Identification of multipotent mammary stem cells by protein C receptor expression
Using transplantation and lineage-tracing strategies, protein C receptor is identified as a marker of mammary stem cells in mice, with potential implications for understanding the initiation of breast cancer. Procr link to mammary stem cell multipotency Using transplantation and lineage tracing stra...
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Veröffentlicht in: | Nature (London) 2015-01, Vol.517 (7532), p.81-84 |
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description | Using transplantation and lineage-tracing strategies, protein C receptor is identified as a marker of mammary stem cells in mice, with potential implications for understanding the initiation of breast cancer.
Procr link to mammary stem cell multipotency
Using transplantation and lineage tracing strategies, Yi Zeng and colleagues have identified protein C receptor (Procr), a target for Wnt signalling proteins in the mammary gland, as a marker of mammary stem cells. Procr is exclusively expressed in a small subset of the basal/stem cell-enriched but not the luminal cell population of mouse mammary glands. The authors suggest that the identification of this new population of multipotent mammary stem cells could be important in the understanding of initiation of breast cancer.
The mammary gland is composed of multiple types of epithelial cells, which are generated by mammary stem cells (MaSCs) residing at the top of the hierarchy
1
,
2
. However, the existence of these multipotent MaSCs remains controversial and the nature of such cells is unknown
3
,
4
. Here we demonstrate that protein C receptor (Procr), a novel Wnt target in the mammary gland, marks a unique population of multipotent mouse MaSCs. Procr-positive cells localize to the basal layer, exhibit epithelial-to-mesenchymal transition characteristics, and express low levels of basal keratins. Procr-expressing cells have a high regenerative capacity in transplantation assays and differentiate into all lineages of the mammary epithelium by lineage tracing. These results define a novel multipotent mammary stem cell population that could be important in the initiation of breast cancer. |
doi_str_mv | 10.1038/nature13851 |
format | Article |
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Procr link to mammary stem cell multipotency
Using transplantation and lineage tracing strategies, Yi Zeng and colleagues have identified protein C receptor (Procr), a target for Wnt signalling proteins in the mammary gland, as a marker of mammary stem cells. Procr is exclusively expressed in a small subset of the basal/stem cell-enriched but not the luminal cell population of mouse mammary glands. The authors suggest that the identification of this new population of multipotent mammary stem cells could be important in the understanding of initiation of breast cancer.
The mammary gland is composed of multiple types of epithelial cells, which are generated by mammary stem cells (MaSCs) residing at the top of the hierarchy
1
,
2
. However, the existence of these multipotent MaSCs remains controversial and the nature of such cells is unknown
3
,
4
. Here we demonstrate that protein C receptor (Procr), a novel Wnt target in the mammary gland, marks a unique population of multipotent mouse MaSCs. Procr-positive cells localize to the basal layer, exhibit epithelial-to-mesenchymal transition characteristics, and express low levels of basal keratins. Procr-expressing cells have a high regenerative capacity in transplantation assays and differentiate into all lineages of the mammary epithelium by lineage tracing. These results define a novel multipotent mammary stem cell population that could be important in the initiation of breast cancer.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature13851</identifier><identifier>PMID: 25327250</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/100 ; 13/31 ; 13/95 ; 14/19 ; 38/23 ; 38/61 ; 631/136/532/2436 ; 631/532/2436 ; 64/60 ; Animals ; Biomarkers - metabolism ; Cell Lineage ; Cell Tracking ; Endothelial Protein C Receptor ; Female ; Gene Knock-In Techniques ; Humanities and Social Sciences ; Keratins - metabolism ; letter ; Male ; Mammary glands ; Mammary Glands, Animal - cytology ; Mammary Glands, Animal - metabolism ; Mice ; multidisciplinary ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - metabolism ; Physiological aspects ; Protein C ; Receptors, Cell Surface - metabolism ; Regeneration ; Science ; Stem cells ; Structure</subject><ispartof>Nature (London), 2015-01, Vol.517 (7532), p.81-84</ispartof><rights>Springer Nature Limited 2014</rights><rights>COPYRIGHT 2015 Nature Publishing Group</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3701-44e71cc89dd7b9518eacdbd5285ff8e6b79eb1909329e13e025a54ee94ddbed03</citedby><cites>FETCH-LOGICAL-c3701-44e71cc89dd7b9518eacdbd5285ff8e6b79eb1909329e13e025a54ee94ddbed03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature13851$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature13851$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25327250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Daisong</creatorcontrib><creatorcontrib>Cai, Cheguo</creatorcontrib><creatorcontrib>Dong, Xiaobing</creatorcontrib><creatorcontrib>Yu, Qing Cissy</creatorcontrib><creatorcontrib>Zhang, Xiao-Ou</creatorcontrib><creatorcontrib>Yang, Li</creatorcontrib><creatorcontrib>Zeng, Yi Arial</creatorcontrib><title>Identification of multipotent mammary stem cells by protein C receptor expression</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Using transplantation and lineage-tracing strategies, protein C receptor is identified as a marker of mammary stem cells in mice, with potential implications for understanding the initiation of breast cancer.
