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Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line
Rab7 regulates the biogenesis of late endosomes, lysosomes, and autophagosomes. It has been proposed that a functional and physical interaction exists between Rab7 and Rac1 GTPases in CDH1 endocytosis and ruffled border formation. In FRT cells over‐expressing Rab7, increased expression and activity...
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Published in: | Journal of cellular physiology 2016-08, Vol.231 (8), p.1695-1708 |
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container_title | Journal of cellular physiology |
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creator | Mascia, Anna Gentile, Flaviana Izzo, Antonella Mollo, Nunzia De Luca, Maria Bucci, Cecilia Nitsch, Lucio Calì, Gaetano |
description | Rab7 regulates the biogenesis of late endosomes, lysosomes, and autophagosomes. It has been proposed that a functional and physical interaction exists between Rab7 and Rac1 GTPases in CDH1 endocytosis and ruffled border formation. In FRT cells over‐expressing Rab7, increased expression and activity of Rac1 was observed, whereas a reduction of Rab7 expression by RNAi resulted in reduced Rac1 activity, as measured by PAK1 phosphorylation. We found that CDH1 endocytosis was extremely reduced only in Rab7 over‐expressing cells but was unchanged in Rab7 silenced cells. In Rab7 under or over‐expressing cells, Rab7 and LC3B‐II co‐localized and co‐localization in large circular structures occurred only in Rab7 over‐expressing cells. These large circular structures occurred in about 10% of the cell population; some of them (61%) showed co‐localization of Rab7 with cortactin and f‐actin and were identified as circular dorsal ruffles (CDRs), the others as mature autophagosomes. We propose that the over‐expression of Rab7 is sufficient to induce CDRs. Furthermore, in FRT cells, we found that the expression of the insoluble/active form of Rab7, rather than Rab5, or Rab8, was inducible by cAMP and that cAMP‐stimulated FRT cells showed increased PAK1 phosphorylation and were no longer able to endocytose CDH1. Finally, we demonstrated that Rab7 over‐expressing cells are able to endocytose exogenous thyroglobulin via pinocytosis/CDRs more efficiently than control cells. We propose that the major thyroglobulin endocytosis described in thyroid autonomous adenomas due to Rab7 increased expression, occurs via CDRs. J. Cell. Physiol. 231: 1695–1708, 2016. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/jcp.25267 |
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It has been proposed that a functional and physical interaction exists between Rab7 and Rac1 GTPases in CDH1 endocytosis and ruffled border formation. In FRT cells over‐expressing Rab7, increased expression and activity of Rac1 was observed, whereas a reduction of Rab7 expression by RNAi resulted in reduced Rac1 activity, as measured by PAK1 phosphorylation. We found that CDH1 endocytosis was extremely reduced only in Rab7 over‐expressing cells but was unchanged in Rab7 silenced cells. In Rab7 under or over‐expressing cells, Rab7 and LC3B‐II co‐localized and co‐localization in large circular structures occurred only in Rab7 over‐expressing cells. These large circular structures occurred in about 10% of the cell population; some of them (61%) showed co‐localization of Rab7 with cortactin and f‐actin and were identified as circular dorsal ruffles (CDRs), the others as mature autophagosomes. We propose that the over‐expression of Rab7 is sufficient to induce CDRs. Furthermore, in FRT cells, we found that the expression of the insoluble/active form of Rab7, rather than Rab5, or Rab8, was inducible by cAMP and that cAMP‐stimulated FRT cells showed increased PAK1 phosphorylation and were no longer able to endocytose CDH1. Finally, we demonstrated that Rab7 over‐expressing cells are able to endocytose exogenous thyroglobulin via pinocytosis/CDRs more efficiently than control cells. We propose that the major thyroglobulin endocytosis described in thyroid autonomous adenomas due to Rab7 increased expression, occurs via CDRs. J. Cell. Physiol. 231: 1695–1708, 2016. