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Molecular cartography of the human skin surface in 3D
Significance The paper describes the implementation of an approach to study the chemical makeup of human skin surface and correlate it to the microbes that live in the skin. We provide the translation of molecular information in high-spatial resolution 3D to understand the body distribution of skin...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2015-04, Vol.112 (17), p.E2120-E2129 |
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creator | Bouslimani, Amina Porto, Carla Rath, Christopher M. Wang, Mingxun Guo, Yurong Gonzalez, Antonio Berg-Lyon, Donna Ackermann, Gail Christensen, Gitte Julie Moeller Nakatsuji, Teruaki Zhang, Lingjuan Borkowski, Andrew W. Meehan, Michael J. Dorrestein, Kathleen Gallo, Richard L. Bandeira, Nuno Knight, Rob Alexandrov, Theodore Dorrestein, Pieter C. |
description | Significance The paper describes the implementation of an approach to study the chemical makeup of human skin surface and correlate it to the microbes that live in the skin. We provide the translation of molecular information in high-spatial resolution 3D to understand the body distribution of skin molecules and bacteria. In addition, we use integrative analysis to interpret, at a molecular level, the large scale of data obtained from human skin samples. Correlations between molecules and microbes can be obtained to further gain insights into the chemical milieu in which these different microbial communities live.
The human skin is an organ with a surface area of 1.5–2 m ² that provides our interface with the environment. The molecular composition of this organ is derived from host cells, microbiota, and external molecules. The chemical makeup of the skin surface is largely undefined. Here we advance the technologies needed to explore the topographical distribution of skin molecules, using 3D mapping of mass spectrometry data and microbial 16S rRNA amplicon sequences. Our 3D maps reveal that the molecular composition of skin has diverse distributions and that the composition is defined not only by skin cells and microbes but also by our daily routines, including the application of hygiene products. The technological development of these maps lays a foundation for studying the spatial relationships of human skin with hygiene, the microbiota, and environment, with potential for developing predictive models of skin phenotypes tailored to individual health. |
doi_str_mv | 10.1073/pnas.1424409112 |
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The human skin is an organ with a surface area of 1.5–2 m ² that provides our interface with the environment. The molecular composition of this organ is derived from host cells, microbiota, and external molecules. The chemical makeup of the skin surface is largely undefined. Here we advance the technologies needed to explore the topographical distribution of skin molecules, using 3D mapping of mass spectrometry data and microbial 16S rRNA amplicon sequences. Our 3D maps reveal that the molecular composition of skin has diverse distributions and that the composition is defined not only by skin cells and microbes but also by our daily routines, including the application of hygiene products. The technological development of these maps lays a foundation for studying the spatial relationships of human skin with hygiene, the microbiota, and environment, with potential for developing predictive models of skin phenotypes tailored to individual health.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1424409112</identifier><identifier>PMID: 25825778</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Adult ; Biological Sciences ; Cartography ; Female ; Humans ; Imaging, Three-Dimensional ; Male ; Mapping ; Mass Spectrometry ; Microbiota - physiology ; Models, Biological ; Molecules ; PNAS Plus ; RNA, Bacterial - genetics ; RNA, Bacterial - metabolism ; RNA, Ribosomal, 16S - genetics ; RNA, Ribosomal, 16S - metabolism ; Skin ; Skin - microbiology ; Three dimensional imaging</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2015-04, Vol.112 (17), p.E2120-E2129</ispartof><rights>Volumes 1–89 and 106–112, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences Apr 28, 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c591t-add4735a637c440d75285a2f4821daf7be00b8023f850167bf748f8d37e23e393</citedby><cites>FETCH-LOGICAL-c591t-add4735a637c440d75285a2f4821daf7be00b8023f850167bf748f8d37e23e393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/112/17.