Detection of muramyl dipeptide-sensing pathway defects in monocytes of patients with Crohn's disease using phospho-specific whole blood flow cytometry. (September 2013)

• Record Type: Journal Article
• Authors: Kuuliala, Krista; Lappalainen, Maarit; Turunen, Ulla; Puolakkainen, Pauli; Kemppainen, Esko; Siitonen, Sanna; Repo, Heikki; Mustonen, Harri
• Is Part Of: Scandinavian journal of clinical & laboratory investigation. Volume 73:Number 6(2013)
• Page Start: 494
• Page End: 502
• Publication Date: 2013-09
• Subjects: CARD15 mutations -- clinical screening -- leukocyte signaling; Clinical biochemistry -- Periodicals; Physiology, Pathological -- Periodicals; Physiology, Experimental -- Periodicals; Medicine -- Research -- Periodicals; Clinical medicine -- Periodicals; 616.0072
• DOI: 10.3109/00365513.2013.811612
• Languages: English
• ISSNs: 0036-5513

Abstract

Abstract: Peripheral blood mononuclear cells of Crohn's disease (CD) patients with the common 1007 fs mutation of the caspase recruitment domain-containing 15/nucleotide-binding oligomerization domain-containing 2 ( CARD15/NOD2 ) gene show impaired nuclear factor kappa B (NF-κB) activation in response to muramyl dipeptide (MDP), as determined by Western blotting. We applied phospho-specific flow cytometry to examine NF-κB and p38 activation in whole blood monocytes of 16 CD patients with or without the 1007 fs and previously described rare mutations of the CARD15 gene, and healthy reference subjects. Aliquots of whole blood were supplemented with MDP (0–1000 ng/mL), incubated for 10–40 min and processed for flow cytometry. Bacterial lipopolysaccharide (LPS) was used as a positive control agonist. We found that NF-κB and p38 phosphorylation induced by MDP was not detectable in monocytes of patients homozygous for the CARD15 1007 fs mutation, while those induced by LPS were normal. We also determined MDP-induced NF-κB phosphorylation levels in nuclear extracts of mononuclear cells separated from blood using enzyme-linked immunosorbent assay (ELISA), and observed that the levels decreased in a 1007 fs mutation-dose dependent manner. We conclude that phospho-specific whole blood flow cytometry provides a means to study phosphorylation of NF-κB and p38 in clinical samples and can be applied to screening of CD patients homozygous for the CARD15 1007 fs mutation.