L-Glutamine Attenuates Apoptosis Induced by Endoplasmic Reticulum Stress by Activating the IRE1α-XBP1 Axis in IPEC-J2: A Novel Mechanism of L-Glutamine in Promoting Intestinal Health

Intestinal absorption and barrier malfunctions are associated with endoplasmic reticulum stress (ERS) in the intestine. We induced ERS by exposing the intestinal porcine epithelial cell line J2 (IPEC-J2) to tunicamycin (TUNI) to explore the potential of L-glutamine to reduce ERS-induced apoptosis. Our experiments demonstrated that exposing cells to TUNI results in spontaneous ERS and encourages the upregulation of glucose-regulated protein 78 (GRP78). Prolonged TUNI-induced ERS was found to increase apoptosis mediated by C/enhancer binding protein homologous protein (CHOP), accompanied by GRP78 downregulation. Treatment with L-glutamine was found to promote cell proliferation within the growth medium but to have little effect in basic Dulbecco's modified Eagle medium. Finally, in the milieu of TUNI-induced ERS, L-glutamine was found to maintain a high level of GRP78, alleviate CHOP-mediated apoptosis and activate the inositol requiring enzyme 1 alpha (IRE1 alpha)-X-box binding protein 1 (XBP1) axis. A specific inhibitor of the IRE1 alpha-XBP1 axis reversed the protective effect of L-glutamine by blocking the expression of IRE1 alpha/XBP1s. We propose that the functional effect of L-glutamine on intestinal health may be partly due to its modulation of ERS and CHOP-mediated apoptosis.