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Human hair follicle transcriptome profiling: a minimally invasive tool to assess molecular adaptations upon low‐volume, high‐intensity interval training
High‐intensity interval training (HIIT) has become a popular fitness training approach under both civilian and military settings. Consisting of brief and intense exercise intervals, HIIT requires less time commitment yet is able to produce the consistent targeted physical adaptations as conventional...
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Published in: | Physiological reports 2017-12, Vol.5 (23), p.n/a |
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description | High‐intensity interval training (HIIT) has become a popular fitness training approach under both civilian and military settings. Consisting of brief and intense exercise intervals, HIIT requires less time commitment yet is able to produce the consistent targeted physical adaptations as conventional endurance training. To effectively characterize and monitor HIIT‐induced cellular and molecular responses, a highly accessible yet comprehensive biomarker discovery source is desirable. Both gene differential expression (DE) and gene set (GS) analyses were conducted using hair follicle transcriptome established from pre and postexercise subjects upon a 10‐day HIIT program by RNA‐Seq, Comparing between pre and posttraining groups, differentially expressed protein coding genes were identified. To interpret the functional significance of the DE results, a comprehensive GS analysis approach featuring multiple algorithms was used to enrich gene ontology (GO) terms and KEGG pathways. The GS analysis revealed enriched themes such as energy metabolism, cell proliferation/growth/survival, muscle adaptations, and cytokine–cytokine interaction, all of which have been previously proposed as HIIT responses. Moreover, related cell signaling pathways were also measured. Specifically, G‐protein‐mediated signal transduction, phosphatidylinositide 3‐kinases (PI3K) – protein kinase B (PKB) and Janus kinase (JAK) – Signal Transducer and Activator of Transcription (STAT) signaling cascades were over‐represented. Additionally, the RNA‐Seq analysis also identified several HIIT‐responsive microRNAs (miRNAs) that were involved in regulating hair follicle‐specific processes, such as miR‐99a. For the first time, this study demonstrated that both existing and new biomarkers like miRNA can be explored for HIIT using the transcriptomic responses exhibited by the hair follicle.
We propose scalp hair follicle as a minimally invasive yet comprehensive biomarker discovery system to effectively characterize and monitor HIIT‐induced cellular and molecular responses. For the first time, this study demonstrated that both existing and new biomarkers like miRNA could be explored for HIIT using the transcriptomic responses exhibited by the hair follicle, providing a foundation for additional HIIT evaluation measures. |
doi_str_mv | 10.14814/phy2.13534 |
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We propose scalp hair follicle as a minimally invasive yet comprehensive biomarker discovery system to effectively characterize and monitor HIIT‐induced cellular and molecular responses. For the first time, this study demonstrated that both existing and new biomarkers like miRNA could be explored for HIIT using the transcriptomic responses exhibited by the hair follicle, providing a foundation for additional HIIT evaluation measures.</description><identifier>EISSN: 2051-817X</identifier><identifier>DOI: 10.14814/phy2.13534</identifier><identifier>PMID: 29212859</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>1-Phosphatidylinositol 3-kinase ; Adaptation ; Adaptation, Physiological ; Adult ; AKT protein ; Biomarkers - metabolism ; Cell proliferation ; Cell survival ; Cytokines ; Endurance training ; Energy metabolism ; Gene expression ; Gene Expression Profiling - methods ; Hair ; Hair Follicle - metabolism ; High-Intensity Interval Training ; Humans ; Janus kinase ; Janus Kinases - genetics ; Janus Kinases - metabolism ; Kinases ; Male ; miRNA ; Molecular Diagnostic Techniques - methods ; muscle contraction ; Original Research ; Phosphatidylinositol 3-Kinases - genetics ; Phosphatidylinositol 3-Kinases - metabolism ; Physical fitness ; Physical training ; Physiology ; Proteins ; Proto-Oncogene Proteins c-akt - genetics ; Proto-Oncogene Proteins c-akt - metabolism ; Receptors, G-Protein-Coupled - genetics ; Receptors, G-Protein-Coupled - metabolism ; RNA‐Seq ; Signal Transduction ; STAT Transcription Factors - genetics ; STAT Transcription Factors - metabolism ; Transcription ; Transcriptome</subject><ispartof>Physiological reports, 2017-12, Vol.5 (23), p.n/a</ispartof><rights>2017 The Authors. published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society</rights><rights>2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society.