Synergistic Induction of Pituitary Adenylate Cyclase‐Activating Polypeptide (PACAP) Gene Expression by Nerve Growth Factor and PACAP in PC12 Cells

: Pituitary adenylate cyclase‐activating polypeptide (PACAP) gene expression was analyzed in PC12 cells. PC12 cells transfected with a PACAP promoter‐luciferase reporter construct were utilized to investigate the effects of PACAP, either alone or in combination with nerve growth factor (NGF), on PAC...

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Veröffentlicht in:Journal of neurochemistry 2000-02, Vol.74 (2), p.501-507
Hauptverfasser: Hashimoto, Hitoshi, Hagihara, Nami, Koga, Kazumi, Yamamoto, Kyohei, Shintani, Norihito, Tomimoto, Shuhei, Mori, Wakaba, Koyama, Yutaka, Matsuda, Toshio, Baba, Akemichi
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container_title Journal of neurochemistry
container_volume 74
creator Hashimoto, Hitoshi
Hagihara, Nami
Koga, Kazumi
Yamamoto, Kyohei
Shintani, Norihito
Tomimoto, Shuhei
Mori, Wakaba
Koyama, Yutaka
Matsuda, Toshio
Baba, Akemichi
description : Pituitary adenylate cyclase‐activating polypeptide (PACAP) gene expression was analyzed in PC12 cells. PC12 cells transfected with a PACAP promoter‐luciferase reporter construct were utilized to investigate the effects of PACAP, either alone or in combination with nerve growth factor (NGF), on PACAP transcriptional response. PACAP induced transcription from the PACAP promoter through PACAP type I receptor (PAC1 receptor). PACAP gene transcription was also induced by NGF. Simultaneous treatment with PACAP and NGF resulted in a synergistic transcriptional response that was more than three times the predicted response, based on a simple additive effect of both agents. This synergism in transcriptional response paralleled the PACAP mRNA levels, as determined by RT‐PCR and northern blotting. The level of PACAP mRNA peaked 3 h after stimulation and gradually returned to basal levels by 48 h. PC12 cells are known to express predominantly the hop isoform of the PAC1 receptor, which positively couples to both adenylate cyclase and phospholipase C. To determine the role of the cyclic AMP and protein kinase C pathways in PACAP gene expression, the effects of forskolin and phorbol 12‐myristate 13‐acetate (PMA) were then examined. PMA did not alter PACAP mRNA levels but enhanced forskolin‐induced PACAP mRNA expression. Down‐regulation of protein kinase C blocked the ability of PACAP to stimulate PACAP mRNA expression. The mitogen‐activated protein kinase extracellular signal‐regulated kinase (ERK) kinase 1/2 (MEK1/2) inhibitor PD98059 also blocked the PACAP mRNA expression induced by either PACAP or NGF but not that induced by a combination of PACAP and NGF. These results suggest that PACAP stimulates the PACAP gene expression in PC12 cells at least in part through activation of adenylate cyclase and protein kinase C signaling pathways and that the ERK1/2 cascade is involved in PACAP and NGF‐induced PACAP gene expression, although redundant signaling pathways may also be involved. The present finding showing that PACAP in combination with NGF causes a synergistic increase in PACAP gene expression in PC12 cells supports the idea that PACAP acts as an autocrine regulatory factor.
