Background
The protein NKX2–5 affects mammalian heart development. In mice, the disruption of
Nkx2–5
has been associated with arrhythmias, abnormal myocardial contraction, abnormal cardiac morphogenesis, and death. However, the details of the mechanisms are unclear. This study was designed to investigate them.
Material/Methods
Rat cardiomyocytes from the H9c2 cell line were used in our study. First, we knocked down
Nkx2–5
in the H9c2 cells and then validated consequent changes in cell proliferation and migration. We then used RNA sequencing to determine the changes in transcripts. Finally, we validated these results by quantitative reverse transcription-polymerase chain reaction.
Results
We confirmed that
Nkx2–5
regulates the proliferation and migration of H9c2 cells. In our experiments,
Nkx2–5
regulated the expression of genes related to proliferation, migration, heart development, and disease. Based on bioinformatics analysis, knockdown of
Nkx2–5
caused differential expression of genes involved in cardiac development, calcium ion-related biological activity, the transforming growth factor (TGF)-β signaling pathway, pathways related to heart diseases, the MAPK signaling pathway, and other biological processes and signaling pathways.
Conclusions
Nkx2–5
may regulate proliferation and migration of the H9c2 cells through the genes
Tgfb-2
,
Bmp10
,
Id2
,
Wt1
,
Hey1
, and
Cacna1g
; rno-miR-1-3p; the TGF-β signaling pathway; the MAPK signaling pathway; as well as other genes and pathways.