Exploring the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation
We explored the underlying mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation (cell type switchings) from landscape and flux perspectives. Lineage reprogramming is a new regenerative method to convert a matured cell into another cell including direct transdiffer...
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description | We explored the underlying mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation (cell type switchings) from landscape and flux perspectives. Lineage reprogramming is a new regenerative method to convert a matured cell into another cell including direct transdifferentiation without undergoing a pluripotent cell state and indirect transdifferentiation with an initial dedifferentiation-reversion (reprogramming) to a pluripotent cell state. Each cell type is quantified by a distinct valley on the potential landscape with higher probability. We investigated three driving forces for cell fate decision making: stochastic fluctuations, gene regulation and induction, which can lead to cell type switchings. We showed that under the driving forces the direct transdifferentiation process proceeds from a differentiated cell valley to another differentiated cell valley through either a distinct stable intermediate state or a certain series of unstable indeterminate states. The dedifferentiation process proceeds through a pluripotent cell state. Barrier height and the corresponding escape time from the valley on the landscape can be used to quantify the stability and efficiency of cell type switchings. We also uncovered the mechanisms of the underlying processes by quantifying the dominant biological paths of cell type switchings on the potential landscape. The dynamics of cell type switchings are determined by both landscape gradient and flux. The flux can lead to the deviations of the dominant biological paths for cell type switchings from the naively expected landscape gradient path. As a result, the corresponding dominant paths of cell type switchings are irreversible. We also classified the mechanisms of cell fate development from our landscape theory: super-critical pitchfork bifurcation, sub-critical pitchfork bifurcation, sub-critical pitchfork with two saddle-node bifurcation, and saddle-node bifurcation. Our model showed good agreements with the experiments. It provides a general framework to explore the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation. |
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Lineage reprogramming is a new regenerative method to convert a matured cell into another cell including direct transdifferentiation without undergoing a pluripotent cell state and indirect transdifferentiation with an initial dedifferentiation-reversion (reprogramming) to a pluripotent cell state. Each cell type is quantified by a distinct valley on the potential landscape with higher probability. We investigated three driving forces for cell fate decision making: stochastic fluctuations, gene regulation and induction, which can lead to cell type switchings. We showed that under the driving forces the direct transdifferentiation process proceeds from a differentiated cell valley to another differentiated cell valley through either a distinct stable intermediate state or a certain series of unstable indeterminate states. The dedifferentiation process proceeds through a pluripotent cell state. Barrier height and the corresponding escape time from the valley on the landscape can be used to quantify the stability and efficiency of cell type switchings. We also uncovered the mechanisms of the underlying processes by quantifying the dominant biological paths of cell type switchings on the potential landscape. The dynamics of cell type switchings are determined by both landscape gradient and flux. The flux can lead to the deviations of the dominant biological paths for cell type switchings from the naively expected landscape gradient path. As a result, the corresponding dominant paths of cell type switchings are irreversible. We also classified the mechanisms of cell fate development from our landscape theory: super-critical pitchfork bifurcation, sub-critical pitchfork bifurcation, sub-critical pitchfork with two saddle-node bifurcation, and saddle-node bifurcation. Our model showed good agreements with the experiments. It provides a general framework to explore the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0105216</identifier><identifier>PMID: 25133589</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Bifurcation theory ; Biology and Life Sciences ; Cell Dedifferentiation - physiology ; Cell Differentiation - physiology ; Cell fate ; Cell Transdifferentiation - physiology ; Cellular Reprogramming - physiology ; Chemistry ; Decision making ; Differentiation ; Fluctuations ; Flux ; Gene expression ; Gene regulation ; Genotype & phenotype ; Laboratories ; Models, Theoretical ; Noise control ; Physical Sciences ; Pluripotency ; Polypeptides ; Reversion ; Stem cells ; Stochasticity ; Valleys</subject><ispartof>PloS one, 2014-08, Vol.9 (8), p.e105216</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Xu et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://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>2014 Xu et al 2014 Xu et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-6e5eb9c0de692ab98db947ae91e0aa12033ecff9aaa1110cd2ad69d2b9881dd03</citedby><cites>FETCH-LOGICAL-c758t-6e5eb9c0de692ab98db947ae91e0aa12033ecff9aaa1110cd2ad69d2b9881dd03</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/PMC4136825/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4136825/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2926,23865,27923,27924,53790,53792,79371,79372</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25133589$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Loh, Yuin-Han</contributor><creatorcontrib>Xu, Li</creatorcontrib><creatorcontrib>Zhang, Kun</creatorcontrib><creatorcontrib>Wang, Jin</creatorcontrib><title>Exploring the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>We explored the underlying mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation (cell type switchings) from landscape and flux perspectives. Lineage reprogramming is a new regenerative method to convert a matured cell into another cell including direct transdifferentiation without undergoing a pluripotent cell state and indirect transdifferentiation with an initial dedifferentiation-reversion (reprogramming) to a pluripotent cell state. Each cell type is quantified by a distinct valley on the potential landscape with higher probability. We investigated three driving forces for cell fate decision making: stochastic fluctuations, gene regulation and induction, which can lead to cell type switchings. We showed that under the driving forces the direct transdifferentiation process proceeds from a differentiated cell valley to another differentiated cell valley through either a distinct stable intermediate state or a certain series of unstable indeterminate states. The dedifferentiation process proceeds through a pluripotent cell state. Barrier height and the corresponding escape time from the valley on the landscape can be used to quantify the stability and efficiency of cell type switchings. We also uncovered the mechanisms of the underlying processes by quantifying the dominant biological paths of cell type switchings on the potential landscape. The dynamics of cell type switchings are determined by both landscape gradient and flux. The flux can lead to the deviations of the dominant biological paths for cell type switchings from the naively expected landscape gradient path. As a result, the corresponding dominant paths of cell type switchings are irreversible. We also classified the mechanisms of cell fate development from our landscape theory: super-critical pitchfork bifurcation, sub-critical pitchfork bifurcation, sub-critical pitchfork with two saddle-node bifurcation, and saddle-node bifurcation. Our model showed good agreements with the experiments. It provides a general framework to explore the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation.</description><subject>Bifurcation theory</subject><subject>Biology and Life Sciences</subject><subject>Cell Dedifferentiation - physiology</subject><subject>Cell Differentiation - physiology</subject><subject>Cell fate</subject><subject>Cell Transdifferentiation - physiology</subject><subject>Cellular Reprogramming - physiology</subject><subject>Chemistry</subject><subject>Decision making</subject><subject>Differentiation</subject><subject>Fluctuations</subject><subject>Flux</subject><subject>Gene expression</subject><subject>Gene regulation</subject><subject>Genotype & phenotype</subject><subject>Laboratories</subject><subject>Models, Theoretical</subject><subject>Noise control</subject><subject>Physical Sciences</subject><subject>Pluripotency</subject><subject>Polypeptides</subject><subject>Reversion</subject><subject>Stem cells</subject><subject>Stochasticity</subject><subject>Valleys</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNk22L1DAQx4so3oN-A9GCcCi4a9ImbfNGOI5TFw4OfHobZpNJN0vbrEkr57c3dXvH9rwX0hdtpr_5T__TmSR5QcmS5iV9v3WD76BZ7lyHS0IJz2jxKDmmIs8WRUbyxwfPR8lJCFtCeF4VxdPkKOM0z3kljhNzebNrnLddnfYbTFtUG-hsaEPqTKqtMeix6y301nXvUo3_hDzuvKs9tO2oAZ1Oew9duMc9S54YaAI-n-6nyfePl98uPi-urj-tLs6vFqrkVb8okONaKKKxEBmsRaXXgpWAgiIBoNFJjsoYAfFAKVE6A10InUWyolqT_DR5tdeNpoKcWhQk5ZxlJeMZi8RqT2gHW7nztgX_Wzqw8m_A-VqC761qUHIey-sSNRGaMczWKAzlihIQRBSkjFofpmrDukWtol0PzUx0_qazG1m7X5LRvKgyHgXeTALe_Rww9LK1QWHTQIdu2H-3YISz0dnre-jD7iaqhmjAdsbFumoUleeMViwiVRWp5QNUvDS2VsV5MjbGZwlvZwmR6fGmr2EIQa6-fvl_9vrHnD07YDcITb8JrhnGkQlzkO1B5V0IHs1dkymR4zrcdkOO6yCndYhpLw9_0F3S7fznfwCivwe_</recordid><startdate>20140818</startdate><enddate>20140818</enddate><creator>Xu, Li</creator><creator>Zhang, Kun</creator><creator>Wang, Jin</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140818</creationdate><title>Exploring