Neurons express hemoglobin α- and β-chains in rat and human brains
Hemoglobin is the oxygen carrier in vertebrate blood erythrocytes. Here we report that hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin. Transcriptome analyses of laser‐capture microdissected nigral dopaminergic neurons in rats and striatal neuron...
Gespeichert in:
Veröffentlicht in: | Journal of comparative neurology (1911) 2009-08, Vol.515 (5), p.538-547 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 547 |
---|---|
container_issue | 5 |
container_start_page | 538 |
container_title | Journal of comparative neurology (1911) |
container_volume | 515 |
creator | Richter, Franziska Meurers, Bernhard H. Zhu, Chunni Medvedeva, Vera P. Chesselet, Marie-Françoise |
description | Hemoglobin is the oxygen carrier in vertebrate blood erythrocytes. Here we report that hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin. Transcriptome analyses of laser‐capture microdissected nigral dopaminergic neurons in rats and striatal neurons in mice revealed the presence of hemoglobin α, adult chain 2 (Hba‐a2) and hemoglobin β (Hbb) transcripts, whereas other erythroid markers were not detected. Quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) analysis confirmed the expression of Hba‐a2 and Hbb in nigral dopaminergic neurons, striatal γ‐aminobutyric acid (GABA)ergic neurons, and cortical pyramidal neurons in rats. Combined in situ hybridization histochemistry and immunohistochemistry with the neuronal marker neuronal nuclear antigen (NeuN) in rat brain further confirmed the presence of hemoglobin mRNAs in neurons. Immunohistochemistry identified hemoglobin α‐ and β‐chains in both rat and human brains, and hemoglobin proteins were detected by Western blotting in whole rat brain tissue as well as in cultures of mesencephalic neurons, further excluding the possibility of blood contamination. Systemic administration of the mitochondrial inhibitor rotenone (2 mg/kg/d, 7d, s.c.) induced a marked decrease in Hba‐a2 and Hbb but not neuroglobin or cytoglobin mRNA in transcriptome analyses of nigral dopaminergic neurons. Quantitative RT‐PCR confirmed the transcriptional downregulation of Hba‐a2 and Hbb in nigral, striatal, and cortical neurons. Thus, hemoglobin chains are expressed in neurons and are regulated by treatments that affect mitochondria, opening up the possibility that they may play a novel role in neuronal function and response to injury. J. Comp. Neurol. 515:538–547, 2009. © 2009 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cne.22062 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3123135</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67374426</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4512-11d288a74b8365f8de94a4fad4834f76f61d875d9e5a364de46f4796514570cc3</originalsourceid><addsrcrecordid>eNp1kMtOwzAQRS0EgvJY8AMoKyQWaf2KE2-QUCkFhAoLoIiN5SYTGsij2A20nwUfwjdh2lJgwWqkO2fuXF2EdgluEoxpKy6hSSkWdAU1CJbCl5Egq6jhdsSXUoQbaNPaR4yxlCxaRxtE8lBKSRvouAe1qUrrwWRkwFpvCEX1kFeDrPQ-3nxPl4n38e7HQ505yIlGj2fisC506Q3Ml76N1lKdW9hZzC10c9K5bp_6F5fds_bRhR_zgFCfkIRGkQ75IGIiSKMEJNc81QmPGE9DkQqSRGGQSAg0EzwBLlKXUwSEByGOY7aFDue-o3pQQBJDOTY6VyOTFdpMVaUz9XdTZkP1UL0oRigjLHAG-wsDUz3XYMeqyGwMea5LqGqrRMhCzqlw4MEcjE1lrYF0-YRg9dW5cp2rWeeO3fud6odclOyA1hx4zXKY_u-k2r3Ot6U_v8jsGCbLC22eZhED1e91Vf_8jt1fdam6ZZ9TbJvJ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67374426</pqid></control><display><type>article</type><title>Neurons express hemoglobin α- and β-chains in rat and human brains</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Richter, Franziska ; Meurers, Bernhard H. ; Zhu, Chunni ; Medvedeva, Vera P. ; Chesselet, Marie-Françoise</creator><creatorcontrib>Richter, Franziska ; Meurers, Bernhard H. ; Zhu, Chunni ; Medvedeva, Vera P. ; Chesselet, Marie-Françoise</creatorcontrib><description>Hemoglobin is the oxygen carrier in vertebrate blood erythrocytes. Here we report that hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin. Transcriptome