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PC12 cells transfected with a PACAP promoter‐luciferase reporter construct were utilized to investigate the effects of PACAP, either alone or in combination with nerve growth factor (NGF), on PACAP transcriptional response. PACAP induced transcription from the PACAP promoter through PACAP type I receptor (PAC1 receptor). PACAP gene transcription was also induced by NGF. Simultaneous treatment with PACAP and NGF resulted in a synergistic transcriptional response that was more than three times the predicted response, based on a simple additive effect of both agents. This synergism in transcriptional response paralleled the PACAP mRNA levels, as determined by RT‐PCR and northern blotting. The level of PACAP mRNA peaked 3 h after stimulation and gradually returned to basal levels by 48 h. PC12 cells are known to express predominantly the hop isoform of the PAC1 receptor, which positively couples to both adenylate cyclase and phospholipase C. To determine the role of the cyclic AMP and protein kinase C pathways in PACAP gene expression, the effects of forskolin and phorbol 12‐myristate 13‐acetate (PMA) were then examined. PMA did not alter PACAP mRNA levels but enhanced forskolin‐induced PACAP mRNA expression. Down‐regulation of protein kinase C blocked the ability of PACAP to stimulate PACAP mRNA expression. The mitogen‐activated protein kinase extracellular signal‐regulated kinase (ERK) kinase 1/2 (MEK1/2) inhibitor PD98059 also blocked the PACAP mRNA expression induced by either PACAP or NGF but not that induced by a combination of PACAP and NGF. These results suggest that PACAP stimulates the PACAP gene expression in PC12 cells at least in part through activation of adenylate cyclase and protein kinase C signaling pathways and that the ERK1/2 cascade is involved in PACAP and NGF‐induced PACAP gene expression, although redundant signaling pathways may also be involved. The present finding showing that PACAP in combination with NGF causes a synergistic increase in PACAP gene expression in PC12 cells supports the idea that PACAP acts as an autocrine regulatory factor.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.2000.740501.x</identifier><identifier>PMID: 10646500</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford UK: Blackwell Science Ltd</publisher><subject>Animals ; Biological and medical sciences ; Blotting, Northern ; Colforsin - pharmacology ; Drug Synergism ; Enzyme Inhibitors - pharmacology ; Fundamental and applied biological sciences. 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PC12 cells transfected with a PACAP promoter‐luciferase reporter construct were utilized to investigate the effects of PACAP, either alone or in combination with nerve growth factor (NGF), on PACAP transcriptional response. PACAP induced transcription from the PACAP promoter through PACAP type I receptor (PAC1 receptor). PACAP gene transcription was also induced by NGF. Simultaneous treatment with PACAP and NGF resulted in a synergistic transcriptional response that was more than three times the predicted response, based on a simple additive effect of both agents. This synergism in transcriptional response paralleled the PACAP mRNA levels, as determined by RT‐PCR and northern blotting. The level of PACAP mRNA peaked 3 h after stimulation and gradually returned to basal levels by 48 h. PC12 cells are known to express predominantly the hop isoform of the PAC1 receptor, which positively couples to both adenylate cyclase and phospholipase C. To determine the role of the cyclic AMP and protein kinase C pathways in PACAP gene expression, the effects of forskolin and phorbol 12‐myristate 13‐acetate (PMA) were then examined. PMA did not alter PACAP mRNA levels but enhanced forskolin‐induced PACAP mRNA expression. Down‐regulation of protein kinase C blocked the ability of PACAP to stimulate PACAP mRNA expression. The mitogen‐activated protein kinase extracellular signal‐regulated kinase (ERK) kinase 1/2 (MEK1/2) inhibitor PD98059 also blocked