Abnormal Activation of Autophagy-Induced Crinophagy in Paneth Cells From Patients With Crohn's Disease
Autophagy-related 16 like-1 (ATG16L-1), immunity-related GTPase-M (IRGM), and nucleotide-binding oligomerization domain-containing 2 (NOD2) regulate autophagy, and variants in these genes have been associated with predisposition to Crohn's disease (CD). However, little is known about the role of autophagy in CD. Intestinal biopsies from untreated pediatric patients with CD, celiac disease, or ulcerative colitis were analyzed by immunohistochemistry and electron microscopy. We observed that autophagy was specifically activated in Paneth cells from patients with CD, independently of mucosal inflammation or disease-associated variants of ATG16L1 or IRGM. In these cells, activation of autophagy was associated with a significant decrease in number of secretory granules and features of crinophagy. These observations might account for the disorganization of secretory granules previously reported in Paneth cells from patients with CD.
Keywords: Secretion , Lysosome , Organelle
Abbreviations used in this paper: ATG16L1, autophagy-related 16 like-1, CD, Crohn's disease, IRGM, immunity-related GTPase-M, LC3, microtubule-associated protein 1 light chain 3, NOD2, nucleotide-binding oligomerization domain-containing 2.
To access this article, please choose from the options below
Conflicts of interest The authors disclose no conflicts.
Funding This work was supported by Association François Aupetit (AFA), Institut National de la Santé et de la Recherche Médicale (INSERM), Assistance Publique-Hôpitaux de Paris (AP-HP), University Denis Diderot, Sorbonne Paris-Cité.
PII: S0016-5085(12)00151-5
doi:10.1053/j.gastro.2012.01.031
© 2012 AGA Institute. Published by Elsevier Inc. All rights reserved.

