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Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation
Osteocytes are critical mechanosensory cells in bone, and mechanically stimulated osteocytes produce exosomes that can induce osteogenesis. MicroRNAs (miRNAs) are important constituents of exosomes, and some miRNAs in osteocytes regulate osteogenic differentiation; previous studies have indicated th...
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Published in: | Biomedical engineering online 2024-05, Vol.23 (1), p.44-44, Article 44 |
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description | Osteocytes are critical mechanosensory cells in bone, and mechanically stimulated osteocytes produce exosomes that can induce osteogenesis. MicroRNAs (miRNAs) are important constituents of exosomes, and some miRNAs in osteocytes regulate osteogenic differentiation; previous studies have indicated that some differentially expressed miRNAs in mechanically strained osteocytes likely influence osteoblastic differentiation. Therefore, screening and selection of miRNAs that regulate osteogenic differentiation in exosomes of mechanically stimulated osteocytes are important.
A mechanical tensile strain of 2500 με at 0.5 Hz 1 h per day for 3 days, elevated prostaglandin E2 (PGE2) and insulin-like growth factor-1 (IGF-1) levels and nitric oxide synthase (NOS) activity of MLO-Y4 osteocytes, and promoted osteogenic differentiation of MC3T3-E1 osteoblasts. Fourteen miRNAs differentially expressed only in MLO-Y4 osteocytes which were stimulated with mechanical tensile strain, were screened, and the miRNAs related to osteogenesis were identified. Four differentially expressed miRNAs (miR-1930-3p, miR-3110-5p, miR-3090-3p, and miR-3058-3p) were found only in mechanically strained osteocytes, and the four miRNAs, eight targeted mRNAs which were differentially expressed only in mechanically strained osteoblasts, were also identified. In addition, the mechanically strained osteocyte-derived exosomes promoted the osteoblastic differentiation of MC3T3-E1 cells in vitro, the exosomes were internalized by osteoblasts, and the up-regulated miR-3110-5p and miR-3058-3p in mechanically strained osteocytes, were both increased in the exosomes, which was verified via reverse transcription quantitative polymerase chain reaction (RT-qPCR).
In osteocytes, a mechanical tensile strain of 2500 με at 0.5 Hz induced the fourteen differentially expressed miRNAs which probably were in exosomes of osteocytes and involved in osteogenesis. The mechanically strained osteocyte-derived exosomes which contained increased miR-3110-5p and miR-3058-3p (two of the 14 miRNAs), promoted osteoblastic differentiation. |
doi_str_mv | 10.1186/s12938-024-01237-9 |
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A mechanical tensile strain of 2500 με at 0.5 Hz 1 h per day for 3 days, elevated prostaglandin E2 (PGE2) and insulin-like growth factor-1 (IGF-1) levels and nitric oxide synthase (NOS) activity of MLO-Y4 osteocytes, and promoted osteogenic differentiation of MC3T3-E1 osteoblasts. Fourteen miRNAs differentially expressed only in MLO-Y4 osteocytes which were stimulated with mechanical tensile strain, were screened, and the miRNAs related to osteogenesis were identified. Four differentially expressed miRNAs (miR-1930-3p, miR-3110-5p, miR-3090-3p, and miR-3058-3p) were found only in mechanically strained osteocytes, and the four miRNAs, eight targeted mRNAs which were differentially expressed only in mechanically strained osteoblasts, were also identified. In addition, the mechanically strained osteocyte-derived exosomes promoted the osteoblastic differentiation of MC3T3-E1 cells in vitro, the exosomes were internalized by osteoblasts, and the up-regulated miR-3110-5p and miR-3058-3p in mechanically strained osteocytes, were both increased in the exosomes, which was verified via reverse transcription quantitative polymerase chain reaction (RT-qPCR).
