Literature DB >> 8505366

CD44 expression on murine tissues.

S J Kennel1, T K Lankford, L J Foote, S G Shinpock, C Stringer.   

Abstract

CD44 is a cell surface glycoprotein found on lymphoid and epithelial cells. Its primary function on lymphocytes and macrophages is to mediate interaction with endothelium, while its function on epithelial cells is not known. The protein has many different forms, generated by alternative mRNA splicing and by post-translational modification, which may mediate different functions. During previous work on murine lung tumor cells, mAb 133-13A was isolated and shown to recognize a surface glycoprotein, P100, of 90-100 x 10(3) M(r). Amino acid sequence analysis of purified P100 indicates that it is CD44. Since few data exist to indicate which forms of CD44 are present in different normal tissues, mAb 133-13A was used to analyze CD44 expression in mouse tissue. Quantitative data on the distribution of CD44(P100) in mice show that spleen, thymus, liver, intestine, uterus and choroid of the eye are major sites of expression. In addition, epithelia of adrenals, esophagus and trachea are CD44(P100) positive. Previous work on human cell lines has implicated a high molecular mass (130-160 x 10(3) M(r)) form of the glycoprotein as the form expressed in epithelial cells and carcinomas. Isolation of CD44 proteins from lymphoid tissues in the mouse indicate that, as in human lymphoid tissue, the low molecular mass form (80-90 x 10(3) M(r)) is predominately expressed. These data show that both small (approximately 81 x 10(3) M(r)) and large forms of the glycoprotein are expressed in basal epithelia of esophagus and trachea and in salivary gland, while only the small form is expressed in epithelium of the adrenal cortex and in the murine lung and mammary carcinomas studied. While these data cannot distinguish between specific splice variants, they show that the large forms of CD44 are minor components in normal tissue and seem to be found only in basal epithelium. The CD44 of low M(r) found in epithelial tissues is probably associated with lymphoid cell types in the tissues.

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Year:  1993        PMID: 8505366     DOI: 10.1242/jcs.104.2.373

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  30 in total

Review 1.  Forms and functions of CD44.

Authors:  G Borland; J A Ross; K Guy
Journal:  Immunology       Date:  1998-02       Impact factor: 7.397

2.  CD44 expression in normal adrenal tissue and adrenal tumours.

Authors:  I Barshack; I Goldberg; D Nass; D Olchovsky; J Kopolovic
Journal:  J Clin Pathol       Date:  1998-01       Impact factor: 3.411

3.  Impact of structurally modifying hyaluronic acid on CD44 interaction.

Authors:  D Bhattacharya; D Svechkarev; J J Souchek; T K Hill; M A Taylor; A Natarajan; A M Mohs
Journal:  J Mater Chem B       Date:  2017-09-20       Impact factor: 6.331

4.  Growth and differentiation regulate CD44 expression on human keratinocytes.

Authors:  J Zhou; J G Haggerty; L M Milstone
Journal:  In Vitro Cell Dev Biol Anim       Date:  1999-04       Impact factor: 2.416

5.  Radioimaging of light chain amyloid with a fibril-reactive monoclonal antibody.

Authors:  Jonathan S Wall; Stephen J Kennel; Mike Paulus; Jens Gregor; Tina Richey; James Avenell; Jeffrey Yap; David Townsend; Deborah T Weiss; Alan Solomon
Journal:  J Nucl Med       Date:  2006-12       Impact factor: 10.057

6.  Localization of CD44, the hyaluronate receptor, on the plasma membrane of osteocytes and osteoclasts in rat tibiae.

Authors:  H Nakamura; S Kenmotsu; H Sakai; H Ozawa
Journal:  Cell Tissue Res       Date:  1995-05       Impact factor: 5.249

Review 7.  CD44 in cancer progression: adhesion, migration and growth regulation.

Authors:  R Marhaba; M Zöller
Journal:  J Mol Histol       Date:  2004-03       Impact factor: 2.611

Review 8.  CD44: physiological expression of distinct isoforms as evidence for organ-specific metastasis formation.

Authors:  M Zöller
Journal:  J Mol Med (Berl)       Date:  1995-09       Impact factor: 4.599

9.  Select membrane proteins modulate MNV-1 infection of macrophages and dendritic cells in a cell type-specific manner.

Authors:  Juliana Bragazzi Cunha; Christiane E Wobus
Journal:  Virus Res       Date:  2016-06-02       Impact factor: 3.303

10.  In vivo biodistribution of siRNA and cisplatin administered using CD44-targeted hyaluronic acid nanoparticles.

Authors:  Shanthi Ganesh; Arun K Iyer; Florence Gattacceca; David V Morrissey; Mansoor M Amiji
Journal:  J Control Release       Date:  2013-10-22       Impact factor: 9.776

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