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.25267</identifier><identifier>PMID: 26599499</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Actins - metabolism ; Animals ; Autophagy ; Cadherins - metabolism ; Cell Line ; Cell Surface Extensions - drug effects ; Cell Surface Extensions - enzymology ; Cortactin - metabolism ; Cyclic AMP - metabolism ; Endocytosis - drug effects ; Microtubule-Associated Proteins - metabolism ; p21-Activated Kinases - metabolism ; Phosphorylation ; Pinocytosis ; rab GTP-Binding Proteins - genetics ; rab GTP-Binding Proteins - metabolism ; rac1 GTP-Binding Protein - metabolism ; Rats, Inbred F344 ; RNA Interference ; Second Messenger Systems ; Thyroglobulin - metabolism ; Thyroid ; Thyroid Gland - cytology ; Thyroid Gland - drug effects ; Thyroid Gland - enzymology ; Time Factors ; Transfection ; Vacuoles - drug effects ; Vacuoles - enzymology</subject><ispartof>Journal of cellular physiology, 2016-08, Vol.231 (8), p.1695-1708</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3927-84e4e58b1764a29a6acbfe5bee01f76e771d1274b5fff9387e17b4be87a091ee3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26599499$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mascia, Anna</creatorcontrib><creatorcontrib>Gentile, Flaviana</creatorcontrib><creatorcontrib>Izzo, Antonella</creatorcontrib><creatorcontrib>Mollo, Nunzia</creatorcontrib><creatorcontrib>De Luca, Maria</creatorcontrib><creatorcontrib>Bucci, Cecilia</creatorcontrib><creatorcontrib>Nitsch, Lucio</creatorcontrib><creatorcontrib>Calì, Gaetano</creatorcontrib><title>Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line</title><title>Journal of cellular physiology</title><addtitle>J. Cell. Physiol</addtitle><description>Rab7 regulates the biogenesis of late endosomes, lysosomes, and autophagosomes. It has been proposed that a functional and physical interaction exists between Rab7 and Rac1 GTPases in CDH1 endocytosis and ruffled border formation. In FRT cells over‐expressing Rab7, increased expression and activity of Rac1 was observed, whereas a reduction of Rab7 expression by RNAi resulted in reduced Rac1 activity, as measured by PAK1 phosphorylation. We found that CDH1 endocytosis was extremely reduced only in Rab7 over‐expressing cells but was unchanged in Rab7 silenced cells. In Rab7 under or over‐expressing cells, Rab7 and LC3B‐II co‐localized and co‐localization in large circular structures occurred only in Rab7 over‐expressing cells. These large circular structures occurred in about 10% of the cell population; some of them (61%) showed co‐localization of Rab7 with cortactin and f‐actin and were identified as circular dorsal ruffles (CDRs), the others as mature autophagosomes. We propose that the over‐expression of Rab7 is sufficient to induce CDRs. Furthermore, in FRT cells, we found that the expression of the insoluble/active form of Rab7, rather than Rab5, or Rab8, was inducible by cAMP and that cAMP‐stimulated FRT cells showed increased PAK1 phosphorylation and were no longer able to endocytose CDH1. Finally, we demonstrated that Rab7 over‐expressing cells are able to endocytose exogenous thyroglobulin via pinocytosis/CDRs more efficiently than control cells. We propose that the major thyroglobulin endocytosis described in thyroid autonomous adenomas due to Rab7 increased expression, occurs via CDRs. J. Cell. Physiol. 231: 1695–1708, 2016. © 2015 Wiley Periodicals, Inc.</description><subject>Actins - metabolism</subject><subject>Animals</subject><subject>Autophagy</subject><subject>Cadherins - metabolism</subject><subject>Cell Line</subject><subject>Cell Surface Extensions - drug effects</subject><subject>Cell Surface Extensions - enzymology</subject><subject>Cortactin - metabolism</subject><subject>Cyclic AMP - metabolism</subject><subject>Endocytosis - drug effects</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>p21-Activated Kinases - metabolism</subject><subject>Phosphorylation</subject><subject>Pinocytosis</subject><subject>rab GTP-Binding Proteins - genetics</subject><subject>rab GTP-Binding Proteins - metabolism</subject><subject>rac1 GTP-Binding Protein - metabolism</subject><subject>Rats, Inbred F344</subject><subject>RNA Interference</subject><subject>Second Messenger