Defining the Design Principles of Skin Epidermis Postnatal Growth
During embryonic and postnatal development, organs and tissues grow steadily to achieve their final size at the end of puberty. However, little is known about the cellular dynamics that mediate postnatal growth. By combining in vivo clonal lineage tracing, proliferation kinetics, single-cell transcr...
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creator | Dekoninck, Sophie Hannezo, Edouard Sifrim, Alejandro Miroshnikova, Yekaterina A. Aragona, Mariaceleste Malfait, Milan Gargouri, Souhir de Neunheuser, Charlotte Dubois, Christine Voet, Thierry Wickström, Sara A. Simons, Benjamin D. Blanpain, Cédric |
description | During embryonic and postnatal development, organs and tissues grow steadily to achieve their final size at the end of puberty. However, little is known about the cellular dynamics that mediate postnatal growth. By combining in vivo clonal lineage tracing, proliferation kinetics, single-cell transcriptomics, and in vitro micro-pattern experiments, we resolved the cellular dynamics taking place during postnatal skin epidermis expansion. Our data revealed that harmonious growth is engineered by a single population of developmental progenitors presenting a fixed fate imbalance of self-renewing divisions with an ever-decreasing proliferation rate. Single-cell RNA sequencing revealed that epidermal developmental progenitors form a more uniform population compared with adult stem and progenitor cells. Finally, we found that the spatial pattern of cell division orientation is dictated locally by the underlying collagen fiber orientation. Our results uncover a simple design principle of organ growth where progenitors and differentiated cells expand in harmony with their surrounding tissues.
[Display omitted]
•Linear growth of the epidermis during postnatal development•Constant imbalance of self-renewal and decreasing proliferation leads to IFE growth•Higher molecular homogeneity in developmental progenitors•Orientation of clonal growth follows orientation of collagen fibers
During postnatal growth, tissues steadily grow until they achieve their final size. Looking at the interfollicular epidermis in mice, Dekoninck et al. find that progenitors present an excess of self-renewing division throughout the development. This imbalance, coupled with an ever-decreasing proliferation rate in both scale and interscale compartments, provides linear tissue expansion and maintenance of skin barrier function at the same time. |
doi_str_mv | 10.1016/j.cell.2020.03.015 |
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[Display omitted]
•Linear growth of the epidermis during postnatal development•Constant imbalance of self-renewal and decreasing proliferation leads to IFE growth•Higher molecular homogeneity in developmental progenitors•Orientation of clonal growth follows orientation of collagen fibers
During postnatal growth, tissues steadily grow until they achieve their final size. Looking at the interfollicular epidermis in mice, Dekoninck et al. find that progenitors present an excess of self-renewing division throughout the development. This imbalance, coupled with an ever-decreasing proliferation rate in both scale and interscale compartments, provides linear tissue expansion and maintenance of skin barrier function at the same time.</description><identifier>ISSN: 0092-8674</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/j.cell.2020.03.015</identifier><identifier>PMID: 32259486</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>adults ; Animals ; Animals, Outbred Strains ; Cell Differentiation - physiology ; cell division ; Cell Division - physiology ; Cell Lineage - genetics ; Cell Proliferation - physiology ; Cells, Cultured ; collagen ; development ; differentiation ; Epidermal Cells - metabolism ; Epidermal Cells - pathology ; epidermis ; Epidermis - growth & development ; Epidermis - metabolism ; Female ; growth ; imbalance ; Male ; Mice ; Mice, Transgenic ; postnatal ; postnatal development ; progenitors ; puberty ; self-renewal ; sequence analysis ; skin ; Skin - growth & development ; stem cells ; Stem Cells - cytology ; transcriptomics</subject><ispartof>Cell, 2020-04, Vol.181 (3), p.604-620.e22</ispartof><rights>2020</rights><rights>Crown Copyright © 2020. Published by Elsevier Inc. All rights reserved.</rights><rights>Crown Copyright © 2020 Published by Elsevier Inc. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-a32df98a65ad94c68e27e32053d6a885c08f0c8e30df9314a1919b2ca9571d293</citedby><cites>FETCH-LOGICAL-c488t-a32df98a65ad94c68e27e32053d6a885c08f0c8e30df9314a1919b2ca9571d293</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0092867420302774$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32259486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dekoninck, Sophie</creatorcontrib><creatorcontrib>Hannezo, Edouard</creatorcontrib><creatorcontrib>Sifrim, Alejandro</creatorcontrib><creatorcontrib>Miroshnikova, Yekaterina A.</creatorcontrib><creatorcontrib>Aragona, Mariaceleste</creatorcontrib><creatorcontrib>Malfait, Milan</creatorcontrib><creatorcontrib>Gargouri, Souhir</creatorcontrib><creatorcontrib>de Neunheuser, Charlotte</creatorcontrib><creatorcontrib>Dubois, Christine</creatorcontrib><creatorcontrib>Voet, Thierry</creatorcontrib><creatorcontrib>Wickström, Sara A.</creatorcontrib><creatorcontrib>Simons, Benjamin D.</creatorcontrib><creatorcontrib>Blanpain, Cédric</creatorcontrib><title>Defining the Design Principles of Skin Epidermis Postnatal Growth</title><title>Cell</title><addtitle>Cell</addtitle><description>During embryonic and postnatal development, organs and tissues grow steadily to achieve their final size at the end of puberty. However, little is known about the cellular dynamics that mediate postnatal growth. By combining in vivo clonal lineage tracing, proliferation kinetics, single-cell transcriptomics, and in vitro micro-pattern experiments, we resolved the cellular dynamics taking place during postnatal skin epidermis expansion. Our data revealed that harmonious growth is engineered by a single population of developmental progenitors presenting a fixed fate imbalance of self-renewing divisions with an ever-decreasing proliferation rate. Single-cell RNA sequencing revealed that epidermal developmental progenitors form a more uniform population compared with adult stem and progenitor cells. Finally, we found that the spatial pattern of cell division orientation is dictated locally by the underlying collagen fiber orientation. Our results uncover a simple design principle of organ growth where progenitors and differentiated cells expand in harmony with their surrounding tissues.