</rights><rights>2017. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5184-bab5709c1ec294a2a797b993f256a03aca7ef0fc500a8a316e10fb0db03936103</citedby><cites>FETCH-LOGICAL-c5184-bab5709c1ec294a2a797b993f256a03aca7ef0fc500a8a316e10fb0db03936103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1975839205/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1975839205?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29212859$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Wallace, Sarah J.</creatorcontrib><creatorcontrib>Shiu, Maria Y.</creatorcontrib><creatorcontrib>Smith, Ingrid</creatorcontrib><creatorcontrib>Rhind, Shawn G.</creatorcontrib><creatorcontrib>Langlois, Valerie S.</creatorcontrib><title>Human hair follicle transcriptome profiling: a minimally invasive tool to assess molecular adaptations upon low‐volume, high‐intensity interval training</title><title>Physiological reports</title><addtitle>Physiol Rep</addtitle><description>High‐intensity interval training (HIIT) has become a popular fitness training approach under both civilian and military settings. Consisting of brief and intense exercise intervals, HIIT requires less time commitment yet is able to produce the consistent targeted physical adaptations as conventional endurance training. To effectively characterize and monitor HIIT‐induced cellular and molecular responses, a highly accessible yet comprehensive biomarker discovery source is desirable. Both gene differential expression (DE) and gene set (GS) analyses were conducted using hair follicle transcriptome established from pre and postexercise subjects upon a 10‐day HIIT program by RNA‐Seq, Comparing between pre and posttraining groups, differentially expressed protein coding genes were identified. To interpret the functional significance of the DE results, a comprehensive GS analysis approach featuring multiple algorithms was used to enrich gene ontology (GO) terms and KEGG pathways. The GS analysis revealed enriched themes such as energy metabolism, cell proliferation/growth/survival, muscle adaptations, and cytokine–cytokine interaction, all of which have been previously proposed as HIIT responses. Moreover, related cell signaling pathways were also measured. Specifically, G‐protein‐mediated signal transduction, phosphatidylinositide 3‐kinases (PI3K) – protein kinase B (PKB) and Janus kinase (JAK) – Signal Transducer and Activator of Transcription (STAT) signaling cascades were over‐represented. Additionally, the RNA‐Seq analysis also identified several HIIT‐responsive microRNAs (miRNAs) that were involved in regulating hair follicle‐specific processes, such as miR‐99a. For the first time, this study demonstrated that both existing and new biomarkers like miRNA can be explored for HIIT using the transcriptomic responses exhibited by the hair follicle.
We propose scalp hair follicle as a minimally invasive yet comprehensive biomarker discovery system to effectively characterize and monitor HIIT‐induced cellular and molecular responses. For the first time, this study demonstrated that both existing and new biomarkers like miRNA could be explored for HIIT using the transcriptomic responses exhibited by the hair follicle, providing a foundation for additional HIIT evaluation measures.