Systems</subject><subject>Thyroglobulin - metabolism</subject><subject>Thyroid</subject><subject>Thyroid Gland - cytology</subject><subject>Thyroid Gland - drug effects</subject><subject>Thyroid Gland - enzymology</subject><subject>Time Factors</subject><subject>Transfection</subject><subject>Vacuoles - drug effects</subject><subject>Vacuoles - enzymology</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpdkUFv1DAQhS0EokvhwB9AlrhwIK3txHF8RGm7LawAbYt6tOxkUrx47a2dCLa_Hu9u6YGTR37fG83MQ-gtJSeUEHa66jYnjLNaPEMzSqQoqpqz52iWNVpIXtEj9CqlFSFEyrJ8iY5YzaWspJyhh6U2Ai_hbnJ6hITbs0uKz30fuu0Ykk0fcWtjl8WIz0JM2uHlNAwuk3PwsAe07_HNz20Mdy6YyVmPr_wI0WtnH_Rog8f5Sx8Q2-MWnMML6-E1ejFol-DN43uMflyc37SXxeLb_Kr9tCi6UjJRNBVUwBtDRV1pJnWtOzMANwCEDqIGIWhPmagMH4ZBlo0AKkxloBGaSApQHqMPh76bGO4nSKNa29TlKbSHMCVFRcOaktSCZPT9f-gqTLtN9hTlTNTNjnr3SE1mDb3aRLvWcav-XTUDpwfgt3WwfdIpUbu4VI5L7eNSn9vv-yI7ioPDphH-PDl0_KWyKri6_TpXze31l4vyulS8_AuN9ZXy</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Mascia, Anna</creator><creator>Gentile, Flaviana</creator><creator>Izzo, Antonella</creator><creator>Mollo, Nunzia</creator><creator>De Luca, Maria</creator><creator>Bucci, Cecilia</creator><creator>Nitsch, Lucio</creator><creator>Calì, Gaetano</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>201608</creationdate><title>Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line</title><author>Mascia, Anna ; 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Cell. Physiol</addtitle><date>2016-08</date><risdate>2016</risdate><volume>231</volume><issue>8</issue><spage>1695</spage><epage>1708</epage><pages>1695-1708</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Rab7 regulates the biogenesis of late endosomes, lysosomes, and autophagosomes. It has been proposed that a functional and physical interaction exists between Rab7 and Rac1 GTPases in CDH1 endocytosis and ruffled border formation. In FRT cells over‐expressing Rab7, increased expression and activity of Rac1 was observed, whereas a reduction of Rab7 expression by RNAi resulted in reduced Rac1 activity, as measured by PAK1 phosphorylation. We found that CDH1 endocytosis was extremely reduced only in Rab7 over‐expressing cells but was unchanged in Rab7 silenced cells. In Rab7 under or over‐expressing cells, Rab7 and LC3B‐II co‐localized and co‐localization in large circular structures occurred only in Rab7 over‐expressing cells. These large circular structures occurred in about 10% of the cell population; some of them (61%) showed co‐localization of Rab7 with cortactin and f‐actin and were identified as circular dorsal ruffles (CDRs), the others as mature autophagosomes. We propose that the over‐expression of Rab7 is sufficient to induce CDRs. Furthermore, in FRT cells, we found that the expression of the insoluble/active form of Rab7, rather than Rab5, or Rab8, was inducible by cAMP and that cAMP‐stimulated FRT cells showed increased PAK1 phosphorylation and were no longer able to endocytose CDH1. Finally, we demonstrated that Rab7 over‐expressing cells are able to endocytose exogenous thyroglobulin via pinocytosis/CDRs more efficiently than control cells. We propose that the major thyroglobulin endocytosis described in thyroid autonomous adenomas due to Rab7 increased expression, occurs via CDRs. J. Cell. Physiol. 231: 1695–1708, 2016. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26599499</pmid><doi>10.1002/jcp.25267</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - metabolism Animals Autophagy Cadherins - metabolism Cell Line Cell Surface Extensions - drug effects Cell Surface Extensions - enzymology Cortactin - metabolism Cyclic AMP - metabolism Endocytosis - drug effects Microtubule-Associated Proteins - metabolism p21-Activated Kinases - metabolism Phosphorylation Pinocytosis rab GTP-Binding Proteins - genetics rab GTP-Binding Proteins - metabolism rac1 GTP-Binding Protein - metabolism Rats, Inbred F344 RNA Interference Second Messenger Systems Thyroglobulin - metabolism Thyroid Thyroid Gland - cytology Thyroid Gland - drug effects Thyroid Gland - enzymology Time Factors Transfection Vacuoles - drug effects Vacuoles - enzymology |
title | Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line |
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