scholarly journals Induction of CD44 Variant Isoforms is an Early Epithelial Response to Helicobacter pylori Infection

2019 ◽  
Vol 33 (S1) ◽  
Author(s):  
Jayati Chakrabarti ◽  
Nina Steele ◽  
Loryn Holokai ◽  
Taylor Broda ◽  
Jacek Biesiada ◽  
...  
1994 ◽  
Vol 124 (1) ◽  
pp. 71-82 ◽  
Author(s):  
CR Mackay ◽  
HJ Terpe ◽  
R Stauder ◽  
WL Marston ◽  
H Stark ◽  
...  

CD44 is a ubiquitous surface molecule that exists as a number of isoforms, generated by alternative splicing of 10 "variant" exons. Little is known about the expression and function of the variant isoforms, except that certain isoforms may play a role in cancer metastasis. We produced mAbs against CD44 variant regions encoded by exons 4v, 6v, and 9v, by immunizing mice with a fusion protein spanning variant exons 3v to 10v. A comprehensive analysis of human tissues revealed that CD44 variant isoforms were expressed widely throughout the body, principally by epithelial cells. However there was differential expression of CD44 variant exons by different epithelia. Most epithelia expressed exon 9v, but much fewer expressed 6v or 4v. The regions of epithelia that expressed the highest levels of the variant isoforms were the generative cells, particularly the basal cells of stratified squamous epithelium, and of glandular epithelium. CD44 variant isoforms were also expressed differentially by leukocytes, with CD44-9v expressed at very low levels and CD44-6v and 4v virtually absent. However, CD44-9v and CD44-6v were the main variants that were transiently upregulated on T cells after mitogenic stimulation and on myelomonocytic cell lines by TNF alpha and IFN gamma treatment. Some epithelial cell lines could preferentially upregulate CD44-6v upon IFN gamma incubation. These results show that CD44 variant isoforms are expressed much more widely than first appreciated, and that expression of the variant isoforms on some cell types can be modulated by particular cytokines.


2013 ◽  
Vol 27 (9) ◽  
pp. 3683-3701 ◽  
Author(s):  
Lizette Ghazi‐Visser ◽  
Jon D. Laman ◽  
Sabine Nagel ◽  
Marjan Meurs ◽  
Debby Riel ◽  
...  

1997 ◽  
Vol 57 (1-3) ◽  
pp. 217-223 ◽  
Author(s):  
B Wittig ◽  
S Seiter ◽  
N Föger ◽  
C Schwärzler ◽  
U Günthert ◽  
...  

1998 ◽  
Vol 16 ◽  
pp. S4
Author(s):  
Simone Seiter ◽  
Marc Rösel ◽  
Uulla Günthert ◽  
Wolfgang Tilgen ◽  
Margot Zöller

Blood ◽  
1995 ◽  
Vol 85 (10) ◽  
pp. 2885-2899 ◽  
Author(s):  
R Stauder ◽  
W Eisterer ◽  
J Thaler ◽  
U Gunthert

Isoforms of the transmembrane glycoprotein CD44, generated by alternative RNA splicing, have been correlated to tumor dissemination. For evaluation of the potential role of CD44 variant isoforms in non- Hodgkin's lymphoma (NHL), the presence of CD44 isoforms was analyzed in a large panel of reactive and neoplastic lymphoid tissues by immunohistochemical staining, as well as detection of CD44 variant RNAs by the reverse transcriptase-polymerase chain reaction. Whereas the CD44 standard or hematopoietic isoform (CD44s), devoid of the variant regions, was expressed in all leukocyte subpopulations, the variant isoforms (CD44v) showed a highly restricted pattern of expression, mainly observed in epithelial layers of lymphoid tissues and subpopulations of leukocytes after stimulation. In addition to a strong expression of CD44s, variant isoforms containing CD44–6v in combination with other variant exons were observed predominantly in aggressive lymphoma and were associated with a shorter overall survival of patients (n = 138; P < .0001). Moreover, multivariate analysis indicated CD44–6v as a new independent prognostic parameter in high grade NHL in comparison with the risk groups defined by the International NHL Lymphoma Prognostic Factors Project (N Engl J Med 329:987, 1993).


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