[HTML][HTML] MicroRNA-15a-cell division cycle 42 signaling pathway in pathogenesis of pediatric inflammatory bowel disease
WJ Tang, KY Peng, ZF Tang, YH Wang… - World Journal of …, 2018 - ncbi.nlm.nih.gov
WJ Tang, KY Peng, ZF Tang, YH Wang, AJ Xue, Y Huang
World Journal of Gastroenterology, 2018•ncbi.nlm.nih.govAIM To determine whether cell division cycle (Cdc) 42 is regulated by microRNA (miR)-15a
in the development of pediatric inflammatory bowel disease (IBD). METHODS We cultured
293T cells, used plasmids and performed dual-luciferase assay to determine whether Cdc42
is a miR-15a target gene. We cultured Caco-2 cells, and stimulated them with tumor necrosis
factor (TNF)-α. We then employed lentiviruses to alter the expression of miR-15a and Cdc42.
We performed quantitative reverse transcription polymerase chain reaction (qRT-PCR) and …
in the development of pediatric inflammatory bowel disease (IBD). METHODS We cultured
293T cells, used plasmids and performed dual-luciferase assay to determine whether Cdc42
is a miR-15a target gene. We cultured Caco-2 cells, and stimulated them with tumor necrosis
factor (TNF)-α. We then employed lentiviruses to alter the expression of miR-15a and Cdc42.
We performed quantitative reverse transcription polymerase chain reaction (qRT-PCR) and …
Abstract
AIM
To determine whether cell division cycle (Cdc) 42 is regulated by microRNA (miR)-15a in the development of pediatric inflammatory bowel disease (IBD).
METHODS
We cultured 293T cells, used plasmids and performed dual-luciferase assay to determine whether Cdc42 is a miR-15a target gene. We cultured Caco-2 cells, and stimulated them with tumor necrosis factor (TNF)-α. We then employed lentiviruses to alter the expression of miR-15a and Cdc42. We performed quantitative reverse transcription polymerase chain reaction (qRT-PCR) and immunofluorescence to determine whether Cdc42 is regulated by miR-15a in Caco-2 cells. Finally, we collected ileocecal tissue by endoscopy from patients and performed qRT-PCR to examine the expression of miR-15a and Cdc42 in pediatric IBD patients.
RESULTS
Target Scan and dual-luciferase assay revealed that Cdc42 was a miR-15a target gene. MiR-15a expression increased (P= 0.0038) and Cdc42 expression decreased (P= 0.0013) in cells stimulated with TNF-α, and the expression of the epithelial junction proteins zona occludens (ZO)-1 (P< 0.05) and E-cadherin (P< 0.001) decreased. Cdc42 levels decreased in miR-15a-mimic cells (P< 0.001) and increased in miR-15a inhibitor cells (P< 0.05). ZO-1 and E-cadherin decreased in miR-15a-mimic cells (P< 0.001) but not in the miR-15a inhibitor+ TNF-α cells. In Lv-Cdc42+ TNF-α cells, ZO-1 and E-cadherin expression increased compared to the Lv-Cdc42-NC+ TNF-α (P< 0.05) or miR-15a-mimic cells (P< 0.05). Fifty-four pediatric IBD patients were included in this study, 21 in the control group, 19 in the Crohn’s disease (CD) active (AC) group, seven in the CD remission (RE) group, and seven in the ulcerative colitis (UC) group. MiR-15a increased and Cdc42 decreased in the CD AC group compared to the control group (P< 0.05). miR-15a decreased and Cdc42 increased in the CD RE group compared to the CD AC group (P< 0.05). miR-15a was positively correlated with the Pediatric Crohn’s disease Activity Index (PCDAI)(P= 0.006), while Cdc42 was negatively correlated with PCDAI (P= 0.0008). Finally, miR-15a expression negatively correlated with Cdc42 in pediatric IBD patients (P= 0.0045).
CONCLUSION
MiR-15a negatively regulates epithelial junctions through Cdc42 in Caco-2 cells and pediatric IBD patients.
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