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26462598$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26462598$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25825778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bouslimani, Amina</creatorcontrib><creatorcontrib>Porto, Carla</creatorcontrib><creatorcontrib>Rath, Christopher M.</creatorcontrib><creatorcontrib>Wang, Mingxun</creatorcontrib><creatorcontrib>Guo, Yurong</creatorcontrib><creatorcontrib>Gonzalez, Antonio</creatorcontrib><creatorcontrib>Berg-Lyon, Donna</creatorcontrib><creatorcontrib>Ackermann, Gail</creatorcontrib><creatorcontrib>Christensen, Gitte Julie Moeller</creatorcontrib><creatorcontrib>Nakatsuji, Teruaki</creatorcontrib><creatorcontrib>Zhang, Lingjuan</creatorcontrib><creatorcontrib>Borkowski, Andrew W.</creatorcontrib><creatorcontrib>Meehan, Michael J.</creatorcontrib><creatorcontrib>Dorrestein, Kathleen</creatorcontrib><creatorcontrib>Gallo, Richard L.</creatorcontrib><creatorcontrib>Bandeira, Nuno</creatorcontrib><creatorcontrib>Knight, Rob</creatorcontrib><creatorcontrib>Alexandrov, Theodore</creatorcontrib><creatorcontrib>Dorrestein, Pieter C.</creatorcontrib><title>Molecular cartography of the human skin surface in 3D</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Significance The paper describes the implementation of an approach to study the chemical makeup of human skin surface and correlate it to the microbes that live in the skin. We provide the translation of molecular information in high-spatial resolution 3D to understand the body distribution of skin molecules and bacteria. In addition, we use integrative analysis to interpret, at a molecular level, the large scale of data obtained from human skin samples. Correlations between molecules and microbes can be obtained to further gain insights into the chemical milieu in which these different microbial communities live.
The human skin is an organ with a surface area of 1.5–2 m ² that provides our interface with the environment. The molecular composition of this organ is derived from host cells, microbiota, and external molecules. The chemical makeup of the skin surface is largely undefined. Here we advance the technologies needed to explore the topographical distribution of skin molecules, using 3D mapping of mass spectrometry data and microbial 16S rRNA amplicon sequences. Our 3D maps reveal that the molecular composition of skin has diverse distributions and that the composition is defined not only by skin cells and microbes but also by our daily routines, including the application of hygiene products. The technological development of these maps lays a foundation for studying the spatial relationships of human skin with hygiene, the microbiota, and environment, with potential for developing predictive models of skin phenotypes tailored to individual health.</description><subject>Adult</subject><subject>Biological Sciences</subject><subject>Cartography</subject><subject>Female</subject><subject>Humans</subject><subject>Imaging, Three-Dimensional</subject><subject>Male</subject><subject>Mapping</subject><subject>Mass Spectrometry</subject><subject>Microbiota - physiology</subject><subject>Models, Biological</subject><subject>Molecules</subject><subject>PNAS Plus</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Bacterial - metabolism</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>RNA, Ribosomal, 16S - metabolism</subject><subject>Skin</subject><subject>Skin - microbiology</subject><subject>Three dimensional imaging</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkc1v1DAQxS0EokvhzAmIxIVLWnv8MfYFCZVSkIo4QM-WN7F3s2TjrZ0g9b-vo122wImLPdL7zdPMPEJeMnrGKPLz3eDyGRMgBDWMwSOyYKWolTD0MVlQCljrop6QZzlvKKVGavqUnIDUIBH1gsivsffN1LtUNS6NcZXcbn1XxVCNa1-tp60bqvyzK8-Ugmt8VUr-8Tl5Elyf_YvDf0puPl3-uPhcX3-7-nLx4bpupGFj7dpWIJdOcWzKhC1K0NJBEBpY6wIuPaVLTYEHLSlTuAwodNAtRw_cc8NPyfu9725abn3b-GFMrre71G1durPRdfZvZejWdhV_WSGY1lIVg3cHgxRvJ59Hu-1y4_veDT5O2TKlUSEo_B8UkSMarQv69h90E6c0lEvMhmUfAJip8z3VpJhz8uE4N6N2Ts_O6dmH9ErH6z_XPfK_4ypAdQDmzqMdA8vQXgIDWpBXe2STx5geLJRQIM1s8WavBxetW6Uu25vvUK5PKeMGjOT3Noiw2A</recordid><startdate>20150428</startdate><enddate>20150428</enddate><creator>Bouslimani, Amina</creator><creator>Porto, Carla</creator><creator>Rath, Christopher M.