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A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle
A progenitor cell could generate a certain type or multiple types of descendant cells during embryonic development. To make all the descendant cell types and developmental trajectories of every single progenitor cell clear remains an ultimate goal in developmental biology. Characterizations of desce...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2021-06, Vol.118 (25), p.1-9 |
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creator | Yang, Yun Wang, Hao He, Jia Shi, Wenchao Jiang, Zhanmei Gao, Lina Jiang, Yan Ni, Rui Yang, Qifen Luo, Lingfei |
description | A progenitor cell could generate a certain type or multiple types of descendant cells during embryonic development. To make all the descendant cell types and developmental trajectories of every single progenitor cell clear remains an ultimate goal in developmental biology. Characterizations of descendant cells produced by each uncommitted progenitor for a full germ layer represent a big step toward the goal. Here, we focus on early foregut endoderm, which generates foregut digestive organs, including the pancreas, liver, foregut, and ductal system, through distinct lineages. Using unbiased single-cell labeling techniques, we label every individual zebrafish foregut endodermal progenitor cell out of 216 cells to visibly trace the distribution and number of their descendant cells. Hence, single-cell–resolution fate and proliferation maps of early foregut endoderm are established, in which progenitor regions of each foregut digestive organ are precisely demarcated. The maps indicate that the pancreatic endocrine progenitors are featured by a cell cycle state with a long G1 phase. Manipulating durations of the G1 phase modulates pancreatic progenitor populations. This study illustrates foregut endodermal progenitor cell fate at singlecell resolution, precisely demarcates different progenitor populations, and sheds light on mechanistic insights into pancreatic fate determination. |
doi_str_mv | 10.1073/pnas.2025793118 |
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To make all the descendant cell types and developmental trajectories of every single progenitor cell clear remains an ultimate goal in developmental biology. Characterizations of descendant cells produced by each uncommitted progenitor for a full germ layer represent a big step toward the goal. Here, we focus on early foregut endoderm, which generates foregut digestive organs, including the pancreas, liver, foregut, and ductal system, through distinct lineages. Using unbiased single-cell labeling techniques, we label every individual zebrafish foregut endodermal progenitor cell out of 216 cells to visibly trace the distribution and number of their descendant cells. Hence, single-cell–resolution fate and proliferation maps of early foregut endoderm are established, in which progenitor regions of each foregut digestive organ are precisely demarcated. The maps indicate that the pancreatic endocrine progenitors are featured by a cell cycle state with a long G1 phase. Manipulating durations of the G1 phase modulates pancreatic progenitor populations. This study illustrates foregut endodermal progenitor cell fate at singlecell resolution, precisely demarcates different progenitor populations, and sheds light on mechanistic insights into pancreatic fate determination.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2025793118</identifier><identifier>PMID: 34161274</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Biological Sciences ; Cell Cycle ; Cell fate ; Cell Lineage ; Cell Proliferation ; Cells (biology) ; Developmental biology ; Embryogenesis ; Embryonic growth stage ; Endoderm ; Endoderm - cytology ; Foregut ; G1 Phase ; Hedgehog Proteins - metabolism ; Pancreas ; Pancreas - cytology ; Population studies ; Populations ; Progenitor cells ; Signal Transduction ; Single-Cell Analysis ; Stem cells ; Stem Cells - cytology ; Zebrafish ; Zebrafish - embryology ; Zebrafish Proteins - metabolism</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (25), p.1-9</ispartof><rights>Copyright National Academy of Sciences Jun 22, 2021</rights><rights>2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-b8d0babdc379e6755896143a84098a4b22c68bcb21a553f62a4589ac5abd4b003</citedby><cites>FETCH-LOGICAL-c443t-b8d0babdc379e6755896143a84098a4b22c68bcb21a553f62a4589ac5abd4b003</cites><orcidid>0000-0001-9341-8518 ; 0000-0002-4525-9513 ; 0000-0002-9035-7526 ; 0000-0001-7273-102X ; 0000-0003-0689-5477 ; 0000-0002-8621-993X ; 0000-0002-9868-7589 ; 0000-0001-6135-816X ; 0000-0001-8009-5246</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/27041082$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/27041082$$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/34161274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Yun</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><creatorcontrib>He, Jia</creatorcontrib><creatorcontrib>Shi, Wenchao</creatorcontrib><creatorcontrib>Jiang, Zhanmei</creatorcontrib><creatorcontrib>Gao, Lina</creatorcontrib><creatorcontrib>Jiang, Yan</creatorcontrib><creatorcontrib>Ni, Rui</creatorcontrib><creatorcontrib>Yang, Qifen</creatorcontrib><creatorcontrib>Luo, Lingfei</creatorcontrib><title>A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>A progenitor cell could generate a certain type or multiple types of descendant cells during embryonic development. To make all the descendant cell types and developmental trajectories of