Oligodendrocyte Slc48a1 (Hrg1) encodes a functional heme transporter required for myelin integrity
Oligodendrocytes (OLs) of the central nervous system require iron for proteolipid biosynthesis during the myelination process. Although most heme is found complexed to hemoglobin in red blood cells, surprisingly, we found that Slc48a1, encoding the heme transporter Hrg1, is expressed at higher level...
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Veröffentlicht in: | Glia 2025-02, Vol.73 (2), p.399-421 |
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creator | Stockley, John H. Vaquie, Adrien M. Xu, Zhaoyang Bartels, Theresa Jordan, Gregory D. Holmqvist, Staffan Gunter, Simon Lam, Guy Yamamoto, Daniel Pek, Rini H. Chambers, Ian G. Rock, Andrew S. Hill, Myfanwy Zhao, Chao Dillon, Scott Franklin, Robin J. M. O'Connor, Rosemary Bodine, David M. Hamza, Iqbal Rowitch, David H. |
description | Oligodendrocytes (OLs) of the central nervous system require iron for proteolipid biosynthesis during the myelination process. Although most heme is found complexed to hemoglobin in red blood cells, surprisingly, we found that Slc48a1, encoding the heme transporter Hrg1, is expressed at higher levels in OLs than any other cell type in rodent and humans. We confirmed in situ that Hrg1 is expressed in OLs but not their precursors (OPCs) and found that Hrg1 proteins in CNS white matter co‐localized within myelin sheaths. In older Hrg1 null mutant mice we observed reduced expression of myelin associated glycoprotein (Mag) and ultrastructural myelin defects reminiscent of Mag‐null animals, suggesting myelin adhesion deficiency. Further, we confirmed reduced myelin iron levels in Hrg1 null animals in vivo, and show that OLs in vitro can directly import both the fluorescent heme analogue ZnMP and heme itself, which rescued iron deficiency induced inhibition of OL differentiation in a heme‐oxidase‐dependent manner. Together these findings indicate OL Hrg1 encodes a functional heme transporter required for myelin integrity.
Main Points
Hrg1 is a heme transporter in myelin.
Heme is an auxiliary source of iron for oligodendrocytes and required for Mag expression.
Hrg1 KO mice have increased periaxonal space due to decreased levels of Mag. |
doi_str_mv | 10.1002/glia.24641 |
format | Article |
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Main Points
Hrg1 is a heme transporter in myelin.
Heme is an auxiliary source of iron for oligodendrocytes and required for Mag expression.
Hrg1 KO mice have increased periaxonal space due to decreased levels of Mag.</description><identifier>ISSN: 0894-1491</identifier><identifier>ISSN: 1098-1136</identifier><identifier>EISSN: 1098-1136</identifier><identifier>DOI: 10.1002/glia.24641</identifier><identifier>PMID: 39501820</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animals ; axon ; Biosynthesis ; Cells, Cultured ; Central nervous system ; Erythrocytes ; Fluorescence ; Glial stem cells ; Glycoproteins ; Heme ; Heme - metabolism ; heme oxygenase ; Hemoglobin ; Hrg1 ; Humans ; Integrity ; Iron ; Iron - metabolism ; Iron deficiency ; Membrane Transport Proteins - genetics ; Membrane Transport Proteins - metabolism ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Myelin ; myelin associated glycoprotein (Mag) ; myelin basic protein (Mbp) ; Myelin Sheath - metabolism ; Myelin-associated glycoprotein ; Myelin-Associated Glycoprotein - genetics ; Myelin-Associated Glycoprotein - metabolism ; Myelination ; neurodegeneration ; Nutrient deficiency ; oligodendrocyte ; Oligodendrocytes ; Oligodendroglia - metabolism ; Rats ; Sheaths ; Substantia alba</subject><ispartof>Glia, 2025-02, Vol.73 (2), p.399-421</ispartof><rights>2024 The Author(s). published by Wiley Periodicals LLC.</rights><rights>2024 The Author(s). GLIA published by Wiley Periodicals LLC.