Cellular electroporation induces dedifferentiation in intact newt limbs
Newts have the remarkable ability to regenerate lost appendages including their forelimbs, hindlimbs, and tails. Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane be...
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Veröffentlicht in: | Developmental biology 2006-11, Vol.299 (1), p.257-271 |
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creator | Atkinson, Donald L. Stevenson, Tamara J. Park, Eon Joo Riedy, Matthew D. Milash, Brett Odelberg, Shannon J. |
description | Newts have the remarkable ability to regenerate lost appendages including their forelimbs, hindlimbs, and tails. Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane begin to dedifferentiate to form a pool of proliferating progenitor cells known as the regeneration blastema. We show that dedifferentiation of internal appendage cells can be initiated in the absence of amputation by applying an electric field sufficient to induce cellular electroporation, but not necrosis or apoptosis. The time course for dedifferentiation following electroporation is similar to that observed following amputation with evidence of dedifferentiation beginning at about 5 days postelectroporation and continuing for 2 to 3 weeks. Microarray analyses, real-time RT-PCR, and in situ hybridization show that changes in early gene expression are similar following amputation or electroporation. We conclude that the application of an electric field sufficient to induce transient electroporation of cell membranes induces a dedifferentiation response that is virtually indistinguishable from the response that occurs following amputation of newt appendages. This discovery allows dedifferentiation to be studied in the absence of wound healing and may aid in identifying genes required for cellular plasticity. |
doi_str_mv | 10.1016/j.ydbio.2006.07.027 |
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Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane begin to dedifferentiate to form a pool of proliferating progenitor cells known as the regeneration blastema. We show that dedifferentiation of internal appendage cells can be initiated in the absence of amputation by applying an electric field sufficient to induce cellular electroporation, but not necrosis or apoptosis. The time course for dedifferentiation following electroporation is similar to that observed following amputation with evidence of dedifferentiation beginning at about 5 days postelectroporation and continuing for 2 to 3 weeks. Microarray analyses, real-time RT-PCR, and in situ hybridization show that changes in early gene expression are similar following amputation or electroporation. We conclude that the application of an electric field sufficient to induce transient electroporation of cell membranes induces a dedifferentiation response that is virtually indistinguishable from the response that occurs following amputation of newt appendages. This discovery allows dedifferentiation to be studied in the absence of wound healing and may aid in identifying genes required for cellular plasticity.</description><identifier>ISSN: 0012-1606</identifier><identifier>EISSN: 1095-564X</identifier><identifier>DOI: 10.1016/j.ydbio.2006.07.027</identifier><identifier>PMID: 16949563</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Amputation ; Animals ; Cell Cycle ; Cell Death ; Cell Differentiation ; Cellular plasticity ; Dedifferentiation ; Electric field ; Electroporation ; Electroporation - methods ; Forelimb - cytology ; Forelimb - physiology ; Gene Expression Profiling ; Gene Expression Regulation ; Hindlimb - cytology ; Newt ; Notophthalmus viridescens ; Regeneration ; Salamandridae ; Salamandridae - physiology ; Tail - cytology ; Time Factors</subject><ispartof>Developmental biology, 2006-11, Vol.299 (1), p.257-271</ispartof><rights>2006 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-2202d49fa79aad83753f8c409bba0f4465df22c6c0adb95c9766b2bda15744de3</citedby><cites>FETCH-LOGICAL-c488t-2202d49fa79aad83753f8c409bba0f4465df22c6c0adb95c9766b2bda15744de3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0012160606010323$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16949563$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Atkinson, Donald L.</creatorcontrib><creatorcontrib>Stevenson, Tamara J.</creatorcontrib><creatorcontrib>Park, Eon Joo</creatorcontrib><creatorcontrib>Riedy, Matthew D.</creatorcontrib><creatorcontrib>Milash, Brett</creatorcontrib><creatorcontrib>Odelberg, Shannon J.</creatorcontrib><title>Cellular electroporation induces dedifferentiation in intact newt limbs</title><title>Developmental biology</title><addtitle>Dev Biol</addtitle><description>Newts have the remarkable ability to regenerate lost appendages including their forelimbs, hindlimbs, and tails. Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane begin to dedifferentiate to form a pool of proliferating progenitor cells known as the regeneration blastema. We show that dedifferentiation of internal appendage cells can be initiated in the absence of amputation by applying an electric field sufficient to induce cellular electroporation, but not necrosis or apoptosis. The time course for dedifferentiation following electroporation is similar to that observed following amputation with evidence of dedifferentiation beginning at about 5 days postelectroporation and continuing for 2 to 3 weeks. Microarray analyses, real-time RT-PCR, and in situ hybridization show that changes in early gene expression are similar following amputation or electroporation. We conclude that the application of an electric field sufficient to induce transient electroporation of cell membranes induces a dedifferentiation response that is virtually indistinguishable from the response that occurs following amputation of newt appendages. This discovery allows dedifferentiation to be studied in the absence of wound healing and may aid in identifying genes required for cellular plasticity.