In osteocytes, a mechanical tensile strain of 2500 με at 0.5 Hz induced the fourteen differentially expressed miRNAs which probably were in exosomes of osteocytes and involved in osteogenesis. The mechanically strained osteocyte-derived exosomes which contained increased miR-3110-5p and miR-3058-3p (two of the 14 miRNAs), promoted osteoblastic differentiation.</description><identifier>ISSN: 1475-925X</identifier><identifier>EISSN: 1475-925X</identifier><identifier>DOI: 10.1186/s12938-024-01237-9</identifier><identifier>PMID: 38705993</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Animals ; Bioinformatics ; Bone cells ; Bones ; Cell Differentiation ; Cell Line ; Differentiation (biology) ; Evaluation ; Exosomes ; Exosomes - metabolism ; Gene expression ; Gene Expression Regulation ; Growth factors ; Health aspects ; Homeostasis ; Insulin-like growth factor I ; Insulin-like growth factors ; Mechanical strain ; Mice ; MicroRNA ; MicroRNAs ; MicroRNAs - genetics ; MicroRNAs - metabolism ; Microscopy ; miRNA ; Nitric oxide ; Nitric-oxide synthase ; Osteoblastogenesis ; Osteoblasts ; Osteoblasts - cytology ; Osteoblasts - metabolism ; Osteocyte ; Osteocytes ; Osteocytes - cytology ; Osteocytes - metabolism ; Osteogenesis ; Osteogenesis - genetics ; Polymerase chain reaction ; Prostaglandin E2 ; Prostaglandins E ; Proteins ; Reverse transcription ; Stem cells ; Stress, Mechanical ; Tensile strain</subject><ispartof>Biomedical engineering online, 2024-05, Vol.23 (1), p.44-44, Article 44</ispartof><rights>2024. The Author(s).</rights><rights>COPYRIGHT 2024 BioMed Central Ltd.</rights><rights>2024. This work is licensed 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><rights>The Author(s) 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c549t-d3faa2c33632425ad216da9694f62a601d7e8ce4c6ced753ca1b2686bc7b70ae3</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/PMC11070085/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3054192618?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38705993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yingwen</creatorcontrib><creatorcontrib>Li, Yanan</creatorcontrib><creatorcontrib>Cao, Zhen</creatorcontrib><creatorcontrib>Xue, Jindong</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Hu, Tingting</creatorcontrib><creatorcontrib>Han, Biao</creatorcontrib><creatorcontrib>Guo, Yong</creatorcontrib><title>Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation</title><title>Biomedical engineering online</title><addtitle>Biomed Eng Online</addtitle><description>Osteocytes are critical mechanosensory cells in bone, and mechanically stimulated osteocytes produce exosomes that can induce osteogenesis. MicroRNAs (miRNAs) are important constituents of exosomes, and some miRNAs in osteocytes regulate osteogenic differentiation; previous studies have indicated that some differentially expressed miRNAs in mechanically strained osteocytes likely influence osteoblastic differentiation. Therefore, screening and selection of miRNAs that regulate osteogenic differentiation in exosomes of mechanically stimulated osteocytes are important.
A mechanical tensile strain of 2500 με at 0.5 Hz 1 h per day for 3 days, elevated prostaglandin E2 (PGE2) and insulin-like growth factor-1 (IGF-1) levels and nitric oxide synthase (NOS) activity of MLO-Y4 osteocytes, and promoted osteogenic differentiation of MC3T3-E1 osteoblasts. Fourteen miRNAs differentially expressed only in MLO-Y4 osteocytes which were stimulated with mechanical tensile strain, were screened, and the miRNAs related to osteogenesis were identified. Four differentially expressed miRNAs (miR-1930-3p, miR-3110-5p, miR-3090-3p, and miR-3058-3p) were found only in mechanically strained osteocytes, and the four miRNAs, eight targeted mRNAs which were differentially expressed only in mechanically strained osteoblasts, were also identified. In addition, the mechanically strained osteocyte-derived exosomes promoted the osteoblastic differentiation of MC3T3-E1 cells in vitro, the exosomes were internalized by osteoblasts, and the up-regulated miR-3110-5p and miR-3058-3p in mechanically strained osteocytes, were both increased in the exosomes, which was verified via reverse transcription quantitative polymerase chain reaction (RT-qPCR).
