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Apoptosis induced by a purified fraction (VB-P4) of the fresh water snail viviparous bengalensis flesh extract on osteoarthritic fibroblast like synoviocyte cells
Published in Bentham Science Publishers B.V.
Volume: 13
Issue: 7
Pages: 638 - 645
Objective: To evaluate apoptotic activity of Viviparous bengalensis flesh extracted purified fraction VB-P4 on fibroblast like synoviocyte cells (FLS). Methods: Purified fraction VB-P4 was analyzed for apoptotic activity on synoviocyte cell. The cells were treated with VB-P4 (40 μg/mL) for 24 hrs. Morphological analysis through phase contrast microscope, MTT assay for cytotoxicity study, interleukins level analysis, CD3, CD4, CD8 activities study through flow cytometry, apoptotic activity study using annexin V-FITC, immunofluorescence study of caspase 3, and agarose gel for DNA breakage were done using synoviocyte cell. Results: VB-P4 treatment on synovial cell showed lack of matured synoviocyte cell with respect to osteoarthritic control cells. MTT assay showed significant decrease in formazan complex formation after treatment with VB-P4 in dose dependent manner. Decreased levels of interleukins (TNF-α, IL-1β, CINC-1, IL-17, MMP-1, Cathepsin K) on synoviocyte cells also confirmed reduced osteoarthritis after treatment with VB-P4 (40 μg/mL). Flow cytometric analysis of monoclonal antibody (CD3, CD4, and CD8) exhibited increased expression on synovial cell surface after treatment with VBP4. Annexin-V FITC study showed 76.90%early apoptosis and 7.95%late apoptotic cell after treatment with VB-P4 which confirmed apoptotic activity of VB-P4 on osteoarthritic synoviocyte cells. Agarose gel electrophoresis showed that VB-P4 (40 μg/mL) worked on nuclear localization of synoviocyte which is shown by smeary bands and florescence cell micrograph. Upregulation of caspase 3 confirmed apoptosis due to VB-P4 treatment on synoviocyte cell. Conclusion: The findings showed that fresh water snail flesh extracted purified fraction VB-P4, exhibited apoptotic activity on osteoarthritic synoviocyte cell through caspase mediated pathway.
About the journal
JournalLetters in Drug Design and Discovery
PublisherBentham Science Publishers B.V.