Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia

The effects of two bone morphogenetic proteins (BMP6, BMP7), alone and in combination with neurotrophins, were tested on cultures of embryonic day 15 rat septum. A week‐long exposure to BMP6 or BMP7 in the optimal concentration range of 2–5 n m increased the activity of choline acetyltransferase (Ch...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurochemistry 2001-04, Vol.77 (2), p.691-699
Hauptverfasser: Nonner, Doris, Barrett, Ellen F., Kaplan, Paul, Barrett, John N.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 699
container_issue 2
container_start_page 691
container_title Journal of neurochemistry
container_volume 77
creator Nonner, Doris
Barrett, Ellen F.
Kaplan, Paul
Barrett, John N.
description The effects of two bone morphogenetic proteins (BMP6, BMP7), alone and in combination with neurotrophins, were tested on cultures of embryonic day 15 rat septum. A week‐long exposure to BMP6 or BMP7 in the optimal concentration range of 2–5 n m increased the activity of choline acetyltransferase (ChAT) by 1.6–2‐fold, in both septal and combined septal−hippocampal cultures. The increase in ChAT activity reached significance after 4 days and continued to increase over an 11‐day exposure. Under control culture conditions neither BMP significantly altered the number of cholinergic neurons, and BMP effects on ChAT activity were less than linearly additive with those of nerve growth factor. The effects of BMPs and BMP + neurotrophin combinations were also assayed under two stress conditions: low‐density culture and hypoglycemia. In low‐density cultures BMPs and BMP + neurotrophin combinations preserved ChAT activity more effectively than neurotrophins alone. During 24 h hypoglycemic stress, BMPs alone did not preserve ChAT activity, but BMP + neurotrophin combinations preserved ChAT activity much more effectively than neurotrophins alone. These results demonstrate that BMP6 and BMP7 enhance ChAT activity under control and low‐density stress conditions, and that during a hypoglycemic stress their trophic effect requires and complements that exerted by neurotrophins.
doi_str_mv 10.1046/j.1471-4159.2001.00273.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_18080606</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>18080606</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4913-e711f4395314e168235e2035ea49ae6169646be115f6aa43163af01e0878305d3</originalsourceid><addsrcrecordid>eNqNkcuO1DAQRS0EYnoGfgF5gRCzSHDFjpMsWDAtnhoeC1hbHqfScSuxg53A9IfwvzjTLWDJxi6VT_mq7iWEAsuBCflin4OoIBNQNnnBGOSMFRXPb--RzZ-H-2STukXGmSjOyHmM-wRKIeEhOQMomoZz2JBfV94hHX2Yer9Dh7M1dAp-RusifX718Yuk2rU0FdUlRddrZ5DOPR4hM9sfSLHrUkV9Rx0uqR381K_j3lGzDPMSsKURp1kP1PR-sA7DLsncwQlrl2DdjvaHye-Gg8HR6kfkQaeHiI9P9wX59ub11-277Prz2_fbV9eZEQ3wDCuATvCm5CAQZF3wEguWDi0ajRJkk_a9QYCyk1oLDpLrjgGyuqo5K1t-QZ4d_03bfF8wzmq00eAwaId-iQpqVjPJZALrI2iCjzFgp6ZgRx0OCphaI1F7tTqvVufVGom6i0TdptEnJ43lZsT27-ApgwQ8PQE6Gj10IXls4z8ClaihSdjLI_bTDnj4b3314dN2rfhvwq6oAA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18080606</pqid></control><display><type>article</type><title>Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia</title><source>Wiley-Blackwell Journals</source><source>MEDLINE</source><source>Wiley Online Library Free Content</source><source>IngentaConnect Open Access Journals</source><source>Free E-Journal (出版社公開部分のみ)</source><source>Free Full-Text Journals in Chemistry</source><creator>Nonner, Doris ; Barrett, Ellen F. ; Kaplan, Paul ; Barrett, John N.</creator><creatorcontrib>Nonner, Doris ; Barrett, Ellen F. ; Kaplan, Paul ; Barrett, John N.