In osteocytes, a mechanical tensile strain of 2500 με at 0.5 Hz induced the fourteen differentially expressed miRNAs which probably were in exosomes of osteocytes and involved in osteogenesis. The mechanically strained osteocyte-derived exosomes which contained increased miR-3110-5p and miR-3058-3p (two of the 14 miRNAs), promoted osteoblastic differentiation.</description><subject>Analysis</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Bone cells</subject><subject>Bones</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Differentiation (biology)</subject><subject>Evaluation</subject><subject>Exosomes</subject><subject>Exosomes - metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Growth factors</subject><subject>Health aspects</subject><subject>Homeostasis</subject><subject>Insulin-like growth factor I</subject><subject>Insulin-like growth factors</subject><subject>Mechanical strain</subject><subject>Mice</subject><subject>MicroRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - genetics</subject><subject>MicroRNAs - metabolism</subject><subject>Microscopy</subject><subject>miRNA</subject><subject>Nitric oxide</subject><subject>Nitric-oxide synthase</subject><subject>Osteoblastogenesis</subject><subject>Osteoblasts</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>Osteocyte</subject><subject>Osteocytes</subject><subject>Osteocytes - cytology</subject><subject>Osteocytes - metabolism</subject><subject>Osteogenesis</subject><subject>Osteogenesis - genetics</subject><subject>Polymerase chain reaction</subject><subject>Prostaglandin E2</subject><subject>Prostaglandins E</subject><subject>Proteins</subject><subject>Reverse transcription</subject><subject>Stem cells</subject><subject>Stress, Mechanical</subject><subject>Tensile strain</subject><issn>1475-925X</issn><issn>1475-925X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkktv1DAUhSMEoqXwB1igkdjAIsWPxI5XqKp4jFSEVEBiZ93YN1OPkniwPVVnx0_Haaalg1AWjq-_e5J7fIriJSWnlDbiXaRM8aYkrCoJZVyW6lFxTCtZl4rVPx8_eD8qnsW4JoQRItTT4og3ktRK8ePi9xc0VzA6A32_W8QUwI1oFz4m9GaXsLQY3HWu4I2PfsC4MH5MMzS4y5JTSsp6s4Bxvyd1U_J5vwl-8OlOre0hJmcW1nUdBhyTg-T8-Lx40kEf8cV-PSl-fPzw_fxzefH10_L87KI0daVSaXkHwAzngrOK1WAZFRaUUFUnGAhCrcTGYGWEQStrboC2TDSiNbKVBJCfFMtZ13pY601wA4Sd9uD0bcGHlYaQ_69HrTqUVNpK0U5UlnEFIFlNRKvqpiKNylrvZ63Nth3QmjxMgP5A9PBkdFd65a91NksS0tRZ4c1eIfhfW4xJDy4a7HsY0W-jzjbSPCYnIqOv_0HXfhvG7NVEVVQxQZu_1AryBG7sfP6wmUT1mVSckkYQnqnT_1D5sTi4fLHYuVw_aHh70DBdPt6kFWxj1Mtvl4csm1kTfIwBu3tDKNFTYPUcWJ0Dq28DqycrXz208r7lLqH8DwMX5IM</recordid><startdate>20240505</startdate><enddate>20240505</enddate><creator>Zhu, Yingwen</creator><creator>Li, Yanan</creator><creator>Cao, Zhen</creator><creator>Xue, Jindong</creator><creator>Wang, Xiaoyan</creator><creator>Hu, Tingting</creator><creator>Han, Biao</creator><creator>Guo, Yong</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><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>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240505</creationdate><title>Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation</title><author>Zhu, Yingwen ; Li, Yanan ; Cao, Zhen ; Xue, Jindong ; Wang, Xiaoyan ; Hu, Tingting ; Han, Biao ; Guo, Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-d3faa2c33632425ad216da9694f62a601d7e8ce4c6ced753ca1b2686bc7b70ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Analysis</topic><topic>Animals</topic><topic>Bioinformatics</topic><topic>Bone cells</topic><topic>Bones</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Differentiation (biology)</topic><topic>Evaluation</topic><topic>Exosomes</topic><topic>Exosomes - metabolism</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Growth factors</topic><topic>Health aspects</topic><topic>Homeostasis</topic><topic>Insulin-like growth factor I</topic><topic>Insulin-like growth factors</topic><topic>Mechanical strain</topic><topic>Mice</topic><topic>MicroRNA</topic><topic>MicroRNAs</topic><topic>MicroRNAs - genetics</topic><topic>MicroRNAs - metabolism</topic><topic>Microscopy</topic><topic>miRNA</topic><topic>Nitric