Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging
Perivascular fibroblasts (PVFs) are recognized for their pro-fibrotic role in many central nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. However, these shared attributes hinder the ability to distinguish PVFs from mural cells. We used in vivo two-photon...
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Veröffentlicht in: | Journal of cerebral blood flow and metabolism 2022-06, Vol.42 (6), p.966-978 |
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creator | Bonney, Stephanie K Sullivan, Liam T Cherry, Timothy J Daneman, Richard Shih, Andy Y |
description | Perivascular fibroblasts (PVFs) are recognized for their pro-fibrotic role in many central nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. However, these shared attributes hinder the ability to distinguish PVFs from mural cells. We used in vivo two-photon imaging and transgenic mice with PVF-targeting promoters (Col1a1 or Col1a2) to compare the structure and distribution of PVFs and mural cells in cerebral cortex of healthy, adult mice. We show that PVFs localize to all cortical penetrating arterioles and their offshoots (arteriole-capillary transition zone), as well as the main trunk of only larger ascending venules. However, the capillary zone is devoid of PVF coverage. PVFs display short-range mobility along the vessel wall and exhibit distinct structural features (flattened somata and thin ruffled processes) not seen with smooth muscle cells or pericytes. These findings clarify that PVFs and mural cells are distinct cell types coexisting in a similar perivascular niche. |
doi_str_mv | 10.1177/0271678X211068528 |
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Like mural cells, PVFs surround blood vessels and express Pdgfrβ. However, these shared attributes hinder the ability to distinguish PVFs from mural cells. We used in vivo two-photon imaging and transgenic mice with PVF-targeting promoters (Col1a1 or Col1a2) to compare the structure and distribution of PVFs and mural cells in cerebral cortex of healthy, adult mice. We show that PVFs localize to all cortical penetrating arterioles and their offshoots (arteriole-capillary transition zone), as well as the main trunk of only larger ascending venules. However, the capillary zone is devoid of PVF coverage. PVFs display short-range mobility along the vessel wall and exhibit distinct structural features (flattened somata and thin ruffled processes) not seen with smooth muscle cells or pericytes. These findings clarify that PVFs and mural cells are distinct cell types coexisting in a similar perivascular niche.</description><identifier>ISSN: 0271-678X</identifier><identifier>EISSN: 1559-7016</identifier><identifier>DOI: 10.1177/0271678X211068528</identifier><identifier>PMID: 34929105</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Animals ; Brain - blood supply ; Capillaries - diagnostic imaging ; Fibroblasts - metabolism ; Mice ; Mice, Transgenic ; Original ; Pericytes - metabolism</subject><ispartof>Journal of cerebral blood flow and metabolism, 2022-06, Vol.42 (6), p.966-978</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021 2021 International Society for Cerebral Blood Flow and Metabolism</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c486t-41bcab87bea02f7e298bfc1685519b0c9a92dc1990154c212126290e2d6bf8d53</citedby><cites>FETCH-LOGICAL-c486t-41bcab87bea02f7e298bfc1685519b0c9a92dc1990154c212126290e2d6bf8d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125487/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125487/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,21819,27924,27925,43621,43622,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34929105$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bonney, Stephanie K</creatorcontrib><creatorcontrib>Sullivan, Liam T</creatorcontrib><creatorcontrib>Cherry, Timothy J</creatorcontrib><creatorcontrib>Daneman, Richard</creatorcontrib><creatorcontrib>Shih, Andy Y</creatorcontrib><title>Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging</title><title>Journal of cerebral blood flow and metabolism</title><addtitle>J Cereb Blood Flow Metab</addtitle><description>Perivascular fibroblasts (PVFs) are recognized for their pro-fibrotic role in many central nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. However, these shared attributes hinder the ability to distinguish PVFs from mural cells. We used in vivo two-photon imaging and transgenic mice with PVF-targeting promoters (Col1a1 or Col1a2) to compare the structure and distribution of PVFs and mural cells in cerebral cortex of healthy, adult mice. We show that PVFs localize to all cortical penetrating arterioles and their offshoots (arteriole-capillary transition zone), as well as the main trunk of only larger ascending venules. However, the capillary zone is devoid of PVF coverage. PVFs display short-range mobility along the vessel wall and exhibit distinct structural features (flattened somata and thin ruffled processes) not seen with smooth muscle cells or pericytes. These findings clarify that PVFs and mural cells are distinct cell types coexisting in a similar perivascular niche.