analyses of laser‐capture microdissected nigral dopaminergic neurons in rats and striatal neurons in mice revealed the presence of hemoglobin α, adult chain 2 (Hba‐a2) and hemoglobin β (Hbb) transcripts, whereas other erythroid markers were not detected. Quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) analysis confirmed the expression of Hba‐a2 and Hbb in nigral dopaminergic neurons, striatal γ‐aminobutyric acid (GABA)ergic neurons, and cortical pyramidal neurons in rats. Combined in situ hybridization histochemistry and immunohistochemistry with the neuronal marker neuronal nuclear antigen (NeuN) in rat brain further confirmed the presence of hemoglobin mRNAs in neurons. Immunohistochemistry identified hemoglobin α‐ and β‐chains in both rat and human brains, and hemoglobin proteins were detected by Western blotting in whole rat brain tissue as well as in cultures of mesencephalic neurons, further excluding the possibility of blood contamination. Systemic administration of the mitochondrial inhibitor rotenone (2 mg/kg/d, 7d, s.c.) induced a marked decrease in Hba‐a2 and Hbb but not neuroglobin or cytoglobin mRNA in transcriptome analyses of nigral dopaminergic neurons. Quantitative RT‐PCR confirmed the transcriptional downregulation of Hba‐a2 and Hbb in nigral, striatal, and cortical neurons. Thus, hemoglobin chains are expressed in neurons and are regulated by treatments that affect mitochondria, opening up the possibility that they may play a novel role in neuronal function and response to injury. J. Comp. Neurol. 515:538–547, 2009. © 2009 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.22062</identifier><identifier>PMID: 19479992</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Animals ; Gene Expression Profiling ; hemoglobin ; Hemoglobin A2 - genetics ; Hemoglobin A2 - metabolism ; Hemoglobins - genetics ; Hemoglobins - metabolism ; Humans ; Immunohistochemistry ; In Situ Hybridization ; in vivo ; laser-capture microdissection ; Male ; Mice ; Mitochondria - drug effects ; Mitochondria - metabolism ; neuronal expression ; Neurons - cytology ; Neurons - metabolism ; Rats ; Rats, Inbred Lew ; rotenone ; Rotenone - pharmacology ; rotenone, in vivo ; transcriptome analysis ; Uncoupling Agents - pharmacology</subject><ispartof>Journal of comparative neurology (1911), 2009-08, Vol.515 (5), p.538-547</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>Copyright 2009 Wiley-Liss, Inc.</rights><rights>2009 Wiley-Liss, Inc. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4512-11d288a74b8365f8de94a4fad4834f76f61d875d9e5a364de46f4796514570cc3</citedby><cites>FETCH-LOGICAL-c4512-11d288a74b8365f8de94a4fad4834f76f61d875d9e5a364de46f4796514570cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcne.22062$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.22062$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19479992$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Richter, Franziska</creatorcontrib><creatorcontrib>Meurers, Bernhard H.</creatorcontrib><creatorcontrib>Zhu, Chunni</creatorcontrib><creatorcontrib>Medvedeva, Vera P.</creatorcontrib><creatorcontrib>Chesselet, Marie-Françoise</creatorcontrib><title>Neurons express hemoglobin α- and β-chains in rat and human brains</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Hemoglobin is the oxygen carrier in vertebrate blood erythrocytes. Here we report that hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin. Transcriptome analyses of laser‐capture microdissected nigral dopaminergic neurons in rats and striatal neurons in mice revealed the presence of hemoglobin α, adult chain 2 (Hba‐a2) and hemoglobin β (Hbb) transcripts, whereas other erythroid markers were not detected. Quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) analysis confirmed the expression of Hba‐a2 and Hbb in nigral dopaminergic neurons, striatal γ‐aminobutyric acid (GABA)ergic neurons, and cortical pyramidal neurons in rats. Combined in situ hybridization