MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression

Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Journal of biological chemistry 2016-02, Vol.291 (8), p.3959-3966
Hauptverfasser: Kushwaha, Priyanka, Khedgikar, Vikram, Sharma, Deepika, Yuen, Tony, Gautam, Jyoti, Ahmad, Naseer, Karvande, Anirudha, Mishra, Prabhat R., Trivedi, Prabodh K., Sun, Li, Bhadada, Sanjay K., Zaidi, Mone, Trivedi, Ritu
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3966
container_issue 8
container_start_page 3959
container_title The Journal of biological chemistry
container_volume 291
creator Kushwaha, Priyanka
Khedgikar, Vikram
Sharma, Deepika
Yuen, Tony
Gautam, Jyoti
Ahmad, Naseer
Karvande, Anirudha
Mishra, Prabhat R.
Trivedi, Prabodh K.
Sun, Li
Bhadada, Sanjay K.
Zaidi, Mone
Trivedi, Ritu
description Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.
doi_str_mv 10.1074/jbc.M115.687152
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4759174</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925820437032</els_id><sourcerecordid>1767067178</sourcerecordid><originalsourceid>FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</originalsourceid><addsrcrecordid>eNp1kUFv1DAQRi0EotvCmRvKkUu2ntix4wvSqlooUluktghuluNMFpesE-ykYv99HaVU5YAvI3ueP1vzCHkHdA1U8tO72q4vAcq1qCSUxQuyAlqxnJXw4yVZUVpAroqyOiLHMd7RtLiC1-SoEEIwWskV8ZfOhv76apNVkudsyLZ_MIwxu_mFHY6myzbe1H3nbLZtW7Spsx3cDj2OzpquO2TNFJzfZd_R-LnWh-xmGoaAMc7b88ZYSJnLQe_fkFet6SK-fawn5Nun7e3ZeX7x9fOXs81FbjlnY24LDkhZW1pqoaisakSDhlkFhirEGoAzbMECY4LWWDKqWEUFqwqurEDOTsjHJXeY6j02Fv0YTKeH4PYmHHRvnP63491PvevvNZelAjkHfHgMCP3vCeOo9y5a7DrjsZ-iBikkFRJkldDTBU2DjDFg-_QMUD1b0smSni3pxVK68f757574v1oSoBYA04zuHQYdrUNvsXEhSdBN7_4b_gBufaIP</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1767067178</pqid></control><display><type>article</type><title>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Kushwaha, Priyanka ; Khedgikar, Vikram ; Sharma, Deepika ; Yuen, Tony ; Gautam, Jyoti ; Ahmad, Naseer ; Karvande, Anirudha ; Mishra, Prabhat R. ; Trivedi, Prabodh K. ; Sun, Li ; Bhadada, Sanjay K. ; Zaidi, Mone ; Trivedi, Ritu</creator><creatorcontrib>Kushwaha, Priyanka ; Khedgikar, Vikram ; Sharma, Deepika ; Yuen, Tony ; Gautam, Jyoti ; Ahmad, Naseer ; Karvande, Anirudha ; Mishra, Prabhat R. ; Trivedi, Prabodh K. ; Sun, Li ; Bhadada, Sanjay K. ; Zaidi, Mone ; Trivedi, Ritu</creatorcontrib><description>Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M115.687152</identifier><identifier>PMID: 26663087</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>animal model ; Animals ; bone ; bone morphogenetic protein (BMP) ; Calcification, Physiologic - physiology ; cell differentiation ; Cell Differentiation - physiology ; Core Binding Factor Alpha 1 Subunit - biosynthesis ; Core Binding Factor Alpha 1 Subunit - genetics ; drug discovery ; Epigenesis, Genetic - physiology ; Female ; Gene Expression Regulation, Enzymologic - physiology ; Gene Regulation ; gene silencing ; histone deacetylase 1 (HDAC1) ; Histone Deacetylase 1 - genetics ; Histone Deacetylase 1 - metabolism ; Mice ; microRNA (miRNA) ; MicroRNAs - genetics ; MicroRNAs - metabolism ; osteoblast ; Osteoblasts - cytology ; Osteoblasts - metabolism ; osteoporosis ; Pregnancy ; Weaning</subject><ispartof>The Journal of biological chemistry, 2016-02, Vol.291 (8), p.3959-3966</ispartof><rights>2016 © 2016 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc. 2016 The American Society for Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</citedby><cites>FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</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/PMC4759174/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759174/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26663087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kushwaha, Priyanka</creatorcontrib><creatorcontrib>Khedgikar, Vikram</creatorcontrib><creatorcontrib>Sharma, Deepika</creatorcontrib><creatorcontrib>Yuen, Tony</creatorcontrib><creatorcontrib>Gautam, Jyoti</creatorcontrib><creatorcontrib>Ahmad, Naseer</creatorcontrib><creatorcontrib>Karvande, Anirudha</creatorcontrib><creatorcontrib>Mishra, Prabhat R.