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>Adaptation</subject><subject>Adaptation, Physiological</subject><subject>Adult</subject><subject>AKT protein</subject><subject>Biomarkers - metabolism</subject><subject>Cell proliferation</subject><subject>Cell survival</subject><subject>Cytokines</subject><subject>Endurance training</subject><subject>Energy metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Profiling - methods</subject><subject>Hair</subject><subject>Hair Follicle - metabolism</subject><subject>High-Intensity Interval Training</subject><subject>Humans</subject><subject>Janus kinase</subject><subject>Janus Kinases - genetics</subject><subject>Janus Kinases - metabolism</subject><subject>Kinases</subject><subject>Male</subject><subject>miRNA</subject><subject>Molecular Diagnostic Techniques - methods</subject><subject>muscle contraction</subject><subject>Original Research</subject><subject>Phosphatidylinositol 3-Kinases - genetics</subject><subject>Phosphatidylinositol 3-Kinases - metabolism</subject><subject>Physical fitness</subject><subject>Physical training</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins c-akt - genetics</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Receptors, G-Protein-Coupled - genetics</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>RNA‐Seq</subject><subject>Signal Transduction</subject><subject>STAT Transcription Factors - genetics</subject><subject>STAT Transcription Factors - metabolism</subject><subject>Transcription</subject><subject>Transcriptome</subject><issn>2051-817X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk9rFDEYhwdBbGl78i4BL4Juzd_JxINQinULBT0o6Cm8k83sZskkYzKzZW9-BD-An85PYna3FuvBS0KSh-d98_KrqqcEnxPeEP56WG3pOWGC8UfVMcWCzBoivxxVZzmvMcYEM6Ywf1IdUUUJbYQ6rn7Opx4CWoFLqIveO-MtGhOEbJIbxthbNKTYOe_C8g0C1LvgevB-i1zYQHabQsfoy4IgZ5sz6qO3ZvKQECxgGGF0MWQ0DTEgH29_ff-xiX7q7Su0cstVObow2pDduDOONm3A7-qXMmF5Wj3uwGd7drefVJ-v3n26nM9uPry_vry4mRlBGj5roRUSK0OsoYoDBalkqxTrqKgBMzAgbYc7IzCGBhipLcFdixctZorVZSon1fXBu4iw1kMqP0xbHcHp_UVMSw1p3I1GS95KKcqEqWk5N7ZpOgzciJpzUhNeF9fbg2uY2t4ujA3lN_6B9OFLcCu9jBstJJW04UXw4k6Q4rfJ5lH3LhvrPQQbp6yJkhwThmta0Of_oOs4pVBGtaNEw1QJQaFeHiiTYs7JdvfNEKz3wdG74Oh9cAr97O_-79k_kSkAPQC3ztvt_1z64_wrPVh_A1d_1ac</recordid><startdate>201712</startdate><enddate>201712</enddate><creator>Zhang, Jing</creator><creator>Wallace, Sarah J.</creator><creator>Shiu, Maria Y.</creator><creator>Smith, Ingrid</creator><creator>Rhind, Shawn G.</creator><creator>Langlois, Valerie S.</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</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>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>201712</creationdate><title>Human hair follicle transcriptome profiling: a minimally invasive tool to assess molecular adaptations upon low‐volume, high‐intensity interval training</title><author>Zhang, Jing ; Wallace, Sarah J. ; Shiu, Maria Y. ; Smith, Ingrid ; Rhind, Shawn G. ; Langlois, Valerie S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5184-bab5709c1ec294a2a797b993f256a03aca7ef0fc500a8a316e10fb0db03936103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>Adaptation</topic><topic>Adaptation, Physiological</topic><topic>Adult</topic><topic>AKT protein</topic><topic>Biomarkers - metabolism</topic><topic>Cell proliferation</topic><topic>Cell survival</topic><topic>Cytokines</topic><topic>Endurance training</topic><topic>Energy metabolism</topic><topic>Gene expression</topic><topic>Gene Expression Profiling - methods</topic><topic>Hair</topic><topic>Hair Follicle - metabolism</topic><topic>High-Intensity Interval Training</topic><topic>Humans</topic><topic>Janus kinase</topic><topic>Janus Kinases - genetics</topic><topic>Janus Kinases - metabolism</topic><topic>Kinases</topic><topic>Male</topic><topic>miRNA</topic><topic>Molecular Diagnostic Techniques - methods</topic><topic>muscle contraction</topic><topic>Original Research</topic><topic>Phosphatidylinositol 3-Kinases - genetics</topic><topic>Phosphatidylinositol 3-Kinases - metabolism</topic><topic>Physical fitness</topic><topic>Physical training</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Proto-Oncogene Proteins c-akt - genetics</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Receptors, G-Protein-Coupled - genetics</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>RNA‐Seq</topic><topic>Signal Transduction</topic><topic>STAT Transcription Factors - genetics</topic><topic>STAT Transcription Factors - metabolism</topic><topic>Transcription</topic><topic>Transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Jing</creatorcontrib><creatorcontrib>Wallace, Sarah J.</creatorcontrib><creatorcontrib>Shiu, Maria Y.</creatorcontrib><creatorcontrib>Smith, Ingrid</creatorcontrib><creatorcontrib>Rhind, Shawn G.</creatorcontrib><creatorcontrib>Langlois, Valerie S.