</creator><creator>Wang, Mingxun</creator><creator>Guo, Yurong</creator><creator>Gonzalez, Antonio</creator><creator>Berg-Lyon, Donna</creator><creator>Ackermann, Gail</creator><creator>Christensen, Gitte Julie Moeller</creator><creator>Nakatsuji, Teruaki</creator><creator>Zhang, Lingjuan</creator><creator>Borkowski, Andrew W.</creator><creator>Meehan, Michael J.</creator><creator>Dorrestein, Kathleen</creator><creator>Gallo, Richard L.</creator><creator>Bandeira, Nuno</creator><creator>Knight, Rob</creator><creator>Alexandrov, Theodore</creator><creator>Dorrestein, Pieter C.</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7ST</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20150428</creationdate><title>Molecular cartography of the human skin surface in 3D</title><author>Bouslimani, Amina ; Porto, Carla ; Rath, Christopher M. ; Wang, Mingxun ; Guo, Yurong ; Gonzalez, Antonio ; Berg-Lyon, Donna ; Ackermann, Gail ; Christensen, Gitte Julie Moeller ; Nakatsuji, Teruaki ; Zhang, Lingjuan ; Borkowski, Andrew W. ; Meehan, Michael J. ; Dorrestein, Kathleen ; Gallo, Richard L. ; Bandeira, Nuno ; Knight, Rob ; Alexandrov, Theodore ; Dorrestein, Pieter C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c591t-add4735a637c440d75285a2f4821daf7be00b8023f850167bf748f8d37e23e393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Biological Sciences</topic><topic>Cartography</topic><topic>Female</topic><topic>Humans</topic><topic>Imaging, Three-Dimensional</topic><topic>Male</topic><topic>Mapping</topic><topic>Mass Spectrometry</topic><topic>Microbiota - 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PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2015-04-28</date><risdate>2015</risdate><volume>112</volume><issue>17</issue><spage>E2120</spage><epage>E2129</epage><pages>E2120-E2129</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Significance The paper describes the implementation of an approach to study the chemical makeup of human skin surface and correlate it to the microbes that live in the skin. We provide the translation of molecular information in high-spatial resolution 3D to understand the body distribution of skin molecules and bacteria. In addition, we use integrative analysis to interpret, at a molecular level, the large scale of data obtained from human skin samples. Correlations between molecules and microbes can be obtained to further gain insights into the chemical milieu in which these different microbial communities live.
The human skin is an organ with a surface area of 1.5–2 m ² that provides our interface with the environment. The molecular composition of this organ is derived from host cells, microbiota, and external molecules. The chemical makeup of the skin surface is largely undefined. Here we advance the technologies needed to explore the topographical distribution of skin molecules, using 3D mapping of mass spectrometry data and microbial 16S rRNA amplicon sequences. Our 3D maps reveal that the molecular composition of skin has diverse distributions and that the composition is defined not only by skin cells and microbes but also by our daily routines, including the application of hygiene products. The technological development of these maps lays a foundation for studying the spatial relationships of human skin with hygiene, the microbiota, and environment, with potential for developing predictive models of skin phenotypes tailored to individual health.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>25825778</pmid><doi>10.1073/pnas.1424409112</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological Sciences Cartography Female Humans Imaging, Three-Dimensional Male Mapping Mass Spectrometry Microbiota - physiology Models, Biological Molecules PNAS Plus RNA, Bacterial - genetics RNA, Bacterial - metabolism RNA, Ribosomal, 16S - genetics RNA, Ribosomal, 16S - metabolism Skin Skin - microbiology Three dimensional imaging |
title | Molecular cartography of the human skin surface in 3D |
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