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Dedifferentiation maintains melanocyte stem cells in a dynamic niche
For unknow reasons, the melanocyte stem cell (McSC) system fails earlier than other adult stem cell populations 1 , which leads to hair greying in most humans and mice 2 , 3 . Current dogma states that McSCs are reserved in an undifferentiated state in the hair follicle niche, physically segregated...
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Published in: | Nature (London) 2023-04, Vol.616 (7958), p.774-782 |
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creator | Sun, Qi Lee, Wendy Hu, Hai Ogawa, Tatsuya De Leon, Sophie Katehis, Ioanna Lim, Chae Ho Takeo, Makoto Cammer, Michael Taketo, M. Mark Gay, Denise L. Millar, Sarah E. Ito, Mayumi |
description | For unknow reasons, the melanocyte stem cell (McSC) system fails earlier than other adult stem cell populations
1
, which leads to hair greying in most humans and mice
2
,
3
. Current dogma states that McSCs are reserved in an undifferentiated state in the hair follicle niche, physically segregated from differentiated progeny that migrate away following cues of regenerative stimuli
4
–
8
. Here we show that most McSCs toggle between transit-amplifying and stem cell states for both self-renewal and generation of mature progeny, a mechanism fundamentally distinct from those of other self-renewing systems. Live imaging and single-cell RNA sequencing revealed that McSCs are mobile, translocating between hair follicle stem cell and transit-amplifying compartments where they reversibly enter distinct differentiation states governed by local microenvironmental cues (for example, WNT). Long-term lineage tracing demonstrated that the McSC system is maintained by reverted McSCs rather than by reserved stem cells inherently exempt from reversible changes. During ageing, there is accumulation of stranded McSCs that do not contribute to the regeneration of melanocyte progeny. These results identify a new model whereby dedifferentiation is integral to homeostatic stem cell maintenance and suggest that modulating McSC mobility may represent a new approach for the prevention of hair greying.
Local microenvironmental cues modulate melanocyte stem cells, which control hair pigmentation, to enter different differentiation states, shifting between hair follicle stem cell and transit-amplifying compartments, a process that is different to other self-renewing systems. |
doi_str_mv | 10.1038/s41586-023-05960-6 |
format | article |
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1
, which leads to hair greying in most humans and mice
2
,
3
. Current dogma states that McSCs are reserved in an undifferentiated state in the hair follicle niche, physically segregated from differentiated progeny that migrate away following cues of regenerative stimuli
4
–
8
. Here we show that most McSCs toggle between transit-amplifying and stem cell states for both self-renewal and generation of mature progeny, a mechanism fundamentally distinct from those of other self-renewing systems. Live imaging and single-cell RNA sequencing revealed that McSCs are mobile, translocating between hair follicle stem cell and transit-amplifying compartments where they reversibly enter distinct differentiation states governed by local microenvironmental cues (for example, WNT). Long-term lineage tracing demonstrated that the McSC system is maintained by reverted McSCs rather than by reserved stem cells inherently exempt from reversible changes. During ageing, there is accumulation of stranded McSCs that do not contribute to the regeneration of melanocyte progeny. These results identify a new model whereby dedifferentiation is integral to homeostatic stem cell maintenance and suggest that modulating McSC mobility may represent a new approach for the prevention of hair greying.
Local microenvironmental cues modulate melanocyte stem cells, which control hair pigmentation, to enter different differentiation states, shifting between hair follicle stem cell and transit-amplifying compartments, a process that is different to other self-renewing systems.</description><identifier>ISSN: 0028-0836</identifier><identifier>ISSN: 1476-4687</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/s41586-023-05960-6</identifier><identifier>PMID: 37076619</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 13/51 ; 14 ; 14/1 ; 14/19 ; 14/32 ; 14/63 ; 14/69 ; 45/91 ; 631/532/2118/2438 ; 631/532/7 ; 64 ; 64/60 ; 96 ; 96/31 ; 96/95 ; Aging ; Amplification ; Animals ; Cell cycle ; Cell Dedifferentiation ; Cell Lineage ; Cell self-renewal ; Cellular Microenvironment ; Gene sequencing ; Hair ; Hair Color - physiology ; Hair Follicle - cytology ; Homeostasis ; Humanities and Social Sciences ; Humans ; Hypotheses ; Melanocytes - cytology ; Mice ; Morphology ; multidisciplinary ; Progeny ; Science ; Science (multidisciplinary) ; Stem Cell Niche ; Stem cells ; Stem Cells - cytology ; Transit ; Volumetric analysis ; Wnt protein</subject><ispartof>Nature (London), 2023-04, Vol.616 (7958), p.774-782</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>Copyright Nature Publishing Group Apr 27, 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-7077cb183b25496275f586c87e1c1afabb604ae8eeaeb4c2a6e90acb5394be2d3</citedby><cites>FETCH-LOGICAL-c475t-7077cb183b25496275f586c87e1c1afabb604ae8eeaeb4c2a6e90acb5394be2d3</cites><orcidid>0000-0002-5597-5994 ; 0000-0002-9032-4505 ; 0000-0001-7340-8427 ; 0000-0002-4519-1950 ; 0000-0003-4930-1739 ; 0000-0001-8792-6890 ; 0000-0003-1124-4572 ; 0000-0002-0495-1407 ; 0000-0002-0787-6748</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37076619$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sun, Qi</creatorcontrib><creatorcontrib>Lee, Wendy</creatorcontrib><creatorcontrib>Hu, Hai</creatorcontrib><creatorcontrib>Ogawa, Tatsuya</creatorcontrib><creatorcontrib>De Leon, Sophie</creatorcontrib><creatorcontrib>Katehis, Ioanna</creatorcontrib><creatorcontrib>Lim, Chae Ho</creatorcontrib><creatorcontrib>Takeo, Makoto</creatorcontrib><creatorcontrib>Cammer, Michael</creatorcontrib><creatorcontrib>Taketo, M. Mark</creatorcontrib><creatorcontrib>Gay, Denise L.</creatorcontrib><creatorcontrib>Millar, Sarah E.</creatorcontrib><creatorcontrib>Ito, Mayumi</creatorcontrib><title>Dedifferentiation maintains melanocyte stem cells in a dynamic niche</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>For unknow reasons, the melanocyte stem cell (McSC) system fails earlier than other adult stem cell populations
1
, which leads to hair greying in most humans and mice
2
,
3
. Current dogma states that McSCs are reserved in an undifferentiated state in the hair follicle niche, physically segregated from differentiated progeny that migrate away following cues of regenerative stimuli
4
–
8
. Here we show that most McSCs toggle between transit-amplifying and stem cell states for both self-renewal and generation of mature progeny, a mechanism fundamentally distinct from those of other self-renewing systems. Live imaging and single-cell RNA sequencing revealed that McSCs are mobile, translocating between hair follicle stem cell and transit-amplifying compartments where they reversibly enter distinct differentiation states governed by local microenvironmental cues (for example, WNT). Long-term lineage tracing demonstrated that the McSC system is maintained by reverted McSCs rather than by reserved stem cells inherently exempt from reversible changes. During ageing, there is accumulation of stranded McSCs that do not contribute to the regeneration of melanocyte progeny. These results identify a new model whereby dedifferentiation is integral to homeostatic stem cell maintenance and suggest that modulating McSC mobility may represent a new approach for the prevention of hair greying.
Local microenvironmental cues modulate melanocyte stem cells, which control hair pigmentation, to enter different differentiation states, shifting between hair follicle stem cell and transit-amplifying compartments, a process that is different to other self-renewing systems.</description><subject>13/100</subject><subject>13/51</subject><subject>14</subject><subject>14/1</subject><subject>14/19</subject><subject>14/32</subject><subject>14/63</subject><subject>14/69</subject><subject>45/91</subject><subject>631/532/2118/2438</subject><subject>631/532/7</subject><subject>64</subject><subject>64/60</subject><subject>96</subject><subject>96/31</subject><subject>96/95</subject><subject>Aging</subject><subject>Amplification</subject><subject>Animals</subject><subject>Cell cycle</subject><subject>Cell Dedifferentiation</subject><subject>Cell Lineage</subject><subject>Cell self-renewal</subject><subject>Cellular Microenvironment</subject><subject>Gene sequencing</subject><subject>Hair</subject><subject>Hair Color - physiology</subject><subject>Hair Follicle - cytology</subject><subject>Homeostasis</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Melanocytes - cytology</subject><subject>Mice</subject><subject>Morphology</subject><subject>multidisciplinary</subject><subject>Progeny</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Stem Cell Niche</subject><subject>Stem cells</subject><subject>Stem Cells - cytology</subject><subject>Transit</subject><subject>Volumetric analysis</subject><subject>Wnt protein</subject><issn>0028-0836</issn><issn>1476-4687</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kUtv2zAQhImiQe24_QM9BAJ66UXJ8iGSOgWF8ypgoJfkTFD0KqEhUQkpB_C_L1WnTtJDDwQP--3sDIaQrxROKXB9lgSttCyB8RKqWkIpP5A5FUqWQmr1kcwBmC5BczkjxyltAKCiSnwiM65ASUnrObm4wLVvW4wYRm9HP4Sitz6M-aWix86Gwe1GLNKIfeGw61LhQ2GL9S7Y3rsiePeAn8lRa7uEX17-Bbm7urxd3pSrX9c_lz9WpROqGst8VLmGat6wStSSqarN_p1WSB21rW0aCcKiRrTYCMesxBqsaypeiwbZmi_I-V73cdv0uHbZc7SdeYy-t3FnBuvN-0nwD-Z-eDYUKGe1rrPC9xeFODxtMY2m92mKZQMO22SYBl5LrrPJBfn2D7oZtjHkfBOlBBVSTYJsT7k4pBSxPbihYKaWzL4lk1syf1oyMi-dvM1xWPlbSwb4Hkh5FO4xvt7-j-xvlVWedA</recordid><startdate>20230427</startdate><enddate>20230427</enddate><creator>Sun, Qi</creator><creator>Lee, Wendy</creator><creator>Hu, Hai</creator><creator>Ogawa, Tatsuya</creator><creator>De Leon, Sophie</creator><creator>Katehis, Ioanna</creator><creator>Lim, Chae Ho</creator><creator>Takeo, Makoto</creator><creator>Cammer, Michael</creator><creator>Taketo, M. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sun, Qi</au><au>Lee, Wendy</au><au>Hu, Hai</au><au>Ogawa, Tatsuya</au><au>De Leon, Sophie</au><au>Katehis, Ioanna</au><au>Lim, Chae Ho</au><au>Takeo, Makoto</au><au>Cammer, Michael</au><au>Taketo, M. Mark</au><au>Gay, Denise L.</au><au>Millar, Sarah E.</au><au>Ito, Mayumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dedifferentiation maintains melanocyte stem cells in a dynamic niche</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2023-04-27</date><risdate>2023</risdate><volume>616</volume><issue>7958</issue><spage>774</spage><epage>782</epage><pages>774-782</pages><issn>0028-0836</issn><issn>1476-4687</issn><eissn>1476-4687</eissn><abstract>For unknow reasons, the melanocyte stem cell (McSC) system fails earlier than other adult stem cell populations
1
, which leads to hair greying in most humans and mice
2
,
3
. Current dogma states that McSCs are reserved in an undifferentiated state in the hair follicle niche, physically segregated from differentiated progeny that migrate away following cues of regenerative stimuli
4
–
8
. Here we show that most McSCs toggle between transit-amplifying and stem cell states for both self-renewal and generation of mature progeny, a mechanism fundamentally distinct from those of other self-renewing systems. Live imaging and single-cell RNA sequencing revealed that McSCs are mobile, translocating between hair follicle stem cell and transit-amplifying compartments where they reversibly enter distinct differentiation states governed by local microenvironmental cues (for example, WNT). Long-term lineage tracing demonstrated that the McSC system is maintained by reverted McSCs rather than by reserved stem cells inherently exempt from reversible changes. During ageing, there is accumulation of stranded McSCs that do not contribute to the regeneration of melanocyte progeny. These results identify a new model whereby dedifferentiation is integral to homeostatic stem cell maintenance and suggest that modulating McSC mobility may represent a new approach for the prevention of hair greying.
Local microenvironmental cues modulate melanocyte stem cells, which control hair pigmentation, to enter different differentiation states, shifting between hair follicle stem cell and transit-amplifying compartments, a process that is different to other self-renewing systems.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37076619</pmid><doi>10.1038/s41586-023-05960-6</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5597-5994</orcidid><orcidid>https://orcid.org/0000-0002-9032-4505</orcidid><orcidid>https://orcid.org/0000-0001-7340-8427</orcidid><orcidid>https://orcid.org/0000-0002-4519-1950</orcidid><orcidid>https://orcid.org/0000-0003-4930-1739</orcidid><orcidid>https://orcid.org/0000-0001-8792-6890</orcidid><orcidid>https://orcid.org/0000-0003-1124-4572</orcidid><orcidid>https://orcid.org/0000-0002-0495-1407</orcidid><orcidid>https://orcid.org/0000-0002-0787-6748</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10132989 |
source | Nature Journals Online |
subjects | 13/100 13/51 14 14/1 14/19 14/32 14/63 14/69 45/91 631/532/2118/2438 631/532/7 64 64/60 96 96/31 96/95 Aging Amplification Animals Cell cycle Cell Dedifferentiation Cell Lineage Cell self-renewal Cellular Microenvironment Gene sequencing Hair Hair Color - physiology Hair Follicle - cytology Homeostasis Humanities and Social Sciences Humans Hypotheses Melanocytes - cytology Mice Morphology multidisciplinary Progeny Science Science (multidisciplinary) Stem Cell Niche Stem cells Stem Cells - cytology Transit Volumetric analysis Wnt protein |
title | Dedifferentiation maintains melanocyte stem cells in a dynamic niche |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T09%3A24%3A56IST&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=Dedifferentiation%20maintains%20melanocyte%20stem%20cells%20in%20a%20dynamic%20niche&rft.jtitle=Nature%20(London)&rft.au=Sun,%20Qi&rft.date=2023-04-27&rft.volume=616&rft.issue=7958&rft.spage=774&rft.epage=782&rft.pages=774-782&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/s41586-023-05960-6&rft_dat=%3Cproquest_pubme%3E2807414679%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c475t-7077cb183b25496275f586c87e1c1afabb604ae8eeaeb4c2a6e90acb5394be2d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2807414679&rft_id=info:pmid/37076619&rfr_iscdi=true |