</creatorcontrib><collection>Wiley-Blackwell Open Access Titles(OpenAccess)</collection><collection>Wiley-Blackwell Open Access Backfiles</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech 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>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Physiological reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Jing</au><au>Wallace, Sarah J.</au><au>Shiu, Maria Y.</au><au>Smith, Ingrid</au><au>Rhind, Shawn G.</au><au>Langlois, Valerie S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human hair follicle transcriptome profiling: a minimally invasive tool to assess molecular adaptations upon low‐volume, high‐intensity interval training</atitle><jtitle>Physiological reports</jtitle><addtitle>Physiol Rep</addtitle><date>2017-12</date><risdate>2017</risdate><volume>5</volume><issue>23</issue><epage>n/a</epage><eissn>2051-817X</eissn><abstract>High‐intensity interval training (HIIT) has become a popular fitness training approach under both civilian and military settings. Consisting of brief and intense exercise intervals, HIIT requires less time commitment yet is able to produce the consistent targeted physical adaptations as conventional endurance training. To effectively characterize and monitor HIIT‐induced cellular and molecular responses, a highly accessible yet comprehensive biomarker discovery source is desirable. Both gene differential expression (DE) and gene set (GS) analyses were conducted using hair follicle transcriptome established from pre and postexercise subjects upon a 10‐day HIIT program by RNA‐Seq, Comparing between pre and posttraining groups, differentially expressed protein coding genes were identified. To interpret the functional significance of the DE results, a comprehensive GS analysis approach featuring multiple algorithms was used to enrich gene ontology (GO) terms and KEGG pathways. The GS analysis revealed enriched themes such as energy metabolism, cell proliferation/growth/survival, muscle adaptations, and cytokine–cytokine interaction, all of which have been previously proposed as HIIT responses. Moreover, related cell signaling pathways were also measured. Specifically, G‐protein‐mediated signal transduction, phosphatidylinositide 3‐kinases (PI3K) – protein kinase B (PKB) and Janus kinase (JAK) – Signal Transducer and Activator of Transcription (STAT) signaling cascades were over‐represented. Additionally, the RNA‐Seq analysis also identified several HIIT‐responsive microRNAs (miRNAs) that were involved in regulating hair follicle‐specific processes, such as miR‐99a. For the first time, this study demonstrated that both existing and new biomarkers like miRNA can be explored for HIIT using the transcriptomic responses exhibited by the hair follicle.
We propose scalp hair follicle as a minimally invasive yet comprehensive biomarker discovery system to effectively characterize and monitor HIIT‐induced cellular and molecular responses. For the first time, this study demonstrated that both existing and new biomarkers like miRNA could be explored for HIIT using the transcriptomic responses exhibited by the hair follicle, providing a foundation for additional HIIT evaluation measures.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>29212859</pmid><doi>10.14814/phy2.13534</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase Adaptation Adaptation, Physiological Adult AKT protein Biomarkers - metabolism Cell proliferation Cell survival Cytokines Endurance training Energy metabolism Gene expression Gene Expression Profiling - methods Hair Hair Follicle - metabolism High-Intensity Interval Training Humans Janus kinase Janus Kinases - genetics Janus Kinases - metabolism Kinases Male miRNA Molecular Diagnostic Techniques - methods muscle contraction Original Research Phosphatidylinositol 3-Kinases - genetics Phosphatidylinositol 3-Kinases - metabolism Physical fitness Physical training Physiology Proteins Proto-Oncogene Proteins c-akt - genetics Proto-Oncogene Proteins c-akt - metabolism Receptors, G-Protein-Coupled - genetics Receptors, G-Protein-Coupled - metabolism RNA‐Seq Signal Transduction STAT Transcription Factors - genetics STAT Transcription Factors - metabolism Transcription Transcriptome |
title | Human hair follicle transcriptome profiling: a minimally invasive tool to assess molecular adaptations upon low‐volume, high‐intensity interval training |
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