</creatorcontrib><creatorcontrib>Trivedi, Prabodh K.</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Bhadada, Sanjay K.</creatorcontrib><creatorcontrib>Zaidi, Mone</creatorcontrib><creatorcontrib>Trivedi, Ritu</creatorcontrib><title>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</description><subject>animal model</subject><subject>Animals</subject><subject>bone</subject><subject>bone morphogenetic protein (BMP)</subject><subject>Calcification, Physiologic - physiology</subject><subject>cell differentiation</subject><subject>Cell Differentiation - physiology</subject><subject>Core Binding Factor Alpha 1 Subunit - biosynthesis</subject><subject>Core Binding Factor Alpha 1 Subunit - genetics</subject><subject>drug discovery</subject><subject>Epigenesis, Genetic - physiology</subject><subject>Female</subject><subject>Gene Expression Regulation, Enzymologic - physiology</subject><subject>Gene Regulation</subject><subject>gene silencing</subject><subject>histone deacetylase 1 (HDAC1)</subject><subject>Histone Deacetylase 1 - genetics</subject><subject>Histone Deacetylase 1 - metabolism</subject><subject>Mice</subject><subject>microRNA (miRNA)</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>osteoblast</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>osteoporosis</subject><subject>Pregnancy</subject><subject>Weaning</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQRi0EotvCmRvKkUu2ntix4wvSqlooUluktghuluNMFpesE-ykYv99HaVU5YAvI3ueP1vzCHkHdA1U8tO72q4vAcq1qCSUxQuyAlqxnJXw4yVZUVpAroqyOiLHMd7RtLiC1-SoEEIwWskV8ZfOhv76apNVkudsyLZ_MIwxu_mFHY6myzbe1H3nbLZtW7Spsx3cDj2OzpquO2TNFJzfZd_R-LnWh-xmGoaAMc7b88ZYSJnLQe_fkFet6SK-fawn5Nun7e3ZeX7x9fOXs81FbjlnY24LDkhZW1pqoaisakSDhlkFhirEGoAzbMECY4LWWDKqWEUFqwqurEDOTsjHJXeY6j02Fv0YTKeH4PYmHHRvnP63491PvevvNZelAjkHfHgMCP3vCeOo9y5a7DrjsZ-iBikkFRJkldDTBU2DjDFg-_QMUD1b0smSni3pxVK68f757574v1oSoBYA04zuHQYdrUNvsXEhSdBN7_4b_gBufaIP</recordid><startdate>20160219</startdate><enddate>20160219</enddate><creator>Kushwaha, Priyanka</creator><creator>Khedgikar, Vikram</creator><creator>Sharma, Deepika</creator><creator>Yuen, Tony</creator><creator>Gautam, Jyoti</creator><creator>Ahmad, Naseer</creator><creator>Karvande, Anirudha</creator><creator>Mishra, Prabhat R.</creator><creator>Trivedi, Prabodh K.</creator><creator>Sun, Li</creator><creator>Bhadada, Sanjay K.</creator><creator>Zaidi, Mone</creator><creator>Trivedi, Ritu</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>20160219</creationdate><title>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</title><author>Kushwaha, Priyanka ; Khedgikar, Vikram ; Sharma, Deepika ; Yuen, Tony ; Gautam, Jyoti ; Ahmad, Naseer ; Karvande, Anirudha ; Mishra, Prabhat R. ; Trivedi, Prabodh K. ; Sun, Li ; Bhadada, Sanjay K. ; Zaidi, Mone ; Trivedi, Ritu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-c241e03f5c0c128c9d6dea3c91a09eeb1143ef1c13360be5309380638249c6e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>animal model</topic><topic>Animals</topic><topic>bone</topic><topic>bone morphogenetic protein (BMP)</topic><topic>Calcification, Physiologic - physiology</topic><topic>cell