oxide</topic><topic>Nitric-oxide synthase</topic><topic>Osteoblastogenesis</topic><topic>Osteoblasts</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>Osteocyte</topic><topic>Osteocytes</topic><topic>Osteocytes - cytology</topic><topic>Osteocytes - metabolism</topic><topic>Osteogenesis</topic><topic>Osteogenesis - genetics</topic><topic>Polymerase chain reaction</topic><topic>Prostaglandin E2</topic><topic>Prostaglandins E</topic><topic>Proteins</topic><topic>Reverse transcription</topic><topic>Stem cells</topic><topic>Stress, Mechanical</topic><topic>Tensile strain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yingwen</creatorcontrib><creatorcontrib>Li, Yanan</creatorcontrib><creatorcontrib>Cao, Zhen</creatorcontrib><creatorcontrib>Xue, Jindong</creatorcontrib><creatorcontrib>Wang, Xiaoyan</creatorcontrib><creatorcontrib>Hu, Tingting</creatorcontrib><creatorcontrib>Han, Biao</creatorcontrib><creatorcontrib>Guo, Yong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest - 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MicroRNAs (miRNAs) are important constituents of exosomes, and some miRNAs in osteocytes regulate osteogenic differentiation; previous studies have indicated that some differentially expressed miRNAs in mechanically strained osteocytes likely influence osteoblastic differentiation. Therefore, screening and selection of miRNAs that regulate osteogenic differentiation in exosomes of mechanically stimulated osteocytes are important.
A mechanical tensile strain of 2500 με at 0.5 Hz 1 h per day for 3 days, elevated prostaglandin E2 (PGE2) and insulin-like growth factor-1 (IGF-1) levels and nitric oxide synthase (NOS) activity of MLO-Y4 osteocytes, and promoted osteogenic differentiation of MC3T3-E1 osteoblasts. Fourteen miRNAs differentially expressed only in MLO-Y4 osteocytes which were stimulated with mechanical tensile strain, were screened, and the miRNAs related to osteogenesis were identified. Four differentially expressed miRNAs (miR-1930-3p, miR-3110-5p, miR-3090-3p, and miR-3058-3p) were found only in mechanically strained osteocytes, and the four miRNAs, eight targeted mRNAs which were differentially expressed only in mechanically strained osteoblasts, were also identified. In addition, the mechanically strained osteocyte-derived exosomes promoted the osteoblastic differentiation of MC3T3-E1 cells in vitro, the exosomes were internalized by osteoblasts, and the up-regulated miR-3110-5p and miR-3058-3p in mechanically strained osteocytes, were both increased in the exosomes, which was verified via reverse transcription quantitative polymerase chain reaction (RT-qPCR).
In osteocytes, a mechanical tensile strain of 2500 με at 0.5 Hz induced the fourteen differentially expressed miRNAs which probably were in exosomes of osteocytes and involved in osteogenesis. The mechanically strained osteocyte-derived exosomes which contained increased miR-3110-5p and miR-3058-3p (two of the 14 miRNAs), promoted osteoblastic differentiation.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>38705993</pmid><doi>10.1186/s12938-024-01237-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Bioinformatics Bone cells Bones Cell Differentiation Cell Line Differentiation (biology) Evaluation Exosomes Exosomes - metabolism Gene expression Gene Expression Regulation Growth factors Health aspects Homeostasis Insulin-like growth factor I Insulin-like growth factors Mechanical strain Mice MicroRNA MicroRNAs MicroRNAs - genetics MicroRNAs - metabolism Microscopy miRNA Nitric oxide Nitric-oxide synthase Osteoblastogenesis Osteoblasts Osteoblasts - cytology Osteoblasts - metabolism Osteocyte Osteocytes Osteocytes - cytology Osteocytes - metabolism Osteogenesis Osteogenesis - genetics Polymerase chain reaction Prostaglandin E2 Prostaglandins E Proteins Reverse transcription Stem cells Stress, Mechanical Tensile strain |
title | Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation |
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