| Literature DB >> 27162272 |
F Matthew Kuhlmann1, Srikanth Santhanam2, Pardeep Kumar1, Qingwei Luo1, Matthew A Ciorba3, James M Fleckenstein4.
Abstract
Because O blood group has been associated with more severe cholera infections, it has been hypothesized that cholera toxin (CT) may bind non-O blood group antigens of the intestinal mucosae, thereby preventing efficient interaction with target GM1 gangliosides required for uptake of the toxin and activation of cyclic adenosine monophosphate (cAMP) signaling in target epithelia. Herein, we show that after exposure to CT, human enteroids expressing O blood group exhibited marked increase in cAMP relative to cells derived from blood group A individuals. Likewise, using CRISPR/Cas9 engineering, a functional group O line (HT-29-A(-/-)) was generated from a parent group A HT-29 line. CT stimulated robust cAMP responses in HT-29-A(-/-) cells relative to HT-29 cells. These findings provide a direct molecular link between blood group O expression and differential cellular responses to CT, recapitulating clinical and epidemiologic observations. © The American Society of Tropical Medicine and Hygiene.Entities:
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Year: 2016 PMID: 27162272 PMCID: PMC4973196 DOI: 10.4269/ajtmh.16-0161
Source DB: PubMed Journal: Am J Trop Med Hyg ISSN: 0002-9637 Impact factor: 2.345