differentiation</topic><topic>Cell Differentiation - physiology</topic><topic>Core Binding Factor Alpha 1 Subunit - biosynthesis</topic><topic>Core Binding Factor Alpha 1 Subunit - genetics</topic><topic>drug discovery</topic><topic>Epigenesis, Genetic - physiology</topic><topic>Female</topic><topic>Gene Expression Regulation, Enzymologic - physiology</topic><topic>Gene Regulation</topic><topic>gene silencing</topic><topic>histone deacetylase 1 (HDAC1)</topic><topic>Histone Deacetylase 1 - genetics</topic><topic>Histone Deacetylase 1 - metabolism</topic><topic>Mice</topic><topic>microRNA (miRNA)</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>osteoblast</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>osteoporosis</topic><topic>Pregnancy</topic><topic>Weaning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kushwaha, Priyanka</creatorcontrib><creatorcontrib>Khedgikar, Vikram</creatorcontrib><creatorcontrib>Sharma, Deepika</creatorcontrib><creatorcontrib>Yuen, Tony</creatorcontrib><creatorcontrib>Gautam, Jyoti</creatorcontrib><creatorcontrib>Ahmad, Naseer</creatorcontrib><creatorcontrib>Karvande, Anirudha</creatorcontrib><creatorcontrib>Mishra, Prabhat R.</creatorcontrib><creatorcontrib>Trivedi, Prabodh K.</creatorcontrib><creatorcontrib>Sun, Li</creatorcontrib><creatorcontrib>Bhadada, Sanjay K.</creatorcontrib><creatorcontrib>Zaidi, Mone</creatorcontrib><creatorcontrib>Trivedi, Ritu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kushwaha, Priyanka</au><au>Khedgikar, Vikram</au><au>Sharma, Deepika</au><au>Yuen, Tony</au><au>Gautam, Jyoti</au><au>Ahmad, Naseer</au><au>Karvande, Anirudha</au><au>Mishra, Prabhat R.</au><au>Trivedi, Prabodh K.</au><au>Sun, Li</au><au>Bhadada, Sanjay K.</au><au>Zaidi, Mone</au><au>Trivedi, Ritu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2016-02-19</date><risdate>2016</risdate><volume>291</volume><issue>8</issue><spage>3959</spage><epage>3966</epage><pages>3959-3966</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26663087</pmid><doi>10.1074/jbc.M115.687152</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2016-02, Vol.291 (8), p.3959-3966
issn 0021-9258
1083-351X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4759174
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection
subjects animal model
Animals
bone
bone morphogenetic protein (BMP)
Calcification, Physiologic - physiology
cell differentiation
Cell Differentiation - physiology
Core Binding Factor Alpha 1 Subunit - biosynthesis
Core Binding Factor Alpha 1 Subunit - genetics
drug discovery
Epigenesis, Genetic - physiology
Female
Gene Expression Regulation, Enzymologic - physiology
Gene Regulation
gene silencing
histone deacetylase 1 (HDAC1)
Histone Deacetylase 1 - genetics
Histone Deacetylase 1 - metabolism
Mice
microRNA (miRNA)
MicroRNAs - genetics
MicroRNAs - metabolism
osteoblast
Osteoblasts - cytology
Osteoblasts - metabolism
osteoporosis
Pregnancy
Weaning
title MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T10%3A24%3A54IST&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=MicroRNA%20874-3p%20Exerts%20Skeletal%20Anabolic%20Effects%20Epigenetically%20during%20Weaning%20by%20Suppressing%20Hdac1%20Expression&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Kushwaha,%20Priyanka&rft.date=2016-02-19&rft.volume=291&rft.issue=8&rft.spage=3959&rft.epage=3966&rft.pages=3959-3966&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M115.687152&rft_dat=%3Cproquest_pubme%3E1767067178%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=1767067178&rft_id=info:pmid/26663087&rft_els_id=S0021925820437032&rfr_iscdi=true