TY - JOUR
T1 - Common gene expression patterns responsive to mild temperature hyperthermia in normal human fibroblastic cells
AU - Tabuchi, Yoshiaki
AU - Furusawa, Yukihiro
AU - Kariya, Ayako
AU - Wada, Shigehito
AU - Ohtsuka, Kenzo
AU - Kondo, Takashi
N1 - Funding Information:
Declaration of interest: This study was supported in part by a Grant-in-Aid from the Japanese Ministry of Education, Culture, Sports, Science and Technology. The authors alone are responsible for the content and writing of the paper.
PY - 2013
Y1 - 2013
N2 - Purpose: Heat stress induces complex cellular responses, and its detailed molecular mechanisms still remain to be clarified. The objective of this study was to investigate the molecular mechanisms underlying cellular responses to mild hyperthermia (MHT) in normal human fibroblastic (NHF) cells. Materials and methods: Cells were treated with MHT (41°C, 30min) and then cultured at 37°C. Gene expression was determined by the GeneChip® system and bioinformatics tools. Results: Treatment of the NHF cell lines, Hs68 and OUMS-36, with MHT did not affect the cell viability or cell cycle. In contrast, many probe sets were differentially expressed by >1.5-fold in both cell lines after MHT treatment. Of the 1,196 commonly and differentially expressed probe sets analysed by k-means clustering, three gene clusters, Up-I, Down-I and Down-II, were observed. Interestingly, two gene networks were obtained from the up-regulated genes in cluster Up-I. The gene network E contained DDIT3 and HSPA5 and was mainly associated with the biological process of endoplasmic reticulum stress, while the network S contained HBEGF and LIF and was associated with the biological process of cell survival. Eighteen genes were validated by quantitative real-time polymerase chain reaction, consistent with the microarray data, in four kinds of NHF cells. Conclusions: Common genes that were differentially expressed and/or acted within a gene network in response to MHT in NHF cells were identified. These findings provide the molecular basis for a further understanding of the mechanisms of the MHT response in NHF cells.
AB - Purpose: Heat stress induces complex cellular responses, and its detailed molecular mechanisms still remain to be clarified. The objective of this study was to investigate the molecular mechanisms underlying cellular responses to mild hyperthermia (MHT) in normal human fibroblastic (NHF) cells. Materials and methods: Cells were treated with MHT (41°C, 30min) and then cultured at 37°C. Gene expression was determined by the GeneChip® system and bioinformatics tools. Results: Treatment of the NHF cell lines, Hs68 and OUMS-36, with MHT did not affect the cell viability or cell cycle. In contrast, many probe sets were differentially expressed by >1.5-fold in both cell lines after MHT treatment. Of the 1,196 commonly and differentially expressed probe sets analysed by k-means clustering, three gene clusters, Up-I, Down-I and Down-II, were observed. Interestingly, two gene networks were obtained from the up-regulated genes in cluster Up-I. The gene network E contained DDIT3 and HSPA5 and was mainly associated with the biological process of endoplasmic reticulum stress, while the network S contained HBEGF and LIF and was associated with the biological process of cell survival. Eighteen genes were validated by quantitative real-time polymerase chain reaction, consistent with the microarray data, in four kinds of NHF cells. Conclusions: Common genes that were differentially expressed and/or acted within a gene network in response to MHT in NHF cells were identified. These findings provide the molecular basis for a further understanding of the mechanisms of the MHT response in NHF cells.
KW - Mild temperature hyperthermia
KW - gene function
KW - gene network
KW - microarray
KW - normal human fibroblastic cell
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U2 - 10.3109/02656736.2012.753163
DO - 10.3109/02656736.2012.753163
M3 - Article
C2 - 23311377
AN - SCOPUS:84872298409
SN - 0265-6736
VL - 29
SP - 38
EP - 50
JO - International Journal of Hyperthermia
JF - International Journal of Hyperthermia
IS - 1
ER -