Literature DB >> 8138568

IFAP 300 is common to desmosomes and hemidesmosomes and is a possible linker of intermediate filaments to these junctions.

O Skalli1, J C Jones, R Gagescu, R D Goldman.   

Abstract

The distribution of IFAP 300, a protein previously characterized as cross-linking vimentin intermediate filaments (IF), has been investigated in epithelial cells. In frozen sections of bovine tongue epithelium the staining obtained with IFAP 300 antibodies is concentrated in the peripheral cytoplasm of keratinocytes, including the entire peripheral region of basal cells. Further immunofluorescence studies reveal that in primary cultures of mouse keratinocytes the distribution of IFAP 300 is similar to that of the desmosomal protein desmoplakin. In rat bladder carcinoma 804G cells the staining pattern of IFAP 300 antibodies coincides with that obtained with antibodies against the hemidesmosomal protein BP 230. By immunogold electron microscopy IFAP 300 is mainly located at sites where IF appear to attach to desmosomes and hemidesmosomes. Morphometric analyses of the distribution of the gold particles show that IFAP 300 overlaps with desmoplakin and BP 230, but also that it extends deeper into the cytoplasm than these latter two proteins. The staining reaction seen in epithelial cells by immunofluorescence and immunogold is specific for IFAP 300 as shown by immunoblotting. Immunoblotting also reveals that IFAP 300 is present in both cell-free preparations of desmosomes and hemidesmosomes. These morphological and biochemical results are intriguing since, in recent years, the proteins appearing in these two types of junctions have been found to be different. One possible exception is plectin, a protein that has been suggested to be very similar to IFAP 300. However, we show here that IFAP 300 differs from plectin in several respects, including differences at the primary sequence level. We also show that purified IFAP 300 pellets with in vitro polymerized IF prepared from desmosome-associated keratins under conditions in which IFAP 300 alone is not sedimentable. This indicates that IFAP 300 can associate with keratin IF. These data, taken together with the immunogold results, suggest that IFAP 300 functions in epithelial cells as a linker protein connecting IF to desmosomes as well as to hemidesmosomes, possibly through structurally related proteins such as desmoplakin and BP 230, respectively.

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Year:  1994        PMID: 8138568      PMCID: PMC2120004          DOI: 10.1083/jcb.125.1.159

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


  62 in total

1.  Cell cycle-dependent changes in the organization of an intermediate filament-associated protein: correlation with phosphorylation by p34cdc2.

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3.  Efficient isolation of genes by using antibody probes.

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Authors:  G Wiche; M A Baker
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5.  Production of rabbit antibodies against carboxy-terminal epitopes encoded by bullous pemphigoid cDNA.

Authors:  T Tanaka; N J Korman; H Shimizu; R A Eady; V Klaus-Kovtun; K Cehrs; J R Stanley
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6.  A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering.

Authors:  E B Lane; E L Rugg; H Navsaria; I M Leigh; A H Heagerty; A Ishida-Yamamoto; R A Eady
Journal:  Nature       Date:  1992-03-19       Impact factor: 49.962

7.  Identification of a new hemidesmosomal protein, HD1: a major, high molecular mass component of isolated hemidesmosomes.

Authors:  Y Hieda; Y Nishizawa; J Uematsu; K Owaribe
Journal:  J Cell Biol       Date:  1992-03       Impact factor: 10.539

8.  A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases.

Authors:  P A Coulombe; M E Hutton; R Vassar; E Fuchs
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

9.  A 300,000-mol-wt intermediate filament-associated protein in baby hamster kidney (BHK-21) cells.

Authors:  H Y Yang; N Lieska; A E Goldman; R D Goldman
Journal:  J Cell Biol       Date:  1985-02       Impact factor: 10.539

10.  Purification of the 300K intermediate filament-associated protein and its in vitro recombination with intermediate filaments.

Authors:  N Lieska; H Y Yang; R D Goldman
Journal:  J Cell Biol       Date:  1985-09       Impact factor: 10.539

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  18 in total

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Authors:  Kayla J Bayless; Greg A Johnson
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4.  Immunocytochemical demonstration of a new vimentin-associated protein in 3T3 fibroblasts.

Authors:  S M Wang; J S Chen; T H Fong; J C Wu
Journal:  Histochem J       Date:  1996-07

Review 5.  Intermediate filaments as dynamic structures.

Authors:  M W Klymkowsky
Journal:  Cancer Metastasis Rev       Date:  1996-12       Impact factor: 9.264

6.  Integrin alpha 6 beta 4 forms a complex with the cytoskeletal protein HD1 and induces its redistribution in transfected COS-7 cells.

Authors:  C M Niessen; E H Hulsman; E S Rots; P Sánchez-Aparicio; A Sonnenberg
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7.  M-phase-specific phosphorylation and structural rearrangement of the cytoplasmic cross-linking protein plectin involve p34cdc2 kinase.

Authors:  R Foisner; N Malecz; N Dressel; C Stadler; G Wiche
Journal:  Mol Biol Cell       Date:  1996-02       Impact factor: 4.138

8.  Pre-embedding Double-Label Immunoelectron Microscopy of Chemically Fixed Tissue Culture Cells.

Authors:  Lou G Boykins; Jonathan C R Jones; Carlos E Estraño; Steven D Schwartzbach; Omar Skalli
Journal:  Methods Mol Biol       Date:  2016

9.  Hemidesmosome formation is initiated by the beta4 integrin subunit, requires complex formation of beta4 and HD1/plectin, and involves a direct interaction between beta4 and the bullous pemphigoid antigen 180.

Authors:  R Q Schaapveld; L Borradori; D Geerts; M R van Leusden; I Kuikman; M G Nievers; C M Niessen; R D Steenbergen; P J Snijders; A Sonnenberg
Journal:  J Cell Biol       Date:  1998-07-13       Impact factor: 10.539

Review 10.  Plectin-intermediate filament partnership in skin, skeletal muscle, and peripheral nerve.

Authors:  Maria J Castañón; Gernot Walko; Lilli Winter; Gerhard Wiche
Journal:  Histochem Cell Biol       Date:  2013-06-09       Impact factor: 4.304

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