Procr link to mammary stem cell multipotency
Using transplantation and lineage tracing strategies, Yi Zeng and colleagues have identified protein C receptor (Procr), a target for Wnt signalling proteins in the mammary gland, as a marker of mammary stem cells. Procr is exclusively expressed in a small subset of the basal/stem cell-enriched but not the luminal cell population of mouse mammary glands. The authors suggest that the identification of this new population of multipotent mammary stem cells could be important in the understanding of initiation of breast cancer.
The mammary gland is composed of multiple types of epithelial cells, which are generated by mammary stem cells (MaSCs) residing at the top of the hierarchy
1
,
2
. However, the existence of these multipotent MaSCs remains controversial and the nature of such cells is unknown
3
,
4
. Here we demonstrate that protein C receptor (Procr), a novel Wnt target in the mammary gland, marks a unique population of multipotent mouse MaSCs. Procr-positive cells localize to the basal layer, exhibit epithelial-to-mesenchymal transition characteristics, and express low levels of basal keratins. Procr-expressing cells have a high regenerative capacity in transplantation assays and differentiate into all lineages of the mammary epithelium by lineage tracing. These results define a novel multipotent mammary stem cell population that could be important in the initiation of breast cancer.</description><subject>13/100</subject><subject>13/31</subject><subject>13/95</subject><subject>14/19</subject><subject>38/23</subject><subject>38/61</subject><subject>631/136/532/2436</subject><subject>631/532/2436</subject><subject>64/60</subject><subject>Animals</subject><subject>Biomarkers - metabolism</subject><subject>Cell Lineage</subject><subject>Cell Tracking</subject><subject>Endothelial Protein C Receptor</subject><subject>Female</subject><subject>Gene Knock-In Techniques</subject><subject>Humanities and Social Sciences</subject><subject>Keratins - metabolism</subject><subject>letter</subject><subject>Male</subject><subject>Mammary glands</subject><subject>Mammary Glands, Animal - cytology</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Mice</subject><subject>multidisciplinary</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - metabolism</subject><subject>Physiological aspects</subject><subject>Protein C</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Regeneration</subject><subject>Science</subject><subject>Stem cells</subject><subject>Structure</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0c1r2zAYBnAxNpq03Wn3IbZTWZ1KtmVLxxLaNVAY_dhZyNLroGDLniRD-99PJVtJwOggeN-fHhAPQl8oWVFS8Cun4uSBFpzRD2hJy7rKyorXH9GSkJxnhBfVAp2GsCOEMFqXJ2iRsyKvc0aW6GFjwEXbWq2iHRweWtxPXbTjENMc96rvlX_FIUKPNXRdwM0rHn3aWofX2IOGMQ4ew8voIYQUcY4-taoL8PnffYZ-3948r--y-18_N-vr-0wXNaFZWUJNtebCmLoRjHJQ2jSG5Zy1LYeqqQU0VBBR5CJ9DkjOFCsBRGlMA4YUZ-j7PnerOpDWtUP0Svc2aHldiKrMRVXRpLIZtQUHXnWDg9am8ZH_NuP1aP_IQ7SaQekY6K2eTb04epBMhJe4VVMIcvP0eGx_7K32QwgeWjl6-1aCpES-FS4PCk_6616PU9ODebf_G07gcg9CWrkteLkbJu9SM7N5fwF8yLRQ</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Wang, Daisong</creator><creator>Cai, Cheguo</creator><creator>Dong, Xiaobing</creator><creator>Yu, Qing Cissy</creator><creator>Zhang, Xiao-Ou</creator><creator>Yang, Li</creator><creator>Zeng, Yi Arial</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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></search><sort><creationdate>20150101</creationdate><title>Identification of multipotent mammary stem cells by protein C receptor expression</title><author>Wang, Daisong ; Cai, Cheguo ; Dong, Xiaobing ; Yu, Qing Cissy ; Zhang, Xiao-Ou ; Yang, Li ; Zeng, Yi Arial</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3701-44e71cc89dd7b9518eacdbd5285ff8e6b79eb1909329e13e025a54ee94ddbed03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>13/100</topic><topic>13/31</topic><topic>13/95</topic><topic>14/19</topic><topic>38/23</topic><topic>38/61</topic><topic>631/136/532/2436</topic><topic>631/532/2436</topic><topic>64/60</topic><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>Cell