Reggies/flotillins interact with Rab11a and SNX4 at the tubulo-vesicular recycling compartment and function in transferrin receptor and E-cadherin trafficking

Solis, Gonzalo P.; Hülsbusch, Nikola; Radon, Yvonne; Katanaev, Vladimir L.; Plattner, Helmut; Stürmer, Claudia

Reggies/flotillins interact with Rab11a and SNX4 at the tubulo-vesicular recycling compartment and function in transferrin receptor and E-cadherin trafficking

Dateien

Solis_240152.pdfGröße: 3.66 MBDownloads: 284

Datum

2013

Autor:innen

Solis, Gonzalo P.

Hülsbusch, Nikola

Radon, Yvonne

Katanaev, Vladimir L.

Plattner, Helmut

Stürmer, Claudia

Open Access-Veröffentlichung

Open Access Green

Sammlungen

Biologie

Publikationstyp

Zeitschriftenartikel

Publikationsstatus

Published

Erschienen in

Molecular Biology of the Cell. 2013, 24(17), pp. 2689-2702. ISSN 1059-1524. eISSN 1939-4586. Available under: doi: 10.1091/mbc.E12-12-0854

Zusammenfassung

The lipid raft proteins reggie-1 and -2 (flotillins) were implicated in membrane protein trafficking but exactly how has remained elusive. We discovered that reggie-1 and -2 associate with the Rab11a, SNX4 and EHD1 decorated tubulo-vesicular recycling compartment in HeLa cells and that reggie-1 directly interacts with Rab11a and SNX4. shRNA-mediated down-regulation of reggie-1 (and -2) in HeLa cells reduced the association of Rab11a with tubular structures and impaired the recycling of the transferrin (Tf)-transferrin receptor (TfR) complex to the plasma membrane. Overexpression of constitutive-active Rab11a rescued TfR recycling in reggie-deficient HeLa cells. Likewise, in a Ca2+ switch assay in reggie-depleted A431 cells, internalized E-cadherin was not efficiently recycled to the plasma membrane upon Ca2+ repletion. However, E-cadherin recycling was rescued by overexpression of constitutive-active Rab11a or SNX4 in reggie-deficient A431 cells. This suggests that the function of reggie-1 in sorting and recycling occurs in association with Rab11a and SNX4. Interestingly, impaired recycling in reggie-deficient cells led to de novo E-cadherin biosynthesis and cell contact reformation, showing that cells have ways to compensate the loss of reggies. Together our results identify reggie-1 as a regulator of the Rab11a/SNX4-controlled sorting and recycling pathway which is -like reggies- evolutionarily conserved.

Fachgebiet (DDC)

570 Biowissenschaften, Biologie

Zitieren

ISO 690

SOLIS, Gonzalo P., Nikola HÜLSBUSCH, Yvonne RADON, Vladimir L. KATANAEV, Helmut PLATTNER, Claudia STÜRMER, 2013. Reggies/flotillins interact with Rab11a and SNX4 at the tubulo-vesicular recycling compartment and function in transferrin receptor and E-cadherin trafficking. In: Molecular Biology of the Cell. 2013, 24(17), pp. 2689-2702. ISSN 1059-1524. eISSN 1939-4586. Available under: doi: 10.1091/mbc.E12-12-0854

BibTex

@article{Solis2013-09Reggi-24015,
  year={2013},
  doi={10.1091/mbc.E12-12-0854},
  title={Reggies/flotillins interact with Rab11a and SNX4 at the tubulo-vesicular recycling compartment and function in transferrin receptor and E-cadherin trafficking},
  number={17},
  volume={24},
  issn={1059-1524},
  journal={Molecular Biology of the Cell},
  pages={2689--2702},
  author={Solis, Gonzalo P. and Hülsbusch, Nikola and Radon, Yvonne and Katanaev, Vladimir L. and Plattner, Helmut and Stürmer, Claudia}
}

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Universitätsbibliographie

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