</creatorcontrib><description>The effects of two bone morphogenetic proteins (BMP6, BMP7), alone and in combination with neurotrophins, were tested on cultures of embryonic day 15 rat septum. A week‐long exposure to BMP6 or BMP7 in the optimal concentration range of 2–5 n m increased the activity of choline acetyltransferase (ChAT) by 1.6–2‐fold, in both septal and combined septal−hippocampal cultures. The increase in ChAT activity reached significance after 4 days and continued to increase over an 11‐day exposure. Under control culture conditions neither BMP significantly altered the number of cholinergic neurons, and BMP effects on ChAT activity were less than linearly additive with those of nerve growth factor. The effects of BMPs and BMP + neurotrophin combinations were also assayed under two stress conditions: low‐density culture and hypoglycemia. In low‐density cultures BMPs and BMP + neurotrophin combinations preserved ChAT activity more effectively than neurotrophins alone. During 24 h hypoglycemic stress, BMPs alone did not preserve ChAT activity, but BMP + neurotrophin combinations preserved ChAT activity much more effectively than neurotrophins alone. These results demonstrate that BMP6 and BMP7 enhance ChAT activity under control and low‐density stress conditions, and that during a hypoglycemic stress their trophic effect requires and complements that exerted by neurotrophins.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.2001.00273.x</identifier><identifier>PMID: 11299331</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; Biochemistry and metabolism ; Biological and medical sciences ; Bone Morphogenetic Protein 6 ; Bone Morphogenetic Protein 7 ; bone morphogenetic proteins ; Bone Morphogenetic Proteins - pharmacology ; Brain-Derived Neurotrophic Factor - pharmacology ; Cells, Cultured ; Central nervous system ; choline acetyltransferase ; Choline O-Acetyltransferase - biosynthesis ; Drug Synergism ; Fundamental and applied biological sciences. Psychology ; Hippocampus - cytology ; Hippocampus - embryology ; hypoglycemia ; Hypoglycemia - metabolism ; Nerve Growth Factor - pharmacology ; Nerve Growth Factors - pharmacology ; Nerve Tissue Proteins - biosynthesis ; Neurons - drug effects ; Neurons - metabolism ; Neuroprotective Agents - pharmacology ; Neurotrophin 3 - pharmacology ; neurotrophins ; Rats ; Rats, Sprague-Dawley ; septal cholinergic neurons ; Septum Pellucidum - cytology ; Septum Pellucidum - embryology ; stress protection ; Stress, Physiological - metabolism ; Transforming Growth Factor beta ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 2001-04, Vol.77 (2), p.691-699</ispartof><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4913-e711f4395314e168235e2035ea49ae6169646be115f6aa43163af01e0878305d3</citedby><cites>FETCH-LOGICAL-c4913-e711f4395314e168235e2035ea49ae6169646be115f6aa43163af01e0878305d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1471-4159.2001.00273.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1471-4159.2001.00273.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1074819$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11299331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nonner, Doris</creatorcontrib><creatorcontrib>Barrett, Ellen F.</creatorcontrib><creatorcontrib>Kaplan, Paul</creatorcontrib><creatorcontrib>Barrett, John N.</creatorcontrib><title>Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>The effects of two bone morphogenetic proteins (BMP6, BMP7), alone and in combination with neurotrophins, were tested on cultures of embryonic day 15 rat septum. A week‐long exposure to BMP6 or BMP7 in the optimal concentration range of 2–5 n m increased the activity of choline acetyltransferase (ChAT) by 1.6–2‐fold, in both septal and combined septal−hippocampal cultures. The increase in ChAT activity reached significance after 4 days and continued to increase over an 11‐day exposure. Under control culture conditions neither BMP significantly altered the number of cholinergic neurons, and BMP effects on ChAT activity were less than linearly additive with those of nerve growth factor. The effects of BMPs and BMP + neurotrophin combinations were also assayed under two stress conditions: low‐density culture and hypoglycemia. In low‐density cultures BMPs and BMP + neurotrophin combinations preserved ChAT activity more effectively than neurotrophins alone. During 24 h hypoglycemic stress, BMPs alone did not preserve ChAT activity, but BMP + neurotrophin combinations preserved ChAT activity much more effectively than neurotrophins alone. These results demonstrate that BMP6 and BMP7 enhance ChAT activity under control and low‐density stress conditions, and that during a hypoglycemic stress their trophic effect requires and complements that exerted by neurotrophins.