histochemistry and immunohistochemistry with the neuronal marker neuronal nuclear antigen (NeuN) in rat brain further confirmed the presence of hemoglobin mRNAs in neurons. Immunohistochemistry identified hemoglobin α‐ and β‐chains in both rat and human brains, and hemoglobin proteins were detected by Western blotting in whole rat brain tissue as well as in cultures of mesencephalic neurons, further excluding the possibility of blood contamination. Systemic administration of the mitochondrial inhibitor rotenone (2 mg/kg/d, 7d, s.c.) induced a marked decrease in Hba‐a2 and Hbb but not neuroglobin or cytoglobin mRNA in transcriptome analyses of nigral dopaminergic neurons. Quantitative RT‐PCR confirmed the transcriptional downregulation of Hba‐a2 and Hbb in nigral, striatal, and cortical neurons. Thus, hemoglobin chains are expressed in neurons and are regulated by treatments that affect mitochondria, opening up the possibility that they may play a novel role in neuronal function and response to injury. J. Comp. Neurol. 515:538–547, 2009. © 2009 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Animals</subject><subject>Gene Expression Profiling</subject><subject>hemoglobin</subject><subject>Hemoglobin A2 - genetics</subject><subject>Hemoglobin A2 - metabolism</subject><subject>Hemoglobins - genetics</subject><subject>Hemoglobins - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization</subject><subject>in vivo</subject><subject>laser-capture microdissection</subject><subject>Male</subject><subject>Mice</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>neuronal expression</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>rotenone</subject><subject>Rotenone - pharmacology</subject><subject>rotenone, in vivo</subject><subject>transcriptome analysis</subject><subject>Uncoupling Agents - pharmacology</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRS0EgvJY8AMoKyQWaf2KE2-QUCkFhAoLoIiN5SYTGsij2A20nwUfwjdh2lJgwWqkO2fuXF2EdgluEoxpKy6hSSkWdAU1CJbCl5Egq6jhdsSXUoQbaNPaR4yxlCxaRxtE8lBKSRvouAe1qUrrwWRkwFpvCEX1kFeDrPQ-3nxPl4n38e7HQ505yIlGj2fisC506Q3Ml76N1lKdW9hZzC10c9K5bp_6F5fds_bRhR_zgFCfkIRGkQ75IGIiSKMEJNc81QmPGE9DkQqSRGGQSAg0EzwBLlKXUwSEByGOY7aFDue-o3pQQBJDOTY6VyOTFdpMVaUz9XdTZkP1UL0oRigjLHAG-wsDUz3XYMeqyGwMea5LqGqrRMhCzqlw4MEcjE1lrYF0-YRg9dW5cp2rWeeO3fud6odclOyA1hx4zXKY_u-k2r3Ot6U_v8jsGCbLC22eZhED1e91Vf_8jt1fdam6ZZ9TbJvJ</recordid><startdate>20090810</startdate><enddate>20090810</enddate><creator>Richter, Franziska</creator><creator>Meurers, Bernhard H.</creator><creator>Zhu, Chunni</creator><creator>Medvedeva, Vera P.</creator><creator>Chesselet, Marie-Françoise</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>20090810</creationdate><title>Neurons express hemoglobin α- and β-chains in rat and human brains</title><author>Richter, Franziska ; Meurers, Bernhard H. ; Zhu, Chunni ; Medvedeva, Vera P. ; Chesselet, Marie-Françoise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4512-11d288a74b8365f8de94a4fad4834f76f61d875d9e5a364de46f4796514570cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Animals</topic><topic>Gene Expression Profiling</topic><topic>hemoglobin</topic><topic>Hemoglobin A2 - genetics</topic><topic>Hemoglobin A2 - metabolism</topic><topic>Hemoglobins - genetics</topic><topic>Hemoglobins - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization</topic><topic>in vivo</topic><topic>laser-capture microdissection</topic><topic>Male</topic><topic>Mice</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>neuronal expression</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>rotenone</topic><topic>Rotenone - pharmacology</topic><topic>rotenone, in vivo</topic><topic>transcriptome analysis</topic><topic>Uncoupling Agents - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Richter, Franziska</creatorcontrib><creatorcontrib>Meurers, Bernhard H.</creatorcontrib><creatorcontrib>Zhu, Chunni</creatorcontrib><creatorcontrib>Medvedeva, Vera P.