TY - JOUR
T1 - Profiling molecular changes induced by hydrogen treatment of lung allografts prior to procurement
AU - Tanaka, Yugo
AU - Shigemura, Norihisa
AU - Kawamura, Tomohiro
AU - Noda, Kentaro
AU - Isse, Kumiko
AU - Stolz, Donna Beer
AU - Billiar, Timothy R.
AU - Toyoda, Yoshiya
AU - Bermudez, Christian A.
AU - Lyons-Weiler, James
AU - Nakao, Atsunori
N1 - Funding Information:
The Illumina gene expression data used in this study were generated by the University of Pittsburgh Genomics and Proteomics Core Laboratory. This publication was made possible in part by Grant No. 5 UL1 RR024153 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH), and NIH Roadmap for Medical Research, R21 HL102528-01, and the research funds of the Department of Cardiothoracic Surgery. Its contents are solely the responsibility of the authors and do not necessarily represent the official view of NCRR or NIH. Information on the NCRR is available at http://www.ncrr.nih.gov/ . Information on Re-engineering the Clinical Research Enterprise can be obtained from http://nihroadmap.nih.gov/clinicalresearch/overview-translational.asp .
PY - 2012/9/7
Y1 - 2012/9/7
N2 - Background: We previously demonstrated that donor treatment with inhaled hydrogen protects lung grafts from cold ischemia/reperfusion (I/R) injury during lung transplantation. To elucidate the mechanisms underlying hydrogen's protective effects, we conducted a gene array analysis to identify changes in gene expression associated with hydrogen treatment. Methods: Donor rats were exposed to mechanical ventilation with 98% oxygen and 2% nitrogen or 2% hydrogen for 3. h before harvest; lung grafts were stored for 4. h in cold Perfadex. Affymetrix gene array analysis of mRNA transcripts was performed on the lung tissue prior to implantation. Results: Pretreatment of donor lungs with hydrogen altered the expression of 229 genes represented on the array (182 upregulated; 47 downregulated). Hydrogen treatment induced several lung surfactant-related genes, ATP synthase genes and stress-response genes. The intracellular surfactant pool, tissue adenosine triphosphate (ATP) levels and heat shock protein 70 (HSP70) expression increased in the hydrogen-treated grafts. Hydrogen treatment also induced the transcription factors C/EBPα and C/EBPβ, which are known regulators of surfactant-related genes. Conclusion: Donor ventilation with hydrogen significantly increases expression of surfactant-related molecules, ATP synthases and stress-response molecules in lung grafts. The induction of these molecules may underlie hydrogen's protective effects against I/R injury during transplantation.
AB - Background: We previously demonstrated that donor treatment with inhaled hydrogen protects lung grafts from cold ischemia/reperfusion (I/R) injury during lung transplantation. To elucidate the mechanisms underlying hydrogen's protective effects, we conducted a gene array analysis to identify changes in gene expression associated with hydrogen treatment. Methods: Donor rats were exposed to mechanical ventilation with 98% oxygen and 2% nitrogen or 2% hydrogen for 3. h before harvest; lung grafts were stored for 4. h in cold Perfadex. Affymetrix gene array analysis of mRNA transcripts was performed on the lung tissue prior to implantation. Results: Pretreatment of donor lungs with hydrogen altered the expression of 229 genes represented on the array (182 upregulated; 47 downregulated). Hydrogen treatment induced several lung surfactant-related genes, ATP synthase genes and stress-response genes. The intracellular surfactant pool, tissue adenosine triphosphate (ATP) levels and heat shock protein 70 (HSP70) expression increased in the hydrogen-treated grafts. Hydrogen treatment also induced the transcription factors C/EBPα and C/EBPβ, which are known regulators of surfactant-related genes. Conclusion: Donor ventilation with hydrogen significantly increases expression of surfactant-related molecules, ATP synthases and stress-response molecules in lung grafts. The induction of these molecules may underlie hydrogen's protective effects against I/R injury during transplantation.
KW - Adenosine triphosphate
KW - Gene array
KW - Hydrogen
KW - Ischemia/reperfusion injury
KW - Lung surfactant
KW - Lung transplantation
UR - http://www.scopus.com/inward/record.url?scp=84865975825&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2012.08.005
DO - 10.1016/j.bbrc.2012.08.005
M3 - Article
C2 - 22902635
AN - SCOPUS:84865975825
SN - 0006-291X
VL - 425
SP - 873
EP - 879
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -