HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Cross-species analysis of nicotine-induced proteomic alterations in pancreatic cells.

Abstract
Toxic compounds in tobacco, such as nicotine, may adversely affect pancreatic function. We aim to determine nicotine-induced protein alterations in pancreatic cells, thereby revealing links between nicotine exposure and pancreatic disease. We compared the proteomic alterations induced by nicotine treatment in cultured pancreatic cells (mouse, rat, and human stellate cells and human duct cells) using MS-based techniques, specifically SDS-PAGE (gel) coupled with LC-MS/MS and spectral counting. We identified thousands of proteins in pancreatic cells, hundreds of which were identified exclusively or in higher abundance in either nicotine-treated or untreated cells. Interspecies comparisons of stellate cell proteins revealed several differentially abundant proteins (in nicotine treated versus untreated cells) common among the three species. Proteins appearing in all nicotine-treated stellate cells include amyloid beta (A4), procollagen type VI alpha 1, integral membrane protein 2B, and toll-interacting protein. Proteins that were differentially expressed upon nicotine treatment across cell lines were enriched in certain pathways, including nicotinic acetylcholine receptor, cytokine, and integrin signaling. At this analytical depth, we conclude that similar pathways are affected by nicotine, but alterations at the protein level among stellate cells of different species vary. Further interrogation of such pathways will lead to insights into the potential effect of nicotine on pancreatic cells at the biomolecular level and the extension of this concept to the effect of nicotine on pancreatic disease.
AuthorsJoao A Paulo, Raul Urrutia, Vivek Kadiyala, Peter Banks, Darwin L Conwell, Hanno Steen
JournalProteomics (Proteomics) Vol. 13 Issue 9 Pg. 1499-1512 (May 2013) ISSN: 1615-9861 [Electronic] Germany
PMID23456891 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Chemical References
  • Adaptor Proteins, Signal Transducing
  • Amyloid beta-Peptides
  • Collagen Type VI
  • ITM2B protein, human
  • Membrane Glycoproteins
  • Proteins
  • Nicotine
Topics
  • Adaptor Proteins, Signal Transducing
  • Amyloid beta-Peptides (metabolism)
  • Animals
  • Cell Line
  • Cells, Cultured
  • Collagen Type VI (metabolism)
  • Electrophoresis, Polyacrylamide Gel
  • Humans
  • Membrane Glycoproteins (metabolism)
  • Mice
  • Nicotine (pharmacology)
  • Pancreas (cytology, drug effects, metabolism)
  • Pancreatic Stellate Cells (drug effects, metabolism)
  • Proteins (analysis, metabolism)
  • Rats
  • Signal Transduction (drug effects)
  • Species Specificity
  • Tandem Mass Spectrometry (methods)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: