Effects of pituitary adenylate cyclase activating polypeptide on small intestinal INT 407 cells. (October 2017)

• Record Type: Journal Article
• Authors: Illes, A.; Opper, B.; Reglodi, D.; Kerenyi, M.; Czetany, P.; Boronkai, A.; Schafer, E.; Toth, G.; Fabian, E.; Horvath, G.
• Is Part Of: Neuropeptides. Volume 65(2017)
• Page Start: 106
• Page End: 113
• Publication Date: 2017-10
• Subjects: INT 407 -- Cytoprotection -- Cell survival -- Irradiation -- Gene silencing; Neuropeptides -- Periodicals; Neuropeptides; Neuropeptides -- Périodiques; Neuropeptides; Electronic journals; Periodicals; 572.65
• DOI: 10.1016/j.npep.2017.07.002
• Languages: English
• ISSNs: 0143-4179

Abstract

Abstract: Pituitary adenylate cyclase activating polypeptide (PACAP) is an endogenous neuropeptide having a widespread distribution both in the nervous system and peripheral organs including the gastrointestinal tract. It has been shown to exert actions on intestinal functions, mainly affecting glandular secretion and motility. PACAP has several different effects on cell survival depending on the cell type and the applied stimulus. Its influences on small intestinal epithelial cells are not yet elucidated, therefore the aim of the present study was to investigate the effects of PACAP on intestinal epithelial cells having high turnover (INT 407) against different harmful stimuli, such as oxidative stress, in vitro hypoxia and gamma radiation. We tested the effect of PACAP on proliferation and cell survival using MTT assay. Moreover, various cancer-related factors were evaluated by oncology array. PACAP did not influence the proliferation rate of INT 407 cells. Its cell survival-enhancing effect could be detected against oxidative stress, but not against in vitro hypoxia or gamma irradiation. Clonogenic survival assay was performed to analyze the effect of PACAP on clonogenic potential of cells exposed to gamma radiation. Surprisingly, PACAP enhanced the clone-forming ability decrease induced by irradiation. Western blot analysis of ERK1/2 phosphorylation was performed in order to obtain further information on the molecular background. Our data showed phospho-ERK1/2 suppression of PACAP in irradiated cells. Furthermore, the role of endogenous PACAP against oxidative stress was also investigated performing ADCYAP1 small interfering RNA transfection. We found significant difference in the cell vulnerability between cells undergoing silencing and cells without transfection suggesting the protective role of the endogenously present PACAP against oxidative stress in INT 407 cells. In summary, PACAP seems to be able to exert contradictory effects in INT 407 cells depending on the applied stressor, suggesting its regulatory role in the cellular household. Highlights: Effects of PACAP in in small intestinal (INT 407) cells depend on the timing of treatment and applied stressor. PACAP alone does not influence proliferation of small intestinal epithelial cells. Both exogenous and endogenous PACAP is protective in H2 O2 -induced oxidative stress.