</description><subject>Animals</subject><subject>Biochemistry and metabolism</subject><subject>Biological and medical sciences</subject><subject>Bone Morphogenetic Protein 6</subject><subject>Bone Morphogenetic Protein 7</subject><subject>bone morphogenetic proteins</subject><subject>Bone Morphogenetic Proteins - pharmacology</subject><subject>Brain-Derived Neurotrophic Factor - pharmacology</subject><subject>Cells, Cultured</subject><subject>Central nervous system</subject><subject>choline acetyltransferase</subject><subject>Choline O-Acetyltransferase - biosynthesis</subject><subject>Drug Synergism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - embryology</subject><subject>hypoglycemia</subject><subject>Hypoglycemia - metabolism</subject><subject>Nerve Growth Factor - pharmacology</subject><subject>Nerve Growth Factors - pharmacology</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neurotrophin 3 - pharmacology</subject><subject>neurotrophins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>septal cholinergic neurons</subject><subject>Septum Pellucidum - cytology</subject><subject>Septum Pellucidum - embryology</subject><subject>stress protection</subject><subject>Stress, Physiological - metabolism</subject><subject>Transforming Growth Factor beta</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcuO1DAQRS0EYnoGfgF5gRCzSHDFjpMsWDAtnhoeC1hbHqfScSuxg53A9IfwvzjTLWDJxi6VT_mq7iWEAsuBCflin4OoIBNQNnnBGOSMFRXPb--RzZ-H-2STukXGmSjOyHmM-wRKIeEhOQMomoZz2JBfV94hHX2Yer9Dh7M1dAp-RusifX718Yuk2rU0FdUlRddrZ5DOPR4hM9sfSLHrUkV9Rx0uqR381K_j3lGzDPMSsKURp1kP1PR-sA7DLsncwQlrl2DdjvaHye-Gg8HR6kfkQaeHiI9P9wX59ub11-277Prz2_fbV9eZEQ3wDCuATvCm5CAQZF3wEguWDi0ajRJkk_a9QYCyk1oLDpLrjgGyuqo5K1t-QZ4d_03bfF8wzmq00eAwaId-iQpqVjPJZALrI2iCjzFgp6ZgRx0OCphaI1F7tTqvVufVGom6i0TdptEnJ43lZsT27-ApgwQ8PQE6Gj10IXls4z8ClaihSdjLI_bTDnj4b3314dN2rfhvwq6oAA</recordid><startdate>200104</startdate><enddate>200104</enddate><creator>Nonner, Doris</creator><creator>Barrett, Ellen F.</creator><creator>Kaplan, Paul</creator><creator>Barrett, John N.</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><scope>IQODW</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>7TK</scope></search><sort><creationdate>200104</creationdate><title>Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia</title><author>Nonner, Doris ; Barrett, Ellen F. ; Kaplan, Paul ; Barrett, John N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4913-e711f4395314e168235e2035ea49ae6169646be115f6aa43163af01e0878305d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Biochemistry and metabolism</topic><topic>Biological and medical sciences</topic><topic>Bone Morphogenetic Protein 6</topic><topic>Bone Morphogenetic Protein 7</topic><topic>bone morphogenetic proteins</topic><topic>Bone Morphogenetic Proteins - pharmacology</topic><topic>Brain-Derived Neurotrophic Factor - pharmacology</topic><topic>Cells, Cultured</topic><topic>Central nervous system</topic><topic>choline acetyltransferase</topic><topic>Choline O-Acetyltransferase - biosynthesis</topic><topic>Drug Synergism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hippocampus - cytology</topic><topic>Hippocampus - embryology</topic><topic>hypoglycemia</topic><topic>Hypoglycemia - metabolism</topic><topic>Nerve Growth Factor - pharmacology</topic><topic>Nerve Growth Factors - pharmacology</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Neurotrophin 3 - pharmacology</topic><topic>neurotrophins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>septal cholinergic neurons</topic><topic>Septum Pellucidum - cytology</topic><topic>Septum Pellucidum - embryology</topic><topic>stress protection</topic><topic>Stress, Physiological - metabolism</topic><topic>Transforming Growth Factor beta</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nonner, Doris</creatorcontrib><creatorcontrib>Barrett, Ellen F.</creatorcontrib><creatorcontrib>Kaplan, Paul</creatorcontrib><creatorcontrib>Barrett, John N.