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Combinations of CD45 Isoforms Are Crucial for Immune Function and Disease
Author(s) -
Ritu Dawes,
Svetla Petrova,
Zhe Liu,
David C. Wraith,
Peter C. L. Beverley,
Elma Tchilian
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.176.6.3417
Subject(s) - gene isoform , biology , immune system , exon , transgene , haematopoiesis , t cell receptor , genetically modified mouse , autoimmune disease , experimental autoimmune encephalomyelitis , allele , immunology , microbiology and biotechnology , t cell , gene , genetics , antibody , stem cell
Expression of the CD45 Ag in hemopoietic cells is essential for normal development and function of lymphocytes, and both mice and humans lacking expression exhibit SCID. Human genetic variants of CD45, the exon 4 C77G and exon 6 A138G alleles, which alter the pattern of CD45 isoform expression, are associated with autoimmune and infectious diseases. We constructed transgenic mice expressing either an altered level or combination of CD45 isoforms. We show that the total level of CD45 expressed is crucial for normal TCR signaling, lymphocyte proliferation, and cytokine production. Most importantly, transgenic lines with a normal level, but altered combinations of CD45 isoforms, CD45(RABC/+) and CD45(RO/+) mice, which mimic variant CD45 expression in C77G and A138G humans, show more rapid onset and increased severity of experimental autoimmune encephalomyelitis. CD45(RO/+) cells produce more TNF-alpha and IFN-gamma. Thus, for the first time, we have shown experimentally that it is the combination of CD45 isoforms that affects immune function and disease.

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