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3381-39104e07974f954006bb7556153f31fc48f167e59f3d135071c08c68e4bc1c3b3</cites><orcidid>0000-0002-7385-8310 ; 0000-0002-0079-0060 ; 0000-0003-4167-6456 ; 0000-0001-6522-2104</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fglia.24641$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fglia.24641$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39501820$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stockley, John H.</creatorcontrib><creatorcontrib>Vaquie, Adrien M.</creatorcontrib><creatorcontrib>Xu, Zhaoyang</creatorcontrib><creatorcontrib>Bartels, Theresa</creatorcontrib><creatorcontrib>Jordan, Gregory D.</creatorcontrib><creatorcontrib>Holmqvist, Staffan</creatorcontrib><creatorcontrib>Gunter, Simon</creatorcontrib><creatorcontrib>Lam, Guy</creatorcontrib><creatorcontrib>Yamamoto, Daniel</creatorcontrib><creatorcontrib>Pek, Rini H.</creatorcontrib><creatorcontrib>Chambers, Ian G.</creatorcontrib><creatorcontrib>Rock, Andrew S.</creatorcontrib><creatorcontrib>Hill, Myfanwy</creatorcontrib><creatorcontrib>Zhao, Chao</creatorcontrib><creatorcontrib>Dillon, Scott</creatorcontrib><creatorcontrib>Franklin, Robin J. M.</creatorcontrib><creatorcontrib>O'Connor, Rosemary</creatorcontrib><creatorcontrib>Bodine, David M.</creatorcontrib><creatorcontrib>Hamza, Iqbal</creatorcontrib><creatorcontrib>Rowitch, David H.</creatorcontrib><title>Oligodendrocyte Slc48a1 (Hrg1) encodes a functional heme transporter required for myelin integrity</title><title>Glia</title><addtitle>Glia</addtitle><description>Oligodendrocytes (OLs) of the central nervous system require iron for proteolipid biosynthesis during the myelination process. Although most heme is found complexed to hemoglobin in red blood cells, surprisingly, we found that Slc48a1, encoding the heme transporter Hrg1, is expressed at higher levels in OLs than any other cell type in rodent and humans. We confirmed in situ that Hrg1 is expressed in OLs but not their precursors (OPCs) and found that Hrg1 proteins in CNS white matter co‐localized within myelin sheaths. In older Hrg1 null mutant mice we observed reduced expression of myelin associated glycoprotein (Mag) and ultrastructural myelin defects reminiscent of Mag‐null animals, suggesting myelin adhesion deficiency. Further, we confirmed reduced myelin iron levels in Hrg1 null animals in vivo, and show that OLs in vitro can directly import both the fluorescent heme analogue ZnMP and heme itself, which rescued iron deficiency induced inhibition of OL differentiation in a heme‐oxidase‐dependent manner. Together these findings indicate OL Hrg1 encodes a functional heme transporter required for myelin integrity.
Main Points
Hrg1 is a heme transporter in myelin.
Heme is an auxiliary source of iron for oligodendrocytes and required for Mag expression.
Hrg1 KO mice have increased periaxonal space due to decreased levels of Mag.</description><subject>Animals</subject><subject>axon</subject><subject>Biosynthesis</subject><subject>Cells, Cultured</subject><subject>Central nervous system</subject><subject>Erythrocytes</subject><subject>Fluorescence</subject><subject>Glial stem cells</subject><subject>Glycoproteins</subject><subject>Heme</subject><subject>Heme - metabolism</subject><subject>heme oxygenase</subject><subject>Hemoglobin</subject><subject>Hrg1</subject><subject>Humans</subject><subject>Integrity</subject><subject>Iron</subject><subject>Iron - metabolism</subject><subject>Iron deficiency</subject><subject>Membrane Transport Proteins - genetics</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Myelin</subject><subject>myelin associated glycoprotein (Mag)</subject><subject>myelin basic protein (Mbp)</subject><subject>Myelin Sheath - metabolism</subject><subject>Myelin-associated glycoprotein</subject><subject>Myelin-Associated Glycoprotein - genetics</subject><subject>Myelin-Associated Glycoprotein - metabolism</subject><subject>Myelination</subject><subject>neurodegeneration</subject><subject>Nutrient deficiency</subject><subject>oligodendrocyte</subject><subject>Oligodendrocytes</subject><subject>Oligodendroglia - metabolism</subject><subject>Rats</subject><subject>Sheaths</subject><subject>Substantia