TY - JOUR
T1 - Ultrasound stimulation induces microRNA expression changes that could be involved in sonication-induced apoptosis
AU - Ogawa, Ryohei
AU - Morii, Akihiro
AU - Watanabe, Akihiko
N1 - Funding Information:
Acknowledgments This research was supported by the Research and Development Committee Program of The Japan Society of Ultrasonics in Medicine. The authors thank Drs. Loreto B. Feril, Jr., and Go Kagiya for their critical reading of the manuscript.
PY - 2012/10
Y1 - 2012/10
N2 - Purpose The purpose of this study is to investigate the involvement of microRNAs (miRNAs) in sonicationinduced apoptosis. Methods U937 cells derived from human leukemia were sonicated with 1-MHz ultrasound at 0.4 W/cm2 and 10 % duty factor for 60 s, a condition inducing apoptosis. The total RNA was extracted from cells at various timings after sonication and subjected to microarray and real-time PCR for miRNA expression analyses. Results Expression of several miRNAs was significantly affected by sonication. For miR-424 and miR-720, whose expressions were eminently decreased by sonication, cell lines overexpressing these miRNAs were established. Conversely, for miR-663B and miR-663, whose expressions were eminently increased by sonication, cell lines inhibiting these miRNA functions were established. When these cell lines were sonicated, a cell line inhibiting miR- 663B function significantly increased sonication-induced apoptosis, suggesting this may be involved in cellular responses to sonication. Two genes that could induce apoptosis, KSR2 and CREBZF, were identified as potential target genes of miR-663B since potential target sequences on their 30 UTR mediated to decrease expression of a reporter gene. Conclusion These results suggest that miRNAs may be involved in cellular responses to ultrasound through their expression changes caused by sonication.
AB - Purpose The purpose of this study is to investigate the involvement of microRNAs (miRNAs) in sonicationinduced apoptosis. Methods U937 cells derived from human leukemia were sonicated with 1-MHz ultrasound at 0.4 W/cm2 and 10 % duty factor for 60 s, a condition inducing apoptosis. The total RNA was extracted from cells at various timings after sonication and subjected to microarray and real-time PCR for miRNA expression analyses. Results Expression of several miRNAs was significantly affected by sonication. For miR-424 and miR-720, whose expressions were eminently decreased by sonication, cell lines overexpressing these miRNAs were established. Conversely, for miR-663B and miR-663, whose expressions were eminently increased by sonication, cell lines inhibiting these miRNA functions were established. When these cell lines were sonicated, a cell line inhibiting miR- 663B function significantly increased sonication-induced apoptosis, suggesting this may be involved in cellular responses to sonication. Two genes that could induce apoptosis, KSR2 and CREBZF, were identified as potential target genes of miR-663B since potential target sequences on their 30 UTR mediated to decrease expression of a reporter gene. Conclusion These results suggest that miRNAs may be involved in cellular responses to ultrasound through their expression changes caused by sonication.
KW - Apoptosis
KW - Expression
KW - MicroRNA
KW - Microarray
UR - http://www.scopus.com/inward/record.url?scp=84868382701&partnerID=8YFLogxK
U2 - 10.1007/s10396-012-0364-9
DO - 10.1007/s10396-012-0364-9
M3 - 学術論文
C2 - 27279106
AN - SCOPUS:84868382701
SN - 1346-4523
VL - 39
SP - 207
EP - 216
JO - Journal of Medical Ultrasonics
JF - Journal of Medical Ultrasonics
IS - 4
ER -