Literature DB >> 7775571

Apical and basolateral coated pits of MDCK cells differ in their rates of maturation into coated vesicles, but not in the ability to distinguish between mutant hemagglutinin proteins with different internalization signals.

H Y Naim1, D T Dodds, C B Brewer, M G Roth.   

Abstract

In polarized epithelial MDCK cells, all known endogenous endocytic receptors are found on the basolateral domain. The influenza virus hemagglutinin (HA) which is normally sorted to the apical plasma membrane, can be converted to a basolateral protein by specific mutations in its short cytoplasmic domain that also create internalization signals. For some of these mutations, sorting to the basolateral surface is incomplete, allowing internalization of two proteins that differ by a single amino acid of the internalization signal to be compared at both the apical and basolateral surfaces of MDCK cells. The rates of internalization of HA-Y543 and HA-Y543,R546 from the basolateral surface of polarized MDCK cells resembled those in nonpolarized cells, whereas their rates of internalization from the apical cell surface were fivefold slower. However, HA-Y543,R546 was internalized approximately threefold faster than HA-Y543 at both membrane domains, indicating that apical endocytic pits in polarized MDCK cells retained the ability to discriminate between different internalization signals. Slower internalization from the apical surface could not be explained by a limiting number of coated pits: apical membrane contained 0.7 as many coated pits per cell cross-section as did basolateral membranes. 10-14% of HA-Y543 at the apical surface of polarized MDCK cells was found in coated pits, a percentage not significantly different from that observed in apical coated pits of nonpolarized MDCK cells, where internalization was fivefold faster. Thus, there was no lack of binding sites for HA-Y543 in apical coated pits of polarized cells. However, at the apical surface many more shallow pits, and fewer deep, mature pits, were observed than were seen at the basolateral. These results suggest that the slower internalization at the apical surface is due to slower maturation of coated pits, and not to a difference in recognition of internalization signals.

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Year:  1995        PMID: 7775571      PMCID: PMC2120466          DOI: 10.1083/jcb.129.5.1241

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  30 in total

1.  A mutation that impairs the ability of lipoprotein receptors to localise in coated pits on the cell surface of human fibroblasts.

Authors:  R G Anderson; J L Goldstein; M S Brown
Journal:  Nature       Date:  1977 Dec 22-29       Impact factor: 49.962

2.  Rapid and efficient site-specific mutagenesis without phenotypic selection.

Authors:  T A Kunkel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

3.  A single amino acid change in the cytoplasmic domain allows the influenza virus hemagglutinin to be endocytosed through coated pits.

Authors:  J Lazarovits; M Roth
Journal:  Cell       Date:  1988-06-03       Impact factor: 41.582

4.  Inhibition of apical but not basolateral endocytosis of ricin and folate in Caco-2 cells by cytochalasin D.

Authors:  M R Jackman; W Shurety; J A Ellis; J P Luzio
Journal:  J Cell Sci       Date:  1994-09       Impact factor: 5.285

5.  Meeting of the apical and basolateral endocytic pathways of the Madin-Darby canine kidney cell in late endosomes.

Authors:  R G Parton; K Prydz; M Bomsel; K Simons; G Griffiths
Journal:  J Cell Biol       Date:  1989-12       Impact factor: 10.539

6.  A quantitative analysis of the endocytic pathway in baby hamster kidney cells.

Authors:  G Griffiths; R Back; M Marsh
Journal:  J Cell Biol       Date:  1989-12       Impact factor: 10.539

7.  Hypertonic media inhibit receptor-mediated endocytosis by blocking clathrin-coated pit formation.

Authors:  J E Heuser; R G Anderson
Journal:  J Cell Biol       Date:  1989-02       Impact factor: 10.539

8.  Endocytosis in filter-grown Madin-Darby canine kidney cells.

Authors:  M Bomsel; K Prydz; R G Parton; J Gruenberg; K Simons
Journal:  J Cell Biol       Date:  1989-12       Impact factor: 10.539

9.  Characteristics of the tyrosine recognition signal for internalization of transmembrane surface glycoproteins.

Authors:  N T Ktistakis; D Thomas; M G Roth
Journal:  J Cell Biol       Date:  1990-10       Impact factor: 10.539

10.  Mutagenesis of the human transferrin receptor: two cytoplasmic phenylalanines are required for efficient internalization and a second-site mutation is capable of reverting an internalization-defective phenotype.

Authors:  T E McGraw; B Pytowski; J Arzt; C Ferrone
Journal:  J Cell Biol       Date:  1991-03       Impact factor: 10.539

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  13 in total

1.  Actin is required for endocytosis at the apical surface of Madin-Darby canine kidney cells where ARF6 and clathrin regulate the actin cytoskeleton.

Authors:  Tehila Hyman; Miri Shmuel; Yoram Altschuler
Journal:  Mol Biol Cell       Date:  2005-10-26       Impact factor: 4.138

2.  In vitro binding of clathrin adaptors to sorting signals correlates with endocytosis and basolateral sorting.

Authors:  R Heilker; U Manning-Krieg; J F Zuber; M Spiess
Journal:  EMBO J       Date:  1996-06-03       Impact factor: 11.598

3.  Constitutive internalization of cystic fibrosis transmembrane conductance regulator occurs via clathrin-dependent endocytosis and is regulated by protein phosphorylation.

Authors:  G L Lukacs; G Segal; N Kartner; S Grinstein; F Zhang
Journal:  Biochem J       Date:  1997-12-01       Impact factor: 3.857

Review 4.  Sorting it out in endosomes: an emerging concept in renal epithelial cell transport regulation.

Authors:  Paul A Welling; Ora A Weisz
Journal:  Physiology (Bethesda)       Date:  2010-10

5.  Apical and basolateral endosomes of MDCK cells are interconnected and contain a polarized sorting mechanism.

Authors:  G Odorizzi; A Pearse; D Domingo; I S Trowbridge; C R Hopkins
Journal:  J Cell Biol       Date:  1996-10       Impact factor: 10.539

6.  Induction of caveolae in the apical plasma membrane of Madin-Darby canine kidney cells.

Authors:  P Verkade; T Harder; F Lafont; K Simons
Journal:  J Cell Biol       Date:  2000-02-21       Impact factor: 10.539

7.  N-Glycans mediate the apical sorting of a GPI-anchored, raft-associated protein in Madin-Darby canine kidney cells.

Authors:  J H Benting; A G Rietveld; K Simons
Journal:  J Cell Biol       Date:  1999-07-26       Impact factor: 10.539

8.  ADP-ribosylation factor 6 and endocytosis at the apical surface of Madin-Darby canine kidney cells.

Authors:  Y Altschuler; S Liu; L Katz; K Tang; S Hardy; F Brodsky; G Apodaca; K Mostov
Journal:  J Cell Biol       Date:  1999-10-04       Impact factor: 10.539

9.  Dynamin:GTP controls the formation of constricted coated pits, the rate limiting step in clathrin-mediated endocytosis.

Authors:  S Sever; H Damke; S L Schmid
Journal:  J Cell Biol       Date:  2000-09-04       Impact factor: 10.539

10.  PIP5KIβ selectively modulates apical endocytosis in polarized renal epithelial cells.

Authors:  Christina M Szalinski; Christopher J Guerriero; Wily G Ruiz; Brianne E Docter; Youssef Rbaibi; Núria M Pastor-Soler; Gerard Apodaca; Manojkumar A Puthenveedu; Ora A Weisz
Journal:  PLoS One       Date:  2013-01-16       Impact factor: 3.240

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