the PACAP mRNA expression induced by either PACAP or NGF but not that induced by a combination of PACAP and NGF. These results suggest that PACAP stimulates the PACAP gene expression in PC12 cells at least in part through activation of adenylate cyclase and protein kinase C signaling pathways and that the ERK1/2 cascade is involved in PACAP and NGF‐induced PACAP gene expression, although redundant signaling pathways may also be involved. The present finding showing that PACAP in combination with NGF causes a synergistic increase in PACAP gene expression in PC12 cells supports the idea that PACAP acts as an autocrine regulatory factor.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Colforsin - pharmacology</subject><subject>Drug Synergism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression - drug effects</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>mRNA</subject><subject>Nerve growth factor</subject><subject>Nerve Growth Factor - pharmacology</subject><subject>Neuropeptides - genetics</subject><subject>Neuropeptides - pharmacology</subject><subject>PC12 Cells</subject><subject>Pituitary Adenylate Cyclase-Activating Polypeptide</subject><subject>Promoter activity</subject><subject>Rats</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Transcription. Transcription factor. Splicing. Rna processing</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAUhS0EokPhFZCREIJFgh3b-VlGUTsUVSUSsLYc56Z4lHEG22knOx6BBU_Ik5CQEbBkZV_7u_cenYPQC0piSnj6dhdTntGIU1HECSEkzjgRhMbHB2jz5-ch2hCSJBEjPDlDT7zfEUJTntLH6IyS-SII2aAfHycL7tb4YDS-su2ogxksHjpcmzCaoNyEyxbs1KsAuJp0rzz8_Pa9nLk7FYy9xfXQTwc4BNMCfl2XVVm_wVuwgC-OBwfeL_OaCd-AuwO8dcN9-IIvlQ6Dw8q2-HcHNhbXFU1wBX3vn6JHneo9PDud5-jz5cWn6l10_WF7VZXXkRY8p1HBQfNOFKLNWCsSxVjOCW2apMiy2RE1P6Vc8DbP6FyrJuVdmghOdJ4DayBj5-jVOvfghq8j-CD3xutZgbIwjF7SjLOcsQUsVlC7wXsHnTw4s5-9kZTIJRK5k4vxcjFeLpHINRJ5nHufn5aMzR7afzrXDGbg5QlQXqu-c8pq4_9yiRBpsWgoV-ze9DD9vwD5_qYia8F-AVS_p3I</recordid><startdate>200002</startdate><enddate>200002</enddate><creator>Hashimoto, Hitoshi</creator><creator>Hagihara, Nami</creator><creator>Koga, Kazumi</creator><creator>Yamamoto, Kyohei</creator><creator>Shintani, Norihito</creator><creator>Tomimoto, Shuhei</creator><creator>Mori, Wakaba</creator><creator>Koyama, Yutaka</creator><creator>Matsuda, Toshio</creator><creator>Baba, Akemichi</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>200002</creationdate><title>Synergistic Induction of Pituitary Adenylate Cyclase‐Activating Polypeptide (PACAP) Gene Expression by Nerve Growth Factor and PACAP in PC12 Cells</title><author>Hashimoto, Hitoshi ; Hagihara, Nami ; Koga, Kazumi ; Yamamoto, Kyohei ; Shintani, Norihito ; Tomimoto, Shuhei ; Mori, Wakaba ; Koyama, Yutaka ; Matsuda, Toshio ; Baba, Akemichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5481-94ec4f595d73d52a338401bb2977740a52a6454d871774ab64f62540c88e3be73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Colforsin - pharmacology</topic><topic>Drug Synergism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression - drug effects</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>mRNA</topic><topic>Nerve growth factor</topic><topic>Nerve Growth Factor - pharmacology</topic><topic>Neuropeptides - genetics</topic><topic>Neuropeptides - pharmacology</topic><topic>PC12 Cells</topic><topic>Pituitary Adenylate Cyclase-Activating Polypeptide</topic><topic>Promoter activity</topic><topic>Rats</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Transcription. Transcription factor. Splicing. Rna processing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashimoto, Hitoshi</creatorcontrib><creatorcontrib>Hagihara, Nami</creatorcontrib><creatorcontrib>Koga, Kazumi</creatorcontrib><creatorcontrib>Yamamoto, Kyohei</creatorcontrib><creatorcontrib>Shintani, Norihito</creatorcontrib><creatorcontrib>Tomimoto, Shuhei</creatorcontrib><creatorcontrib>Mori, Wakaba</creatorcontrib><creatorcontrib>Koyama, Yutaka</creatorcontrib><creatorcontrib>Matsuda, Toshio</creatorcontrib><creatorcontrib>Baba, Akemichi</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>Hashimoto, Hitoshi</au><au>Hagihara, Nami</au><au>Koga, Kazumi</au><au>Yamamoto, Kyohei</au><au>Shintani, Norihito</au><au>Tomimoto, Shuhei</au><au>Mori, Wakaba</au><au>Koyama, Yutaka</au><au>Matsuda, Toshio</au><au>Baba, Akemichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synergistic Induction of Pituitary Adenylate Cyclase‐Activating Polypeptide (PACAP) Gene Expression by Nerve Growth Factor and PACAP in PC12 Cells</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2000-02</date><risdate>2000</risdate><volume>74</volume><issue>2</issue><spage>501</spage><epage>507</epage><pages>501-507</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: Pituitary adenylate cyclase‐activating polypeptide (PACAP) gene expression was analyzed in PC12 cells. PC12 cells transfected with a PACAP promoter‐luciferase reporter construct were utilized to investigate the effects of PACAP, either alone or in combination with nerve growth factor (NGF), on PACAP transcriptional response. PACAP induced transcription from the PACAP promoter through PACAP type I receptor (PAC1 receptor). PACAP gene transcription was also induced by NGF. Simultaneous treatment with PACAP and NGF resulted in a synergistic transcriptional response that was more than three times the predicted response, based on a simple additive effect of both agents. This synergism in transcriptional response paralleled the PACAP mRNA levels, as determined by RT‐PCR and northern blotting. The level of PACAP mRNA peaked 3 h after stimulation and gradually returned to basal levels by 48 h. PC12 cells are known to express predominantly the hop isoform of the PAC1 receptor, which positively couples to both adenylate cyclase and phospholipase C. To determine the role of the cyclic AMP and protein kinase C pathways in PACAP gene expression, the effects of forskolin and phorbol 12‐myristate 13‐acetate (PMA) were then examined. PMA did not alter PACAP mRNA levels but enhanced forskolin‐induced PACAP mRNA expression. Down‐regulation of protein kinase C blocked the ability of PACAP to stimulate PACAP mRNA expression. The mitogen‐activated protein kinase extracellular signal‐regulated kinase (ERK) kinase 1/2 (MEK1/2) inhibitor PD98059 also blocked the PACAP mRNA expression induced by either PACAP or NGF but not that induced by a combination of PACAP and NGF. These results suggest that PACAP stimulates the PACAP gene expression in PC12 cells at least in part through activation of adenylate cyclase and protein kinase C signaling pathways and that the ERK1/2 cascade is involved in PACAP and NGF‐induced PACAP gene expression, although redundant signaling pathways may also be involved. The present finding showing that PACAP in combination with NGF causes a synergistic increase in PACAP gene expression in PC12 cells supports the idea that PACAP acts as an autocrine regulatory factor.</abstract><cop>Oxford UK</cop><pub>Blackwell Science Ltd</pub><pmid>10646500</pmid><doi>10.1046/j.1471-4159.2000.740501.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library Free Content; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; IngentaConnect Free/Open Access Journals; Free Full-Text Journals in Chemistry
subjects Animals
Biological and medical sciences
Blotting, Northern
Colforsin - pharmacology
Drug Synergism
Enzyme Inhibitors - pharmacology
Fundamental and applied biological sciences. Psychology
Gene Expression - drug effects
Mice
Molecular and cellular biology
Molecular genetics
mRNA
Nerve growth factor
Nerve Growth Factor - pharmacology
Neuropeptides - genetics
Neuropeptides - pharmacology
PC12 Cells
Pituitary Adenylate Cyclase-Activating Polypeptide
Promoter activity
Rats
Reverse Transcriptase Polymerase Chain Reaction
Tetradecanoylphorbol Acetate - pharmacology
Transcription. Transcription factor. Splicing. Rna processing
title Synergistic Induction of Pituitary Adenylate Cyclase‐Activating Polypeptide (PACAP) Gene Expression by Nerve Growth Factor and PACAP in PC12 Cells
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