
Supplementary choline attenuates olive oil lipid emulsion‐induced enterocyte apoptosis through suppression of CELF 1/ AIF pathway
Author(s) -
Yan JunKai,
Zhu Jie,
Gong ZiZhen,
Wen Jie,
Xiao YongTao,
Zhang Tian,
Cai Wei
Publication year - 2018
Publication title -
journal of cellular and molecular medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.44
H-Index - 130
eISSN - 1582-4934
pISSN - 1582-1838
DOI - 10.1111/jcmm.13430
Subject(s) - enterocyte , apoptosis , choline , apoptosis inducing factor , microbiology and biotechnology , biology , chemistry , biochemistry , caspase , programmed cell death , small intestine
Enterocyte apoptosis induced by lipid emulsions is a key cause of intestinal atrophy under total parenteral nutrition ( TPN ) support, and our previous work demonstrated that olive oil lipid emulsion ( OOLE ) could induce enterocyte apoptosis via CUGBP , Elav‐like family member 1 ( CELF 1)/ apoptosis‐inducing factor ( AIF ) pathway. As TPN ‐associated complications are partially related to choline deficiency, we aimed to address whether choline supplementation could attenuate OOLE ‐induced enterocyte apoptosis. Herein we present evidence that supplementary choline exhibits protective effect against OOLE ‐induced enterocyte apoptosis both in vivo and in vitro . In a rat model of TPN , substantial reduction in apoptotic rate along with decreased expression of CELF 1 was observed when supplementary choline was added to OOLE . In cultured Caco‐2 cells, supplementary choline attenuated OOLE ‐induced apoptosis and mitochondria dysfunction by suppressing CELF 1/ AIF pathway. Compared to OOLE alone, the expression of CELF 1 and AIF was significantly decreased by supplementary choline, whereas the expression of Bcl‐2 was evidently increased. No obvious alterations were observed in Bax expression and caspase‐3 activation. Mechanistically, supplementary choline repressed the expression of CELF 1 by increasing the recruitment of CELF 1 mRNA to processing bodies, thus resulting in suppression of its protein translation. Taken together, our data suggest that supplementary choline exhibits effective protection against OOLE ‐induced enterocyte apoptosis, and thus, it has the potential to be used for the prevention and treatment of TPN ‐induced intestinal atrophy.