| Literature DB >> 26345430 |
Catherine Bonnefont-Rebeix1, Corinne Fournel-Fleury2, Frédérique Ponce2, Sara Belluco2, Dorothée Watrelot2, Sylvie E Bouteille2, Sylvie Rapiteau2, Diane Razanajaona-Doll3, Jean-Jacques Pin3, Caroline Leroux4, Thierry Marchal2.
Abstract
Dogs with lymphoma are established as good model for human non-Hodgkin lymphoma studies. Canine cell lines derived from lymphomas may be valuable tools for testing new therapeutic drugs. In this context, we established a canine T-cell line, PER-VAS, from a primary aggressive T-cell lymphoma with large granular morphology. Flow cytometric analysis revealed a stable immunophenotype: PER-VAS cells were positively labelled for CD5, CD45, MHC II and TLR3, and were negative for CD3, CD4 and CD8 expression. Although unstable along the culture process, IL-17 and MMP12 proteins were detectable as late as at passages 280 and 325i.e. respectively 24 and 29 months post isolation. At passage 325, PER-VAS cells maintained the expression of IL-17, CD3, CD56, IFNγ and TNFα mRNAs as shown by RT-PCR analysis. Stable rearrangement of the TCRγ gene has been evidenced by PCR. PER-VAS cells have a high proliferation index with a doubling time of 16.5h and were tumorigenic in Nude mice. Compared to the canine cell lines already reported, PER-VAS cells display an original expression pattern, close to NKT cells, which makes them valuable tools for in vitro comparative research on lymphomas.Entities:
Keywords: CD56 mRNA; Cell line; Dog; IL-17; T-cell lymphoma
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Year: 2015 PMID: 26345430 DOI: 10.1016/j.imbio.2015.08.007
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144