the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation</title><author>Xu, Li ; Zhang, Kun ; Wang, Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-6e5eb9c0de692ab98db947ae91e0aa12033ecff9aaa1110cd2ad69d2b9881dd03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Bifurcation theory</topic><topic>Biology and Life Sciences</topic><topic>Cell Dedifferentiation - physiology</topic><topic>Cell Differentiation - physiology</topic><topic>Cell fate</topic><topic>Cell Transdifferentiation - physiology</topic><topic>Cellular Reprogramming - physiology</topic><topic>Chemistry</topic><topic>Decision making</topic><topic>Differentiation</topic><topic>Fluctuations</topic><topic>Flux</topic><topic>Gene expression</topic><topic>Gene regulation</topic><topic>Genotype & phenotype</topic><topic>Laboratories</topic><topic>Models, Theoretical</topic><topic>Noise control</topic><topic>Physical Sciences</topic><topic>Pluripotency</topic><topic>Polypeptides</topic><topic>Reversion</topic><topic>Stem cells</topic><topic>Stochasticity</topic><topic>Valleys</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Li</creatorcontrib><creatorcontrib>Zhang, Kun</creatorcontrib><creatorcontrib>Wang, Jin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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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>Xu, Li</au><au>Zhang, Kun</au><au>Wang, Jin</au><au>Loh, Yuin-Han</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2014-08-18</date><risdate>2014</risdate><volume>9</volume><issue>8</issue><spage>e105216</spage><pages>e105216-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>We explored the underlying mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation (cell type switchings) from landscape and flux perspectives. Lineage reprogramming is a new regenerative method to convert a matured cell into another cell including direct transdifferentiation without undergoing a pluripotent cell state and indirect transdifferentiation with an initial dedifferentiation-reversion (reprogramming) to a pluripotent cell state. Each cell type is quantified by a distinct valley on the potential landscape with higher probability. We investigated three driving forces for cell fate decision making: stochastic fluctuations, gene regulation and induction, which can lead to cell type switchings. We showed that under the driving forces the direct transdifferentiation process proceeds from a differentiated cell valley to another differentiated cell valley through either a distinct stable intermediate state or a certain series of unstable indeterminate states. The dedifferentiation process proceeds through a pluripotent cell state. Barrier height and the corresponding escape time from the valley on the landscape can be used to quantify the stability and efficiency of cell type switchings. We also uncovered the mechanisms of the underlying processes by quantifying the dominant biological paths of cell type switchings on the potential landscape. The dynamics of cell type switchings are determined by both landscape gradient and flux. The flux can lead to the deviations of the dominant biological paths for cell type switchings from the naively expected landscape gradient path. As a result, the corresponding dominant paths of cell type switchings are irreversible. We also classified the mechanisms of cell fate development from our landscape theory: super-critical pitchfork bifurcation, sub-critical pitchfork bifurcation, sub-critical pitchfork with two saddle-node bifurcation, and saddle-node bifurcation. Our model showed good agreements with the experiments. It provides a general framework to explore the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25133589</pmid><doi>10.1371/journal.pone.0105216</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bifurcation theory Biology and Life Sciences Cell Dedifferentiation - physiology Cell Differentiation - physiology Cell fate Cell Transdifferentiation - physiology Cellular Reprogramming - physiology Chemistry Decision making Differentiation Fluctuations Flux Gene expression Gene regulation Genotype & phenotype Laboratories Models, Theoretical Noise control Physical Sciences Pluripotency Polypeptides Reversion Stem cells Stochasticity Valleys |
title | Exploring the mechanisms of differentiation, dedifferentiation, reprogramming and transdifferentiation |
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