alba</subject><issn>0894-1491</issn><issn>1098-1136</issn><issn>1098-1136</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi0Eokvhwg9AlrgUpBRP7DjxCVUV_ZBW6gE4W4kzSV059tZOQPn3eNm2Ag6cRqN59OjVvIS8BXYKjJWfRmfb01JIAc_IBphqCgAun5MNa5QoQCg4Iq9SumMM8lK_JEdcVQyakm1Id-PsGHr0fQxmnZF-dUY0LdCTqzjCB4re5GuiLR0Wb2YbfOvoLU5I59j6tAtxxkgj3i82Yk-HEOm0orOeWj_jGO28viYvhtYlfPMwj8n3iy_fzq-K7c3l9fnZtjCcN1BwBUwgq1UtBlUJxmTX1VUloeIDhyGnGkDWWKmB98ArVoNhjZENis6A4R0_Jp8P3t3STdgb9Dmi07topzauOrRW_33x9laP4YcGkLJUjcyGkwdDDPcLpllPNhl0rvUYlqQ55C8rgAoy-v4f9C4sMT9nT4laNoKrMlMfD5SJIaWIw1MaYHrfnd53p393l-F3f-Z_Qh_LygAcgJ_W4foflb7cXp8dpL8AUW-jlQ</recordid><startdate>202502</startdate><enddate>202502</enddate><creator>Stockley, John H.</creator><creator>Vaquie, Adrien M.</creator><creator>Xu, Zhaoyang</creator><creator>Bartels, Theresa</creator><creator>Jordan, Gregory D.</creator><creator>Holmqvist, Staffan</creator><creator>Gunter, Simon</creator><creator>Lam, Guy</creator><creator>Yamamoto, Daniel</creator><creator>Pek, Rini H.</creator><creator>Chambers, Ian G.</creator><creator>Rock, Andrew S.</creator><creator>Hill, Myfanwy</creator><creator>Zhao, Chao</creator><creator>Dillon, Scott</creator><creator>Franklin, Robin J. M.</creator><creator>O'Connor, Rosemary</creator><creator>Bodine, David M.</creator><creator>Hamza, Iqbal</creator><creator>Rowitch, David H.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</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>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7385-8310</orcidid><orcidid>https://orcid.org/0000-0002-0079-0060</orcidid><orcidid>https://orcid.org/0000-0003-4167-6456</orcidid><orcidid>https://orcid.org/0000-0001-6522-2104</orcidid></search><sort><creationdate>202502</creationdate><title>Oligodendrocyte Slc48a1 (Hrg1) encodes a functional heme transporter required for myelin integrity</title><author>Stockley, John H. ; Vaquie, Adrien M. ; Xu, Zhaoyang ; Bartels, Theresa ; Jordan, Gregory D. ; Holmqvist, Staffan ; Gunter, Simon ; Lam, Guy ; Yamamoto, Daniel ; Pek, Rini H. ; Chambers, Ian G. ; Rock, Andrew S. ; Hill, Myfanwy ; Zhao, Chao ; Dillon, Scott ; Franklin, Robin J. M. ; O'Connor, Rosemary ; Bodine, David M. ; Hamza, Iqbal ; Rowitch, David H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3381-39104e07974f954006bb7556153f31fc48f167e59f3d135071c08c68e4bc1c3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Animals</topic><topic>axon</topic><topic>Biosynthesis</topic><topic>Cells, Cultured</topic><topic>Central nervous system</topic><topic>Erythrocytes</topic><topic>Fluorescence</topic><topic>Glial stem cells</topic><topic>Glycoproteins</topic><topic>Heme</topic><topic>Heme - metabolism</topic><topic>heme oxygenase</topic><topic>Hemoglobin</topic><topic>Hrg1</topic><topic>Humans</topic><topic>Integrity</topic><topic>Iron</topic><topic>Iron - metabolism</topic><topic>Iron deficiency</topic><topic>Membrane Transport Proteins - genetics</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Myelin</topic><topic>myelin associated glycoprotein (Mag)</topic><topic>myelin basic protein (Mbp)</topic><topic>Myelin Sheath - metabolism</topic><topic>Myelin-associated glycoprotein</topic><topic>Myelin-Associated Glycoprotein - genetics</topic><topic>Myelin-Associated Glycoprotein - metabolism</topic><topic>Myelination</topic><topic>neurodegeneration</topic><topic>Nutrient deficiency</topic><topic>oligodendrocyte</topic><topic>Oligodendrocytes</topic><topic>Oligodendroglia - metabolism</topic><topic>Rats</topic><topic>Sheaths</topic><topic>Substantia alba</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stockley, John H.</creatorcontrib><creatorcontrib>Vaquie, Adrien M.</creatorcontrib><creatorcontrib>Xu, Zhaoyang</creatorcontrib><creatorcontrib>Bartels, Theresa</creatorcontrib><creatorcontrib>Jordan, Gregory D.</creatorcontrib><creatorcontrib>Holmqvist, Staffan</creatorcontrib><creatorcontrib>Gunter, Simon</creatorcontrib><creatorcontrib>Lam, Guy</creatorcontrib><creatorcontrib>Yamamoto, Daniel</creatorcontrib><creatorcontrib>Pek, Rini H.</creatorcontrib><creatorcontrib>Chambers, Ian G.</creatorcontrib><creatorcontrib>Rock, Andrew S.