[Display omitted]
•Linear growth of the epidermis during postnatal development•Constant imbalance of self-renewal and decreasing proliferation leads to IFE growth•Higher molecular homogeneity in developmental progenitors•Orientation of clonal growth follows orientation of collagen fibers
During postnatal growth, tissues steadily grow until they achieve their final size. Looking at the interfollicular epidermis in mice, Dekoninck et al. find that progenitors present an excess of self-renewing division throughout the development. This imbalance, coupled with an ever-decreasing proliferation rate in both scale and interscale compartments, provides linear tissue expansion and maintenance of skin barrier function at the same time.</description><subject>adults</subject><subject>Animals</subject><subject>Animals, Outbred Strains</subject><subject>Cell Differentiation - physiology</subject><subject>cell division</subject><subject>Cell Division - physiology</subject><subject>Cell Lineage - genetics</subject><subject>Cell Proliferation - physiology</subject><subject>Cells, Cultured</subject><subject>collagen</subject><subject>development</subject><subject>differentiation</subject><subject>Epidermal Cells - metabolism</subject><subject>Epidermal Cells - pathology</subject><subject>epidermis</subject><subject>Epidermis - growth & development</subject><subject>Epidermis - metabolism</subject><subject>Female</subject><subject>growth</subject><subject>imbalance</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>postnatal</subject><subject>postnatal development</subject><subject>progenitors</subject><subject>puberty</subject><subject>self-renewal</subject><subject>sequence analysis</subject><subject>skin</subject><subject>Skin - growth & development</subject><subject>stem cells</subject><subject>Stem Cells - cytology</subject><subject>transcriptomics</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1P3DAQxa0KVBbaf6CHKkcuCeOvxJZQJbR8SkhFanu2jDPZ9ZK1t3YWxH9PoqWovZTTHOb3nmbeI-QLhYoCrU9WlcO-rxgwqIBXQOUHMqOgm1LQhu2RGYBmpaobcUAOc14BgJJSfiQHnDGphapn5OwcOx98WBTDEotzzH4Rirvkg_ObHnMRu-LHgw_Fxca3mNY-F3cxD8EOti-uUnwalp_Ifmf7jJ9f5xH5dXnxc35d3n6_upmf3ZZOKDWUlrO208rW0rZauFoha5AzkLytrVLSgerAKeQwYpwKSzXV98xZLRvaMs2PyLed72Z7v8bWYRiS7c0m-bVNzyZab_7dBL80i_hoGqqVbiaD41eDFH9vMQ9mfGdK0AaM22yY4JorIQR_H-WqqWvGpRhRtkNdijkn7N4uomCmmszKTEoz1WSAm7GmUfT171_eJH96GYHTHYBjoo8ek8nOY3DY-oRuMG30__N_Aa6Oo3M</recordid><startdate>20200430</startdate><enddate>20200430</enddate><creator>Dekoninck, Sophie</creator><creator>Hannezo, Edouard</creator><creator>Sifrim, Alejandro</creator><creator>Miroshnikova, Yekaterina A.</creator><creator>Aragona, Mariaceleste</creator><creator>Malfait, Milan</creator><creator>Gargouri, Souhir</creator><creator>de Neunheuser, Charlotte</creator><creator>Dubois, Christine</creator><creator>Voet, Thierry</creator><creator>Wickström, Sara A.</creator><creator>Simons, Benjamin D.</creator><creator>Blanpain, Cédric</creator><general>Elsevier Inc</general><general>Cell Press</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>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20200430</creationdate><title>Defining the Design Principles of Skin Epidermis Postnatal Growth</title><author>Dekoninck, Sophie ; Hannezo, Edouard ; Sifrim, Alejandro ; Miroshnikova, Yekaterina A. ; Aragona, Mariaceleste ; Malfait, Milan ; Gargouri, Souhir ; de Neunheuser, Charlotte ; Dubois, Christine ; Voet, Thierry ; Wickström, Sara A. ; Simons, Benjamin D. ; Blanpain, Cédric</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-a32df98a65ad94c68e27e32053d6a885c08f0c8e30df9314a1919b2ca9571d293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>adults</topic><topic>Animals</topic><topic>Animals, Outbred Strains</topic><topic>Cell Differentiation - physiology</topic><topic>cell division</topic><topic>Cell Division - physiology</topic><topic>Cell Lineage - genetics</topic><topic>Cell Proliferation - physiology</topic><topic>Cells, Cultured</topic><topic>collagen</topic><topic>development</topic><topic>differentiation</topic><topic>Epidermal Cells - metabolism</topic><topic>Epidermal Cells - pathology</topic><topic>epidermis</topic><topic>Epidermis - growth & development</topic><topic>Epidermis - metabolism</topic><topic>Female</topic><topic>growth</topic><topic>imbalance</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>postnatal</topic><topic>postnatal development</topic><topic>progenitors</topic><topic>puberty</topic><topic>self-renewal</topic><topic>sequence analysis</topic><topic>skin</topic><topic>Skin - growth & development</topic><topic>stem cells</topic><topic>Stem Cells - cytology</topic><topic>transcriptomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dekoninck, Sophie</creatorcontrib><creatorcontrib>Hannezo, Edouard</creatorcontrib><creatorcontrib>Sifrim, Alejandro</creatorcontrib><creatorcontrib>Miroshnikova, Yekaterina A.