</creatorcontrib><creatorcontrib>Chesselet, Marie-Françoise</creatorcontrib><collection>Istex</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 comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Richter, Franziska</au><au>Meurers, Bernhard H.</au><au>Zhu, Chunni</au><au>Medvedeva, Vera P.</au><au>Chesselet, Marie-Françoise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurons express hemoglobin α- and β-chains in rat and human brains</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2009-08-10</date><risdate>2009</risdate><volume>515</volume><issue>5</issue><spage>538</spage><epage>547</epage><pages>538-547</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Hemoglobin is the oxygen carrier in vertebrate blood erythrocytes. Here we report that hemoglobin chains are expressed in mammalian brain neurons and are regulated by a mitochondrial toxin. Transcriptome analyses of laser‐capture microdissected nigral dopaminergic neurons in rats and striatal neurons in mice revealed the presence of hemoglobin α, adult chain 2 (Hba‐a2) and hemoglobin β (Hbb) transcripts, whereas other erythroid markers were not detected. Quantitative reverse transcriptase‐polymerase chain reaction (RT‐PCR) analysis confirmed the expression of Hba‐a2 and Hbb in nigral dopaminergic neurons, striatal γ‐aminobutyric acid (GABA)ergic neurons, and cortical pyramidal neurons in rats. Combined in situ hybridization histochemistry and immunohistochemistry with the neuronal marker neuronal nuclear antigen (NeuN) in rat brain further confirmed the presence of hemoglobin mRNAs in neurons. Immunohistochemistry identified hemoglobin α‐ and β‐chains in both rat and human brains, and hemoglobin proteins were detected by Western blotting in whole rat brain tissue as well as in cultures of mesencephalic neurons, further excluding the possibility of blood contamination. Systemic administration of the mitochondrial inhibitor rotenone (2 mg/kg/d, 7d, s.c.) induced a marked decrease in Hba‐a2 and Hbb but not neuroglobin or cytoglobin mRNA in transcriptome analyses of nigral dopaminergic neurons. Quantitative RT‐PCR confirmed the transcriptional downregulation of Hba‐a2 and Hbb in nigral, striatal, and cortical neurons. Thus, hemoglobin chains are expressed in neurons and are regulated by treatments that affect mitochondria, opening up the possibility that they may play a novel role in neuronal function and response to injury. J. Comp. Neurol. 515:538–547, 2009. © 2009 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19479992</pmid><doi>10.1002/cne.22062</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9967 |
ispartof | Journal of comparative neurology (1911), 2009-08, Vol.515 (5), p.538-547 |
issn | 0021-9967 1096-9861 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3123135 |
source | MEDLINE; Wiley Online Library All Journals |
subjects | Adult Animals Gene Expression Profiling hemoglobin Hemoglobin A2 - genetics Hemoglobin A2 - metabolism Hemoglobins - genetics Hemoglobins - metabolism Humans Immunohistochemistry In Situ Hybridization in vivo laser-capture microdissection Male Mice Mitochondria - drug effects Mitochondria - metabolism neuronal expression Neurons - cytology Neurons - metabolism Rats Rats, Inbred Lew rotenone Rotenone - pharmacology rotenone, in vivo transcriptome analysis Uncoupling Agents - pharmacology |
title | Neurons express hemoglobin α- and β-chains in rat and human brains |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T10%3A32%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Neurons%20express%20hemoglobin%20%CE%B1-%20and%20%CE%B2-chains%20in%20rat%20and%20human%20brains&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Richter,%20Franziska&rft.date=2009-08-10&rft.volume=515&rft.issue=5&rft.spage=538&rft.epage=547&rft.pages=538-547&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.22062&rft_dat=%3Cproquest_pubme%3E67374426%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67374426&rft_id=info:pmid/19479992&rfr_iscdi=true |