</creatorcontrib><creatorcontrib>Hill, Myfanwy</creatorcontrib><creatorcontrib>Zhao, Chao</creatorcontrib><creatorcontrib>Dillon, Scott</creatorcontrib><creatorcontrib>Franklin, Robin J. M.</creatorcontrib><creatorcontrib>O'Connor, Rosemary</creatorcontrib><creatorcontrib>Bodine, David M.</creatorcontrib><creatorcontrib>Hamza, Iqbal</creatorcontrib><creatorcontrib>Rowitch, David H.</creatorcontrib><collection>Wiley-Blackwell Open Access Titles(OpenAccess)</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Glia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stockley, John H.</au><au>Vaquie, Adrien M.</au><au>Xu, Zhaoyang</au><au>Bartels, Theresa</au><au>Jordan, Gregory D.</au><au>Holmqvist, Staffan</au><au>Gunter, Simon</au><au>Lam, Guy</au><au>Yamamoto, Daniel</au><au>Pek, Rini H.</au><au>Chambers, Ian G.</au><au>Rock, Andrew S.</au><au>Hill, Myfanwy</au><au>Zhao, Chao</au><au>Dillon, Scott</au><au>Franklin, Robin J. M.</au><au>O'Connor, Rosemary</au><au>Bodine, David M.</au><au>Hamza, Iqbal</au><au>Rowitch, David H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oligodendrocyte Slc48a1 (Hrg1) encodes a functional heme transporter required for myelin integrity</atitle><jtitle>Glia</jtitle><addtitle>Glia</addtitle><date>2025-02</date><risdate>2025</risdate><volume>73</volume><issue>2</issue><spage>399</spage><epage>421</epage><pages>399-421</pages><issn>0894-1491</issn><issn>1098-1136</issn><eissn>1098-1136</eissn><abstract>Oligodendrocytes (OLs) of the central nervous system require iron for proteolipid biosynthesis during the myelination process. Although most heme is found complexed to hemoglobin in red blood cells, surprisingly, we found that Slc48a1, encoding the heme transporter Hrg1, is expressed at higher levels in OLs than any other cell type in rodent and humans. We confirmed in situ that Hrg1 is expressed in OLs but not their precursors (OPCs) and found that Hrg1 proteins in CNS white matter co‐localized within myelin sheaths. In older Hrg1 null mutant mice we observed reduced expression of myelin associated glycoprotein (Mag) and ultrastructural myelin defects reminiscent of Mag‐null animals, suggesting myelin adhesion deficiency. Further, we confirmed reduced myelin iron levels in Hrg1 null animals in vivo, and show that OLs in vitro can directly import both the fluorescent heme analogue ZnMP and heme itself, which rescued iron deficiency induced inhibition of OL differentiation in a heme‐oxidase‐dependent manner. Together these findings indicate OL Hrg1 encodes a functional heme transporter required for myelin integrity.
Main Points
Hrg1 is a heme transporter in myelin.
Heme is an auxiliary source of iron for oligodendrocytes and required for Mag expression.
Hrg1 KO mice have increased periaxonal space due to decreased levels of Mag.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>39501820</pmid><doi>10.1002/glia.24641</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0002-7385-8310</orcidid><orcidid>https://orcid.org/0000-0002-0079-0060</orcidid><orcidid>https://orcid.org/0000-0003-4167-6456</orcidid><orcidid>https://orcid.org/0000-0001-6522-2104</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals axon Biosynthesis Cells, Cultured Central nervous system Erythrocytes Fluorescence Glial stem cells Glycoproteins Heme Heme - metabolism heme oxygenase Hemoglobin Hrg1 Humans Integrity Iron Iron - metabolism Iron deficiency Membrane Transport Proteins - genetics Membrane Transport Proteins - metabolism Mice Mice, Inbred C57BL Mice, Knockout Myelin myelin associated glycoprotein (Mag) myelin basic protein (Mbp) Myelin Sheath - metabolism Myelin-associated glycoprotein Myelin-Associated Glycoprotein - genetics Myelin-Associated Glycoprotein - metabolism Myelination neurodegeneration Nutrient deficiency oligodendrocyte Oligodendrocytes Oligodendroglia - metabolism Rats Sheaths Substantia alba |
title | Oligodendrocyte Slc48a1 (Hrg1) encodes a functional heme transporter required for myelin integrity |
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