Literature DB >> 3519624

Mechanisms of cytoskeletal regulation: modulation of aortic endothelial cell protein band 4.1 by the extracellular matrix.

T L Leto, B M Pratt, J A Madri.   

Abstract

The bovine aortic endothelial cell (BAEC) cytoskeleton is a complex structure modulated by many stimuli including release from contact inhibition and various components of the extracellular matrix (ECM). Transduction of information from the ECM to the cell nucleus proceeds via several complex pathways including the cytoskeleton. We have demonstrated the presence of an immunoreactive isoform of the human erythrocyte cytoskeletal protein band 4.1 (4.1) in BAEC. BAEC 4.1 is similar in molecular weight to the erythroid protein by immunoblot analyses and produces a similar pattern of cysteine specific cleavage products consistent with a cluster of cysteine residues previously described in the erythroid molecule. We have also examined the effects of defined ECM proteins on the distributions of cultured BAEC 4.1 and actin filaments (AF) at confluency and following release from contact inhibition. The distribution of 4.1 in BAEC on a plasma fibronectin substrate is complex, having partial codistribution with cytoplasmic AF and a unique perinuclear staining. In contrast, on a collagen type I/III substrate, 4.1 is localized, in part, to peripheral areas of cell-cell contact distinct from the dense peripheral band staining of AF. During migration on this substrate, 4.1 had a filamentous distribution having partial codistribution with AF. Indirect immunofluorescence staining of cross-sections of bovine calf aortae revealed a cortical staining pattern in the aortic endothelial cells with staining noted on the luminal and basolateral aspects of the cells. These data suggest that, in endothelial cells, protein 4.1 is a cortical membrane protein which may function to link actin filaments to other skeletal proteins such as spectrin. These findings also suggest an active role for protein 4.1 in cytoskeletal reorganization events which can occur in response to external stimuli, such as the extracellular matrix or contact with other cells.

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Year:  1986        PMID: 3519624     DOI: 10.1002/jcp.1041270311

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  26 in total

1.  The N-terminal 209-aa domain of high molecular-weight 4.1R isoforms abrogates 4.1R targeting to the nucleus.

Authors:  C M Luque; M J Lallena; C M Pérez-Ferreiro; Y de Isidro; G De Cárcer; M A Alonso; I Correas
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

2.  A nonerythroid isoform of protein 4.1R interacts with components of the contractile apparatus in skeletal myofibers.

Authors:  A Kontrogianni-Konstantopoulos; S C Huang; E J Benz
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

3.  Inhibition of protein 4.1 R and NuMA interaction by mutagenization of their binding-sites abrogates nuclear localization of 4.1 R.

Authors:  Subhendra N Mattagajasingh; Shu-Ching Huang; Edward J Benz
Journal:  Clin Transl Sci       Date:  2009-04       Impact factor: 4.689

4.  Protein 4.1R self-association: identification of the binding domain.

Authors:  Carmen M Pérez-Ferreiro; Eva Lospitao; Isabel Correas
Journal:  Biochem J       Date:  2006-12-15       Impact factor: 3.857

5.  Structural protein 4.1 is located in mammalian centrosomes.

Authors:  S W Krauss; J A Chasis; C Rogers; N Mohandas; G Krockmalnic; S Penman
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

6.  Identification, cloning, and expression of a cytosolic megakaryocyte protein-tyrosine-phosphatase with sequence homology to cytoskeletal protein 4.1.

Authors:  M X Gu; J D York; I Warshawsky; P W Majerus
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-01       Impact factor: 11.205

7.  Modulation of cell spreading and migration by pp125FAK phosphorylation.

Authors:  S Sankar; N Mahooti-Brooks; G Hu; J A Madri
Journal:  Am J Pathol       Date:  1995-09       Impact factor: 4.307

Review 8.  Communication between the cell membrane and the nucleus: role of protein compartmentalization.

Authors:  S A Lelièvre; M J Bissell
Journal:  J Cell Biochem Suppl       Date:  1998

Review 9.  Role of tissue specific alternative pre-mRNA splicing in the differentiation of the erythrocyte membrane.

Authors:  E J Benz; S C Huang
Journal:  Trans Am Clin Climatol Assoc       Date:  1997

10.  Characterization of isoforms of protein 4.1 present in the nucleus.

Authors:  I Correas
Journal:  Biochem J       Date:  1991-10-15       Impact factor: 3.857

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