every single progenitor cell clear remains an ultimate goal in developmental biology. Characterizations of descendant cells produced by each uncommitted progenitor for a full germ layer represent a big step toward the goal. Here, we focus on early foregut endoderm, which generates foregut digestive organs, including the pancreas, liver, foregut, and ductal system, through distinct lineages. Using unbiased single-cell labeling techniques, we label every individual zebrafish foregut endodermal progenitor cell out of 216 cells to visibly trace the distribution and number of their descendant cells. Hence, single-cell–resolution fate and proliferation maps of early foregut endoderm are established, in which progenitor regions of each foregut digestive organ are precisely demarcated. The maps indicate that the pancreatic endocrine progenitors are featured by a cell cycle state with a long G1 phase. Manipulating durations of the G1 phase modulates pancreatic progenitor populations. This study illustrates foregut endodermal progenitor cell fate at singlecell resolution, precisely demarcates different progenitor populations, and sheds light on mechanistic insights into pancreatic fate determination.</description><subject>Animals</subject><subject>Biological Sciences</subject><subject>Cell Cycle</subject><subject>Cell fate</subject><subject>Cell Lineage</subject><subject>Cell Proliferation</subject><subject>Cells (biology)</subject><subject>Developmental biology</subject><subject>Embryogenesis</subject><subject>Embryonic growth stage</subject><subject>Endoderm</subject><subject>Endoderm - cytology</subject><subject>Foregut</subject><subject>G1 Phase</subject><subject>Hedgehog Proteins - metabolism</subject><subject>Pancreas</subject><subject>Pancreas - cytology</subject><subject>Population studies</subject><subject>Populations</subject><subject>Progenitor cells</subject><subject>Signal Transduction</subject><subject>Single-Cell Analysis</subject><subject>Stem cells</subject><subject>Stem Cells - cytology</subject><subject>Zebrafish</subject><subject>Zebrafish - embryology</subject><subject>Zebrafish Proteins - metabolism</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkUtv1DAUhS1ERYfCmhXIEhs2aa8fiZ0NUlWVh1SpG1hbjnMzZEjsYCeVZsd_6D_kl-AwZXisLOt-5-ieewh5weCcgRIXk7fpnAMvVS0Y04_IhkHNikrW8JhsALgqtOTylDxNaQcAdanhCTkVklWMK7khXy9p6v12wMLhMPz4fh8xhWGZ--BpZ2eko51o6Cj6NrQYRxrxDu2QaIujjc7-AvN8st5FzF9Hpxi26Ps5xESbPV19qdu7AZ-Rky5L8fnDe0Y-v7v-dPWhuLl9__Hq8qZwUoq5aHQLjW1aJ1SNlSpLXVdMCqsl1NrKhnNX6cY1nNmyFF3FrcyIdWXWyAZAnJG3B99paUZsHfo52sFMsc8r702wvfl34vsvZhvujOZCVYpngzcPBjF8WzDNZuzTmsN6DEsyvJRSK62lzujr_9BdWKLP8VaqYqICUWbq4kC5GFKK2B2XYWDWIs1apPlTZFa8-jvDkf_dXAZeHoBdypc-zrkCySAH-QnBPKYp</recordid><startdate>20210622</startdate><enddate>20210622</enddate><creator>Yang, Yun</creator><creator>Wang, Hao</creator><creator>He, Jia</creator><creator>Shi, Wenchao</creator><creator>Jiang, Zhanmei</creator><creator>Gao, Lina</creator><creator>Jiang, Yan</creator><creator>Ni, Rui</creator><creator>Yang, Qifen</creator><creator>Luo, Lingfei</creator><general>National Academy of Sciences</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><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>5PM</scope><orcidid>https://orcid.org/0000-0001-9341-8518</orcidid><orcidid>https://orcid.org/0000-0002-4525-9513</orcidid><orcidid>https://orcid.org/0000-0002-9035-7526</orcidid><orcidid>https://orcid.org/0000-0001-7273-102X</orcidid><orcidid>https://orcid.org/0000-0003-0689-5477</orcidid><orcidid>https://orcid.org/0000-0002-8621-993X</orcidid><orcidid>https://orcid.org/0000-0002-9868-7589</orcidid><orcidid>https://orcid.org/0000-0001-6135-816X</orcidid><orcidid>https://orcid.org/0000-0001-8009-5246</orcidid></search><sort><creationdate>20210622</creationdate><title>A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle</title><author>Yang, Yun ; 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To make all the descendant cell types and developmental trajectories of every single progenitor cell clear remains an ultimate goal in developmental biology. Characterizations of descendant cells produced by each uncommitted progenitor for a full germ layer represent a big step toward the goal. Here, we focus on early foregut endoderm, which generates foregut digestive organs, including the pancreas, liver, foregut, and ductal system, through distinct lineages. Using unbiased single-cell labeling techniques, we label every individual zebrafish foregut endodermal progenitor cell out of 216 cells to visibly trace the distribution and number of their descendant cells. Hence, single-cell–resolution fate and proliferation maps of early foregut endoderm are established, in which progenitor regions of each foregut digestive organ are precisely demarcated. The maps indicate that the pancreatic endocrine progenitors are featured by a cell cycle state with a long G1 phase. 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subjects | Animals Biological Sciences Cell Cycle Cell fate Cell Lineage Cell Proliferation Cells (biology) Developmental biology Embryogenesis Embryonic growth stage Endoderm Endoderm - cytology Foregut G1 Phase Hedgehog Proteins - metabolism Pancreas Pancreas - cytology Population studies Populations Progenitor cells Signal Transduction Single-Cell Analysis Stem cells Stem Cells - cytology Zebrafish Zebrafish - embryology Zebrafish Proteins - metabolism |
title | A single-cell–resolution fate map of endoderm reveals demarcation of pancreatic progenitors by cell cycle |
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