</creatorcontrib><creatorcontrib>Aragona, Mariaceleste</creatorcontrib><creatorcontrib>Malfait, Milan</creatorcontrib><creatorcontrib>Gargouri, Souhir</creatorcontrib><creatorcontrib>de Neunheuser, Charlotte</creatorcontrib><creatorcontrib>Dubois, Christine</creatorcontrib><creatorcontrib>Voet, Thierry</creatorcontrib><creatorcontrib>Wickström, Sara A.</creatorcontrib><creatorcontrib>Simons, Benjamin D.</creatorcontrib><creatorcontrib>Blanpain, Cédric</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>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dekoninck, Sophie</au><au>Hannezo, Edouard</au><au>Sifrim, Alejandro</au><au>Miroshnikova, Yekaterina A.</au><au>Aragona, Mariaceleste</au><au>Malfait, Milan</au><au>Gargouri, Souhir</au><au>de Neunheuser, Charlotte</au><au>Dubois, Christine</au><au>Voet, Thierry</au><au>Wickström, Sara A.</au><au>Simons, Benjamin D.</au><au>Blanpain, Cédric</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defining the Design Principles of Skin Epidermis Postnatal Growth</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>2020-04-30</date><risdate>2020</risdate><volume>181</volume><issue>3</issue><spage>604</spage><epage>620.e22</epage><pages>604-620.e22</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><abstract>During embryonic and postnatal development, organs and tissues grow steadily to achieve their final size at the end of puberty. However, little is known about the cellular dynamics that mediate postnatal growth. By combining in vivo clonal lineage tracing, proliferation kinetics, single-cell transcriptomics, and in vitro micro-pattern experiments, we resolved the cellular dynamics taking place during postnatal skin epidermis expansion. Our data revealed that harmonious growth is engineered by a single population of developmental progenitors presenting a fixed fate imbalance of self-renewing divisions with an ever-decreasing proliferation rate. Single-cell RNA sequencing revealed that epidermal developmental progenitors form a more uniform population compared with adult stem and progenitor cells. Finally, we found that the spatial pattern of cell division orientation is dictated locally by the underlying collagen fiber orientation. Our results uncover a simple design principle of organ growth where progenitors and differentiated cells expand in harmony with their surrounding tissues.
[Display omitted]
•Linear growth of the epidermis during postnatal development•Constant imbalance of self-renewal and decreasing proliferation leads to IFE growth•Higher molecular homogeneity in developmental progenitors•Orientation of clonal growth follows orientation of collagen fibers
During postnatal growth, tissues steadily grow until they achieve their final size. Looking at the interfollicular epidermis in mice, Dekoninck et al. find that progenitors present an excess of self-renewing division throughout the development. This imbalance, coupled with an ever-decreasing proliferation rate in both scale and interscale compartments, provides linear tissue expansion and maintenance of skin barrier function at the same time.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32259486</pmid><doi>10.1016/j.cell.2020.03.015</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
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subjects | adults Animals Animals, Outbred Strains Cell Differentiation - physiology cell division Cell Division - physiology Cell Lineage - genetics Cell Proliferation - physiology Cells, Cultured collagen development differentiation Epidermal Cells - metabolism Epidermal Cells - pathology epidermis Epidermis - growth & development Epidermis - metabolism Female growth imbalance Male Mice Mice, Transgenic postnatal postnatal development progenitors puberty self-renewal sequence analysis skin Skin - growth & development stem cells Stem Cells - cytology transcriptomics |
title | Defining the Design Principles of Skin Epidermis Postnatal Growth |
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