Thus, the human PDM has histological and immunohistochemical characteristics of synovium. This suggests that the PDM may be important for the homeostasis of the flexible spine and the neural structures it contains.</description><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, Myelomonocytic - metabolism</subject><subject>Blood vessels</subject><subject>Cadavers</subject><subject>CD44 antigen</subject><subject>CD55 Antigens - metabolism</subject><subject>Confocal microscopy</subject><subject>Connective tissues</subject><subject>Dura mater</subject><subject>Epidural</subject><subject>Epidural Space - metabolism</subject><subject>Female</subject><subject>histology</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Hyaluronan Receptors - metabolism</subject><subject>Hyaluronic acid</subject><subject>immunohistochemistry</subject><subject>Inflammation</subject><subject>Light microscopy</subject><subject>Macrophages</subject><subject>Male</subject><subject>Microscopy</subject><subject>Middle Aged</subject><subject>Pain perception</subject><subject>peridural membrane</subject><subject>spine</subject><subject>Spine (lumbar)</subject><subject>Spine - metabolism</subject><subject>Synovial Membrane - metabolism</subject><subject>Synoviocytes</subject><subject>Synovium</subject><issn>1932-8486</issn><issn>1932-8494</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF1LwzAUhoMobk7BXyAFb7zpzMdJm1yO4RcMBJnXIUlT1tGuNWmV_XszNxUEr04O5-HhzYvQJcFTgjG91X5KAXI4QmMiGU0FSDj-eYtshM5CWGPMAUt2ikaMcpYLzsdovly5pHO-Kgav66RxjfF645K2TPp4CV0Vl5UOiV1pr20fydBXNuyAsN2079XQnKOTUtfBXRzmBL3e3y3nj-ni-eFpPluklgkGaQaQxQhEkMLQQmbGFlBqLZjh1DjKpLCOC2viSRtb5nmZYSAZl1gay7KCTdDN3tv59m1woVdNFayr6xi4HYKiQABjCQwiev0HXbeD38R0kRISx-9z_iu0vg3Bu1J1vmq03yqC1a5Ypb36KjaiVwfhYBpX_IDfTUYg3QMfVe22_4rU7GUv_AS65H-k</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>Bosscher, Hemmo A.</creator><creator>Grozdanov, Petar N.</creator><creator>Warraich, Irfan I.</creator><creator>MacDonald, Clinton C.</creator><creator>Day, Miles R.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1852-5150</orcidid></search><sort><creationdate>202103</creationdate><title>The peridural membrane of the spine has characteristics of synovium</title><author>Bosscher, Hemmo A. ; Grozdanov, Petar N. ; Warraich, Irfan I. ; MacDonald, Clinton C. ; Day, Miles R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3834-6446005181db2d96bcd4faa83b52be2398ce58cbd96abcf77f604165909bc36d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, Myelomonocytic - metabolism</topic><topic>Blood vessels</topic><topic>Cadavers</topic><topic>CD44 antigen</topic><topic>CD55 Antigens - metabolism</topic><topic>Confocal microscopy</topic><topic>Connective tissues</topic><topic>Dura mater</topic><topic>Epidural</topic><topic>Epidural Space - metabolism</topic><topic>Female</topic><topic>histology</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Hyaluronan Receptors - metabolism</topic><topic>Hyaluronic acid</topic><topic>immunohistochemistry</topic><topic>Inflammation</topic><topic>Light microscopy</topic><topic>Macrophages</topic><topic>Male</topic><topic>Microscopy</topic><topic>Middle Aged</topic><topic>Pain perception</topic><topic>peridural membrane</topic><topic>spine</topic><topic>Spine (lumbar)</topic><topic>Spine - metabolism</topic><topic>Synovial Membrane - metabolism</topic><topic>Synoviocytes</topic><topic>Synovium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bosscher, Hemmo A.</creatorcontrib><creatorcontrib>Grozdanov, Petar N.</creatorcontrib><creatorcontrib>Warraich, Irfan I.</creatorcontrib><creatorcontrib>MacDonald, Clinton C.</creatorcontrib><creatorcontrib>Day, Miles R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bosscher, Hemmo A.</au><au>Grozdanov, Petar N.</au><au>Warraich, Irfan I.</au><au>MacDonald, Clinton C.</au><au>Day, Miles R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The peridural membrane of the spine has characteristics of synovium</atitle><jtitle>Anatomical record (Hoboken, N.J. : 2007)</jtitle><addtitle>Anat Rec (Hoboken)</addtitle><date>2021-03</date><risdate>2021</risdate><volume>304</volume><issue>3</issue><spage>631</spage><epage>646</epage><pages>631-646</pages><issn>1932-8486</issn><eissn>1932-8494</eissn><abstract>The peridural membrane (PDM) is a well‐defined structure between dura mater and the wall of the spinal canal. The spine may be viewed as a multi‐segmented joint, with the epidural cavity and neural foramina as joint spaces and PDM as synovial lining. The objective of this investigation was to determine if PDM has histological characteristics of synovium. Samples of the PDM of the thoraco‐lumbar spine were taken from 23 human cadavers and analyzed with conventional light microscopy and confocal microscopy. Results were compared to reports on similar analyses of synovium in the literature. Histological distribution of areolar, fibrous, and adipose connective tissue in PDM was similar to synovium. The PDM has an intima and sub‐intima. No basement membrane was identified. CD68, a marker for macrophage‐like‐synoviocytes, and CD55, a marker for fibroblast‐like synoviocytes, were seen in the lining and sub‐lining of the PDM. Multifunctional hyaluronan receptor CD44 and hyaluronic acid synthetase 2 marker HAS2 were abundantly present throughout the membrane. Marked presence of CD44, CD55, and HAS2 in the well‐developed tunica muscularis of blood vessels and in the body of the PDM suggests a role in the maintenance and lubrication of the epidural cavity and neural foramina. Presence of CD68, CD55, and CD44 suggests a scavenging function and a role in the inflammatory response to noxious stimuli. Thus, the human PDM has histological and immunohistochemical characteristics of synovium. This suggests that the PDM may be important for the homeostasis of the flexible spine and the neural structures it contains.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32537855</pmid><doi>10.1002/ar.24474</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0002-1852-5150</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Blood vessels Cadavers CD44 antigen CD55 Antigens - metabolism Confocal microscopy Connective tissues Dura mater Epidural Epidural Space - metabolism Female histology Homeostasis Humans Hyaluronan Receptors - metabolism Hyaluronic acid immunohistochemistry Inflammation Light microscopy Macrophages Male Microscopy Middle Aged Pain perception peridural membrane spine Spine (lumbar) Spine - metabolism Synovial Membrane - metabolism Synoviocytes Synovium |
title | The peridural membrane of the spine has characteristics of synovium |
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