Rab7 Regulates CDH1 Endocytosis, Circular Dorsal Ruffles Genesis, and Thyroglobulin Internalization in a Thyroid Cell Line

J Cell Physiol. 2016 Aug;231(8):1695-708. doi: 10.1002/jcp.25267. Epub 2015 Dec 10.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 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
  • Phosphorylation
  • Pinocytosis
  • RNA Interference
  • Rats, Inbred F344
  • Second Messenger Systems
  • Thyroglobulin / metabolism*
  • Thyroid Gland / cytology
  • Thyroid Gland / drug effects
  • Thyroid Gland / enzymology*
  • Time Factors
  • Transfection
  • Vacuoles / drug effects
  • Vacuoles / enzymology*
  • p21-Activated Kinases / metabolism
  • rab GTP-Binding Proteins / genetics
  • rab GTP-Binding Proteins / metabolism*
  • rab7 GTP-Binding Proteins
  • rac1 GTP-Binding Protein / metabolism

Substances

  • Actins
  • CDH1 protein, rat
  • Cadherins
  • Cortactin
  • LC3 protein, rat
  • Microtubule-Associated Proteins
  • rab7 GTP-Binding Proteins
  • rab7 GTP-binding proteins, rat
  • Thyroglobulin
  • Cyclic AMP
  • Pak1 protein, rat
  • p21-Activated Kinases
  • Rac1 protein, rat
  • rab GTP-Binding Proteins
  • rac1 GTP-Binding Protein