Headcase promotes cell survival and niche maintenance in the Drosophila testis
At the apical tip of the Drosophila testis, germline and somatic stem cells surround a cluster of somatic cells called the hub. Hub cells produce a self-renewal factor, Unpaired (Upd), that activates the JAK-STAT pathway in adjacent stem cells to regulate stem cell behavior. Therefore, apical hub ce...
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description | At the apical tip of the Drosophila testis, germline and somatic stem cells surround a cluster of somatic cells called the hub. Hub cells produce a self-renewal factor, Unpaired (Upd), that activates the JAK-STAT pathway in adjacent stem cells to regulate stem cell behavior. Therefore, apical hub cells are a critical component of the stem cell niche in the testis. In the course of a screen to identify factors involved in regulating hub maintenance, we identified headcase (hdc). Hub cells depleted for hdc undergo programmed cell death, suggesting that anti-apoptotic pathways play an important role in maintenance of the niche. Using hdc as paradigm, we describe here the first comprehensive analysis on the effects of a progressive niche reduction on the testis stem cell pool. Surprisingly, single hub cells remain capable of supporting numerous stem cells, indicating that although the size and number of niche support cells influence stem cell maintenance, the testis stem cell niche appears to be remarkably robust in the its ability to support stem cells after severe damage. |
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Hub cells produce a self-renewal factor, Unpaired (Upd), that activates the JAK-STAT pathway in adjacent stem cells to regulate stem cell behavior. Therefore, apical hub cells are a critical component of the stem cell niche in the testis. In the course of a screen to identify factors involved in regulating hub maintenance, we identified headcase (hdc). Hub cells depleted for hdc undergo programmed cell death, suggesting that anti-apoptotic pathways play an important role in maintenance of the niche. Using hdc as paradigm, we describe here the first comprehensive analysis on the effects of a progressive niche reduction on the testis stem cell pool. Surprisingly, single hub cells remain capable of supporting numerous stem cells, indicating that although the size and number of niche support cells influence stem cell maintenance, the testis stem cell niche appears to be remarkably robust in the its ability to support stem cells after severe damage.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0068026</identifier><identifier>PMID: 23874487</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Animals ; Apoptosis ; Apoptosis - genetics ; Biology ; Cell death ; Cell self-renewal ; Cell survival ; Cell Survival - genetics ; Cysts ; Drosophila ; Drosophila - genetics ; Drosophila - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Gene expression ; Genetics ; Homeostasis ; Insects ; Kinases ; Laboratories ; Maintenance ; Male ; Photoreceptors ; RNA Interference ; Somatic cells ; Sperm ; Stem Cell Niche - physiology ; Stem cells ; Stem Cells - metabolism ; Testis - metabolism ; Transcriptome ; Underpotential deposition</subject><ispartof>PloS one, 2013-07, Vol.8 (7), p.e68026-e68026</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Resende et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Resende et al 2013 Resende et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-38d15ed1e4ecdf29aeb1c20c70c4893ccb3de5fb6f4e5bab8a55b33e12a10a823</citedby><cites>FETCH-LOGICAL-c692t-38d15ed1e4ecdf29aeb1c20c70c4893ccb3de5fb6f4e5bab8a55b33e12a10a823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706621/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706621/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23874487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bökel, Christian</contributor><creatorcontrib>Resende, Luís Pedro F</creatorcontrib><creatorcontrib>Boyle, Monica</creatorcontrib><creatorcontrib>Tran, Darrell</creatorcontrib><creatorcontrib>Fellner, Thomas</creatorcontrib><creatorcontrib>Jones, D Leanne</creatorcontrib><title>Headcase promotes cell survival and niche maintenance in the Drosophila testis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>At the apical tip of the Drosophila testis, germline and somatic stem cells surround a cluster of somatic cells called the hub. Hub cells produce a self-renewal factor, Unpaired (Upd), that activates the JAK-STAT pathway in adjacent stem cells to regulate stem cell behavior. Therefore, apical hub cells are a critical component of the stem cell niche in the testis. In the course of a screen to identify factors involved in regulating hub maintenance, we identified headcase (hdc). Hub cells depleted for hdc undergo programmed cell death, suggesting that anti-apoptotic pathways play an important role in maintenance of the niche. Using hdc as paradigm, we describe here the first comprehensive analysis on the effects of a progressive niche reduction on the testis stem cell pool. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Resende, Luís Pedro F</au><au>Boyle, Monica</au><au>Tran, Darrell</au><au>Fellner, Thomas</au><au>Jones, D Leanne</au><au>Bökel, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Headcase promotes cell survival and niche maintenance in the Drosophila testis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-07-09</date><risdate>2013</risdate><volume>8</volume><issue>7</issue><spage>e68026</spage><epage>e68026</epage><pages>e68026-e68026</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>At the apical tip of the Drosophila testis, germline and somatic stem cells surround a cluster of somatic cells called the hub. Hub cells produce a self-renewal factor, Unpaired (Upd), that activates the JAK-STAT pathway in adjacent stem cells to regulate stem cell behavior. Therefore, apical hub cells are a critical component of the stem cell niche in the testis. In the course of a screen to identify factors involved in regulating hub maintenance, we identified headcase (hdc). Hub cells depleted for hdc undergo programmed cell death, suggesting that anti-apoptotic pathways play an important role in maintenance of the niche. Using hdc as paradigm, we describe here the first comprehensive analysis on the effects of a progressive niche reduction on the testis stem cell pool. Surprisingly, single hub cells remain capable of supporting numerous stem cells, indicating that although the size and number of niche support cells influence stem cell maintenance, the testis stem cell niche appears to be remarkably robust in the its ability to support stem cells after severe damage.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23874487</pmid><doi>10.1371/journal.pone.0068026</doi><tpages>e68026</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Apoptosis Apoptosis - genetics Biology Cell death Cell self-renewal Cell survival Cell Survival - genetics Cysts Drosophila Drosophila - genetics Drosophila - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Gene expression Genetics Homeostasis Insects Kinases Laboratories Maintenance Male Photoreceptors RNA Interference Somatic cells Sperm Stem Cell Niche - physiology Stem cells Stem Cells - metabolism Testis - metabolism Transcriptome Underpotential deposition |
title | Headcase promotes cell survival and niche maintenance in the Drosophila testis |
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