Lineage</topic><topic>Cell Tracking</topic><topic>Endothelial Protein C Receptor</topic><topic>Female</topic><topic>Gene Knock-In Techniques</topic><topic>Humanities and Social Sciences</topic><topic>Keratins - metabolism</topic><topic>letter</topic><topic>Male</topic><topic>Mammary glands</topic><topic>Mammary Glands, Animal - cytology</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Mice</topic><topic>multidisciplinary</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - metabolism</topic><topic>Physiological aspects</topic><topic>Protein C</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Regeneration</topic><topic>Science</topic><topic>Stem cells</topic><topic>Structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Daisong</creatorcontrib><creatorcontrib>Cai, Cheguo</creatorcontrib><creatorcontrib>Dong, Xiaobing</creatorcontrib><creatorcontrib>Yu, Qing Cissy</creatorcontrib><creatorcontrib>Zhang, Xiao-Ou</creatorcontrib><creatorcontrib>Yang, Li</creatorcontrib><creatorcontrib>Zeng, Yi Arial</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Daisong</au><au>Cai, Cheguo</au><au>Dong, Xiaobing</au><au>Yu, Qing Cissy</au><au>Zhang, Xiao-Ou</au><au>Yang, Li</au><au>Zeng, Yi Arial</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of multipotent mammary stem cells by protein C receptor expression</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>517</volume><issue>7532</issue><spage>81</spage><epage>84</epage><pages>81-84</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>Using transplantation and lineage-tracing strategies, protein C receptor is identified as a marker of mammary stem cells in mice, with potential implications for understanding the initiation of breast cancer.
Procr link to mammary stem cell multipotency
Using transplantation and lineage tracing strategies, Yi Zeng and colleagues have identified protein C receptor (Procr), a target for Wnt signalling proteins in the mammary gland, as a marker of mammary stem cells. Procr is exclusively expressed in a small subset of the basal/stem cell-enriched but not the luminal cell population of mouse mammary glands. The authors suggest that the identification of this new population of multipotent mammary stem cells could be important in the understanding of initiation of breast cancer.
The mammary gland is composed of multiple types of epithelial cells, which are generated by mammary stem cells (MaSCs) residing at the top of the hierarchy
1
,
2
. However, the existence of these multipotent MaSCs remains controversial and the nature of such cells is unknown
3
,
4
. Here we demonstrate that protein C receptor (Procr), a novel Wnt target in the mammary gland, marks a unique population of multipotent mouse MaSCs. Procr-positive cells localize to the basal layer, exhibit epithelial-to-mesenchymal transition characteristics, and express low levels of basal keratins. Procr-expressing cells have a high regenerative capacity in transplantation assays and differentiate into all lineages of the mammary epithelium by lineage tracing. These results define a novel multipotent mammary stem cell population that could be important in the initiation of breast cancer.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>25327250</pmid><doi>10.1038/nature13851</doi><tpages>4</tpages></addata></record> |
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subjects | 13/100 13/31 13/95 14/19 38/23 38/61 631/136/532/2436 631/532/2436 64/60 Animals Biomarkers - metabolism Cell Lineage Cell Tracking Endothelial Protein C Receptor Female Gene Knock-In Techniques Humanities and Social Sciences Keratins - metabolism letter Male Mammary glands Mammary Glands, Animal - cytology Mammary Glands, Animal - metabolism Mice multidisciplinary Multipotent Stem Cells - cytology Multipotent Stem Cells - metabolism Physiological aspects Protein C Receptors, Cell Surface - metabolism Regeneration Science Stem cells Structure |
title | Identification of multipotent mammary stem cells by protein C receptor expression |
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