</description><subject>Amputation</subject><subject>Animals</subject><subject>Cell Cycle</subject><subject>Cell Death</subject><subject>Cell Differentiation</subject><subject>Cellular plasticity</subject><subject>Dedifferentiation</subject><subject>Electric field</subject><subject>Electroporation</subject><subject>Electroporation - methods</subject><subject>Forelimb - cytology</subject><subject>Forelimb - physiology</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation</subject><subject>Hindlimb - cytology</subject><subject>Newt</subject><subject>Notophthalmus viridescens</subject><subject>Regeneration</subject><subject>Salamandridae</subject><subject>Salamandridae - physiology</subject><subject>Tail - cytology</subject><subject>Time Factors</subject><issn>0012-1606</issn><issn>1095-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQQC1URJeFX1AJ5dRbwthx_HEoElpBQarEBSRulmNPilfZeGsnrfrvcdkthQtIluYwb8Yz8wg5o9BQoOLttrn3fYgNAxANyAaYfEZWFHRXd4J_PyErAMpqKkCckpc5bwGgVap9QU6p0Fx3ol2Ryw2O4zLaVOGIbk5xH5OdQ5yqMPnFYa48-jAMmHCaw2OmvNm6uZrwbq7GsOvzK_J8sGPG18e4Jt8-fvi6-VRffbn8vHl_VTuu1FwzBsxzPViprfWqlV07KMdB972FgXPR-YExJxxY3-vOaSlEz3pvaSc599iuybtD3_3S79C7MlWyo9mnsLPp3kQbzN-ZKfww1_HWUKkoKyuvyfmxQYo3C-bZ7EJ25Qh2wrhkI5QWoNj_QarbDpRUBWwPoEsx54TD72komAdTZmt-mTIPpgxIU0yVqjd_LvJUc1RTgIsDgOWctwGTyS7g5IqOVEwZH8M_P_gJgRGoZw</recordid><startdate>20061101</startdate><enddate>20061101</enddate><creator>Atkinson, Donald L.</creator><creator>Stevenson, Tamara J.</creator><creator>Park, Eon Joo</creator><creator>Riedy, Matthew D.</creator><creator>Milash, Brett</creator><creator>Odelberg, Shannon J.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>7QP</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20061101</creationdate><title>Cellular electroporation induces dedifferentiation in intact newt limbs</title><author>Atkinson, Donald L. ; Stevenson, Tamara J. ; Park, Eon Joo ; Riedy, Matthew D. ; Milash, Brett ; Odelberg, Shannon J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-2202d49fa79aad83753f8c409bba0f4465df22c6c0adb95c9766b2bda15744de3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Amputation</topic><topic>Animals</topic><topic>Cell Cycle</topic><topic>Cell Death</topic><topic>Cell Differentiation</topic><topic>Cellular plasticity</topic><topic>Dedifferentiation</topic><topic>Electric field</topic><topic>Electroporation</topic><topic>Electroporation - methods</topic><topic>Forelimb - cytology</topic><topic>Forelimb - physiology</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation</topic><topic>Hindlimb - cytology</topic><topic>Newt</topic><topic>Notophthalmus viridescens</topic><topic>Regeneration</topic><topic>Salamandridae</topic><topic>Salamandridae - physiology</topic><topic>Tail - cytology</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atkinson, Donald L.</creatorcontrib><creatorcontrib>Stevenson, Tamara J.</creatorcontrib><creatorcontrib>Park, Eon Joo</creatorcontrib><creatorcontrib>Riedy, Matthew D.</creatorcontrib><creatorcontrib>Milash, Brett</creatorcontrib><creatorcontrib>Odelberg, Shannon J.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Developmental biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atkinson, Donald L.</au><au>Stevenson, Tamara J.</au><au>Park, Eon Joo</au><au>Riedy, Matthew D.</au><au>Milash, Brett</au><au>Odelberg, Shannon J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cellular electroporation induces dedifferentiation in intact newt limbs</atitle><jtitle>Developmental biology</jtitle><addtitle>Dev Biol</addtitle><date>2006-11-01</date><risdate>2006</risdate><volume>299</volume><issue>1</issue><spage>257</spage><epage>271</epage><pages>257-271</pages><issn>0012-1606</issn><eissn>1095-564X</eissn><abstract>Newts have the remarkable ability to regenerate lost appendages including their forelimbs, hindlimbs, and tails. Following amputation of an appendage, the wound is rapidly closed by the migration of epithelial cells from the proximal epidermis. Internal cells just proximal to the amputation plane begin to dedifferentiate to form a pool of proliferating progenitor cells known as the regeneration blastema. We show that dedifferentiation of internal appendage cells can be initiated in the absence of amputation by applying an electric field sufficient to induce cellular electroporation, but not necrosis or apoptosis. The time course for dedifferentiation following electroporation is similar to that observed following amputation with evidence of dedifferentiation beginning at about 5 days postelectroporation and continuing for 2 to 3 weeks. Microarray analyses, real-time RT-PCR, and in situ hybridization show that changes in early gene expression are similar following amputation or electroporation. We conclude that the application of an electric field sufficient to induce transient electroporation of cell membranes induces a dedifferentiation response that is virtually indistinguishable from the response that occurs following amputation of newt appendages. This discovery allows dedifferentiation to be studied in the absence of wound healing and may aid in identifying genes required for cellular plasticity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16949563</pmid><doi>10.1016/j.ydbio.2006.07.027</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amputation Animals Cell Cycle Cell Death Cell Differentiation Cellular plasticity Dedifferentiation Electric field Electroporation Electroporation - methods Forelimb - cytology Forelimb - physiology Gene Expression Profiling Gene Expression Regulation Hindlimb - cytology Newt Notophthalmus viridescens Regeneration Salamandridae Salamandridae - physiology Tail - cytology Time Factors |
title | Cellular electroporation induces dedifferentiation in intact newt limbs |
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