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nonner, Doris</au><au>Barrett, Ellen F.</au><au>Kaplan, Paul</au><au>Barrett, John N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2001-04</date><risdate>2001</risdate><volume>77</volume><issue>2</issue><spage>691</spage><epage>699</epage><pages>691-699</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>The effects of two bone morphogenetic proteins (BMP6, BMP7), alone and in combination with neurotrophins, were tested on cultures of embryonic day 15 rat septum. A week‐long exposure to BMP6 or BMP7 in the optimal concentration range of 2–5 n m increased the activity of choline acetyltransferase (ChAT) by 1.6–2‐fold, in both septal and combined septal−hippocampal cultures. The increase in ChAT activity reached significance after 4 days and continued to increase over an 11‐day exposure. Under control culture conditions neither BMP significantly altered the number of cholinergic neurons, and BMP effects on ChAT activity were less than linearly additive with those of nerve growth factor. The effects of BMPs and BMP + neurotrophin combinations were also assayed under two stress conditions: low‐density culture and hypoglycemia. In low‐density cultures BMPs and BMP + neurotrophin combinations preserved ChAT activity more effectively than neurotrophins alone. During 24 h hypoglycemic stress, BMPs alone did not preserve ChAT activity, but BMP + neurotrophin combinations preserved ChAT activity much more effectively than neurotrophins alone. These results demonstrate that BMP6 and BMP7 enhance ChAT activity under control and low‐density stress conditions, and that during a hypoglycemic stress their trophic effect requires and complements that exerted by neurotrophins.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11299331</pmid><doi>10.1046/j.1471-4159.2001.00273.x</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0022-3042
ispartof Journal of neurochemistry, 2001-04, Vol.77 (2), p.691-699
issn 0022-3042
1471-4159
language eng
recordid cdi_proquest_miscellaneous_18080606
source Wiley-Blackwell Journals; MEDLINE; Wiley Online Library Free Content; IngentaConnect Open Access Journals; Free E-Journal (出版社公開部分のみ); Free Full-Text Journals in Chemistry
subjects Animals
Biochemistry and metabolism
Biological and medical sciences
Bone Morphogenetic Protein 6
Bone Morphogenetic Protein 7
bone morphogenetic proteins
Bone Morphogenetic Proteins - pharmacology
Brain-Derived Neurotrophic Factor - pharmacology
Cells, Cultured
Central nervous system
choline acetyltransferase
Choline O-Acetyltransferase - biosynthesis
Drug Synergism
Fundamental and applied biological sciences. Psychology
Hippocampus - cytology
Hippocampus - embryology
hypoglycemia
Hypoglycemia - metabolism
Nerve Growth Factor - pharmacology
Nerve Growth Factors - pharmacology
Nerve Tissue Proteins - biosynthesis
Neurons - drug effects
Neurons - metabolism
Neuroprotective Agents - pharmacology
Neurotrophin 3 - pharmacology
neurotrophins
Rats
Rats, Sprague-Dawley
septal cholinergic neurons
Septum Pellucidum - cytology
Septum Pellucidum - embryology
stress protection
Stress, Physiological - metabolism
Transforming Growth Factor beta
Vertebrates: nervous system and sense organs
title Bone morphogenetic proteins (BMP6 and BMP7) enhance the protective effect of neurotrophins on cultured septal cholinergic neurons during hypoglycemia
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T08%3A31%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bone%20morphogenetic%20proteins%20(BMP6%20and%20BMP7)%20enhance%20the%20protective%20effect%20of%20neurotrophins%20on%20cultured%20septal%20cholinergic%20neurons%20during%20hypoglycemia&rft.jtitle=Journal%20of%20neurochemistry&rft.au=Nonner,%20Doris&rft.date=2001-04&rft.volume=77&rft.issue=2&rft.spage=691&rft.epage=699&rft.pages=691-699&rft.issn=0022-3042&rft.eissn=1471-4159&rft.coden=JONRA9&rft_id=info:doi/10.1046/j.1471-4159.2001.00273.x&rft_dat=%3Cproquest_cross%3E18080606%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18080606&rft_id=info:pmid/11299331&rfr_iscdi=true