TY - JOUR
T1 - Activated Mast Cells in Proximity to Colonic Nerves Correlate with Abdominal Pain in Irritable Bowel Syndrome
AU - Barbara, Giovanni
AU - Stanghellini, Vincenzo
AU - De Giorgio, Roberto
AU - Cremon, Cesare
AU - Cottrell, Graeme S.
AU - Santini, Donatella
AU - Pasquinelli, Gianandrea
AU - Morselli-Labate, Antonio M.
AU - Grady, Eileen F.
AU - Bunnett, Nigel W.
AU - Collins, Stephen M.
AU - Corinaldesi, Roberto
N1 - Funding Information:
The authors are grateful to all investigators and contributing pathologists from the TCGA study (more information on http://portal.gdc.cancer.gov ), the Rainbow-TMA consortium in the Netherlands (listed in Supplementary Table 6 ), the DACHS consortium in Germany, the QUASAR consortium, and the YCR-BCIP consortium in the United Kingdom. Collection and testing of the YCR-BCIP cases was funded by Yorkshire Cancer Research L386 and L394 as part of previous studies. Philip Quirke is an NIHR Senior Investigator. We thank the Yorkshire and Humber Histopathologists who facilitated the collection of the YCR BCIP cases.
Funding Information:
Funding This study was primarily funded by the authors’ academic institutions. These authors are supported by additional grants: Peter Boor: German Research Foundation (SFB/TRR57, SFB/TRR219, BO3755/3-1, and BO3755/6-1), the German Federal Ministry of Education and Research (BMBF: STOP-FSGS-01GM1901A), and the German Federal Ministry of Economic Affairs and Energy (BMWi: EMPAIA project). Alexander T. Pearson: National Institutes of Health / National Institute of Dental and Craniofacial Research (K08-DE026500), Institutional Research Grant (IRG-16-222-56) from the American Cancer Society , Cancer Research Foundation Research Grant, and the University of Chicago Medicine Comprehensive Cancer Center Support Grant (P30-CA14599). Tom Luedde: Horizon 2020 through the European Research Council Consolidator Grant PhaseControl (771083), a Mildred Scheel–Endowed Professorship from the German Cancer Aid (Deutsche Krebshilfe), the German Research Foundation (SFB CRC1382/P01, SFB-TRR57/P06, LU 1360/3-1), the Ernst-Jung-Foundation Hamburg , and the Interdisciplinary Center of Clinical Research) at RWTH Aachen. Jakob Nikolas Kather: RWTH University Aachen (START 2018-691906), Max-Eder-Programme of the German Cancer Aid (Deutsche Krebshilfe, 70113864).
PY - 2004/3
Y1 - 2004/3
N2 - Background & Aims: The mechanisms underlying abdominal pain perception in irritable bowel syndrome (IBS) are poorly understood. Intestinal mast cell infiltration may perturb nerve function leading to symptom perception. We assessed colonic mast cell infiltration, mediator release, and spatial interactions with mucosal innervation and their correlation with abdominal pain in IBS patients. Methods: IBS patients were diagnosed according to Rome II criteria and abdominal pain quantified according to a validated questionnaire. Colonic mucosal mast cells were identified immunohistochemically and quantified with a computer-assisted counting method. Mast cell tryptase and histamine release were analyzed immunoenzymatically. Intestinal nerve to mast cell distance was assessed with electron microscopy. Results: Thirty-four out of 44 IBS patients (77%) showed an increased area of mucosa occupied by mast cells as compared with controls (9.2% ± 2.5% vs. 3.3 ± 0.8%, respectively; P < 0.001). There was a 150% increase in the number of degranulating mast cells (4.76 ± 3.18/field vs. 2.42 ± 2.26/field, respectively; P = 0.026). Mucosal content of tryptase was increased in IBS and mast cells spontaneously released more tryptase (3.22 ± 3.48 pmol/min/mg vs. 0.87 ± 0.65 pmol/min/mg, respectively; P = 0.015) and histamine (339.7 ± 59.0 ng/g vs. 169.3 ± 30.6 ng/g, respectively; P = 0.015). Mast cells located within 5 μm of nerve fibers were 7.14 ± 3.87/field vs. 2.27 ± 1.63/field in IBS vs. controls (P < 0.001). Only mast cells in close proximity to nerves were significantly correlated with severity and frequency of abdominal pain/discomfort (P < 0.001 and P = 0.003, respectively). Conclusions: Colonic mast cell infiltration and mediator release in proximity to mucosal innervation may contribute to abdominal pain perception in IBS patients.
AB - Background & Aims: The mechanisms underlying abdominal pain perception in irritable bowel syndrome (IBS) are poorly understood. Intestinal mast cell infiltration may perturb nerve function leading to symptom perception. We assessed colonic mast cell infiltration, mediator release, and spatial interactions with mucosal innervation and their correlation with abdominal pain in IBS patients. Methods: IBS patients were diagnosed according to Rome II criteria and abdominal pain quantified according to a validated questionnaire. Colonic mucosal mast cells were identified immunohistochemically and quantified with a computer-assisted counting method. Mast cell tryptase and histamine release were analyzed immunoenzymatically. Intestinal nerve to mast cell distance was assessed with electron microscopy. Results: Thirty-four out of 44 IBS patients (77%) showed an increased area of mucosa occupied by mast cells as compared with controls (9.2% ± 2.5% vs. 3.3 ± 0.8%, respectively; P < 0.001). There was a 150% increase in the number of degranulating mast cells (4.76 ± 3.18/field vs. 2.42 ± 2.26/field, respectively; P = 0.026). Mucosal content of tryptase was increased in IBS and mast cells spontaneously released more tryptase (3.22 ± 3.48 pmol/min/mg vs. 0.87 ± 0.65 pmol/min/mg, respectively; P = 0.015) and histamine (339.7 ± 59.0 ng/g vs. 169.3 ± 30.6 ng/g, respectively; P = 0.015). Mast cells located within 5 μm of nerve fibers were 7.14 ± 3.87/field vs. 2.27 ± 1.63/field in IBS vs. controls (P < 0.001). Only mast cells in close proximity to nerves were significantly correlated with severity and frequency of abdominal pain/discomfort (P < 0.001 and P = 0.003, respectively). Conclusions: Colonic mast cell infiltration and mediator release in proximity to mucosal innervation may contribute to abdominal pain perception in IBS patients.
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U2 - 10.1053/j.gastro.2003.11.055
DO - 10.1053/j.gastro.2003.11.055
M3 - Article
C2 - 14988823
AN - SCOPUS:10744225624
SN - 0016-5085
VL - 126
SP - 693
EP - 702
JO - Gastroenterology
JF - Gastroenterology
IS - 3
ER -