Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/39450
Title: Generation of lentiviral-mediated shRNA vectors to inhibit the expression of caspase-1 and Pycard/ASC in dendritic cells.
Authors: Tan, Bee Kim.
Keywords: DRNTU::Science::Biological sciences::Microbiology::Immunology
Issue Date: 2010
Abstract: Dendritic cells (DC) originate from hematopoietic precursors and they detect endogenous and exogenous stimuli which lead to an inflammatory response. The “inflammasome” is a large protein complex which consists of Caspase-1 and Pycard/ASC which are involved in IL-1β and IL-18 processing. However, the role of DC in the recognition of these factors remains poorly understood. Recently, lentiviral vectors represented a tool to achieve a transient mode of gene-delivery to silence genes in hematopoetic cells. Here, we generated a third generation lentiviral vector system to deliver short-hairpin RNA (shRNA) to silence caspase-1 and Pycard/ASC in growth-factor-dependent murine DC (D1 cells). The generated shRNAs were successfully confirmed and cloned into lentiviral vectors for lentiviral transfection in HEK 293T cells. We observed that HeLa cells used for determining viral titers were not receptive to lentiviral transduction. On the contrary, transduced D1 cells demonstrated a high LNGFR+ expression profile ranging from 40% to 90% transduction efficiencies at 30 MOI. Collectively, we have generated an efficient lentiviral vector-mediated shRNA silencing system in primary cell lines which could provide an insight to into the biological mechanisms involved in inflammasome activation.
URI: http://hdl.handle.net/10356/39450
Rights: Nanyang Technological University
Fulltext Permission: restricted
Fulltext Availability: With Fulltext
Appears in Collections:SBS Student Reports (FYP/IA/PA/PI)

Files in This Item:
File Description SizeFormat 
SBS09-308.pdf
  Restricted Access
808.49 kBAdobe PDFView/Open

Google ScholarTM

Check

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.