</description><subject>Animals</subject><subject>Brain - blood supply</subject><subject>Capillaries - diagnostic imaging</subject><subject>Fibroblasts - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Original</subject><subject>Pericytes - metabolism</subject><issn>0271-678X</issn><issn>1559-7016</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU9PHCEYxolpU1fbD-Cl4djLWF52YOBiYtT-SUy81MQbAYZZ2czCCswYv71s1pqaJoYDh_f3PDwvD0InQE4Buu47oR3wTtxRAMIFo-IALYAx2XQE-Ae02M2bHXCIjnJeE0LEkrFP6HDZSiqBsAVaX_pcfLAFD06XKbmM44BN0j7grUt-1tlOo0548CZFM-pcMtahx5sp6RFbN44ZJzc7PboemydcdbOfIy6PsdnexxID9hu98mH1GX0c9Jjdl5f7GN3-uPpz8au5vvn5--L8urGt4KVpwVhtRGecJnToHJXCDBbqfgykIVZqSXsLUhJgraVQD6eSONpzM4ieLY_R2d53O5mN660LpUZV21RzpCcVtVdvJ8Hfq1WclQTKWtFVg28vBik-TC4XtfF5t6kOLk5ZUQ50KSlveUVhj9oUc05ueH0GiNp1pP7rqGq-_pvvVfG3lAqc7oGsV06t45RC_a93HJ8B1VecgA</recordid><startdate>20220601</startdate><enddate>20220601</enddate><creator>Bonney, Stephanie K</creator><creator>Sullivan, Liam T</creator><creator>Cherry, Timothy J</creator><creator>Daneman, Richard</creator><creator>Shih, Andy Y</creator><general>SAGE Publications</general><scope>AFRWT</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><scope>5PM</scope></search><sort><creationdate>20220601</creationdate><title>Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging</title><author>Bonney, Stephanie K ; Sullivan, Liam T ; Cherry, Timothy J ; Daneman, Richard ; Shih, Andy Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c486t-41bcab87bea02f7e298bfc1685519b0c9a92dc1990154c212126290e2d6bf8d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Brain - blood supply</topic><topic>Capillaries - diagnostic imaging</topic><topic>Fibroblasts - metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Original</topic><topic>Pericytes - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bonney, Stephanie K</creatorcontrib><creatorcontrib>Sullivan, Liam T</creatorcontrib><creatorcontrib>Cherry, Timothy J</creatorcontrib><creatorcontrib>Daneman, Richard</creatorcontrib><creatorcontrib>Shih, Andy Y</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cerebral blood flow and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bonney, Stephanie K</au><au>Sullivan, Liam T</au><au>Cherry, Timothy J</au><au>Daneman, Richard</au><au>Shih, Andy Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging</atitle><jtitle>Journal of cerebral blood flow and metabolism</jtitle><addtitle>J Cereb Blood Flow Metab</addtitle><date>2022-06-01</date><risdate>2022</risdate><volume>42</volume><issue>6</issue><spage>966</spage><epage>978</epage><pages>966-978</pages><issn>0271-678X</issn><eissn>1559-7016</eissn><abstract>Perivascular fibroblasts (PVFs) are recognized for their pro-fibrotic role in many central nervous system disorders. Like mural cells, PVFs surround blood vessels and express Pdgfrβ. However, these shared attributes hinder the ability to distinguish PVFs from mural cells. We used in vivo two-photon imaging and transgenic mice with PVF-targeting promoters (Col1a1 or Col1a2) to compare the structure and distribution of PVFs and mural cells in cerebral cortex of healthy, adult mice. We show that PVFs localize to all cortical penetrating arterioles and their offshoots (arteriole-capillary transition zone), as well as the main trunk of only larger ascending venules. However, the capillary zone is devoid of PVF coverage. PVFs display short-range mobility along the vessel wall and exhibit distinct structural features (flattened somata and thin ruffled processes) not seen with smooth muscle cells or pericytes. These findings clarify that PVFs and mural cells are distinct cell types coexisting in a similar perivascular niche.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>34929105</pmid><doi>10.1177/0271678X211068528</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Brain - blood supply Capillaries - diagnostic imaging Fibroblasts - metabolism Mice Mice, Transgenic Original Pericytes - metabolism |
title | Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging |
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