Mitochondrial damage-induced impairment of angiogenesis in the aging rat kidney.

Abstract

Decreased expression of vascular endothelial growth factor (VEGF) in the renal tubules is thought to cause progressive loss of the renal microvasculature with age. Mitochondrial dysfunction may be a principal phenomenon underlying the process of aging. The relation between VEGF expression and mitochondrial dysfunction in aging is not fully understood. We hypothesized that mitochondrial dysfunction blocks VEGF expression and contributes to impaired angiogenesis in the aging kidney. The aim of this study was to assess the role of mitochondria in VEGF expression in the aging rat kidney. We evaluated the accumulation of 8-hydroxy-2'-deoxyguanosine in mitochondrial DNA, as well as mitochondrial dysfunction, as assessed by electron microscopy of mitochondrial structure and histochemical staining for respiratory chain complex IV, in aging rat kidney. An increase in hypoxic area and a decrease in peritubular capillaries were detected in the cortex of aging rat kidneys; however, upregulation of VEGF expression was not observed. The expression of VEGF in proximal tubular epithelial cells in response to hypoxia was suppressed by the mitochondrial electron transfer inhibitor myxothiazol. Mitochondrial DNA-deficient cells also failed to upregulate VEGF expression under hypoxic conditions. These results indicate that impairment of VEGF upregulation, possibly as a result of mitochondrial dysfunction, contributes to impaired angiogenesis, which in turn leads to renal injury in the aging rat kidney.

• Authors: Minoru Satoh, Sohachi Fujimoto, Hideyuki Horike, Masahito Ozeki, Hajime Nagasu, Naruya Tomita, Tamaki Sasaki, Naoki Kashihara
• Journal: Laboratory investigation; a journal of technical methods and pathology (Lab Invest) Vol. 91 Issue 2 Pg. 190-202 (Feb 2011) ISSN: 1530-0307 [Electronic] United States
• PMID: 20921951 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• DNA Primers
• Methacrylates
• Thiazoles
• Vascular Endothelial Growth Factor A
• myxothiazol
• 8-Hydroxy-2'-Deoxyguanosine
• Deoxyguanosine

Topics

• 8-Hydroxy-2'-Deoxyguanosine
• Aging (physiology)
• Animals
• DNA Primers (genetics)
• Deoxyguanosine (analogs & derivatives, metabolism)
• Enzyme-Linked Immunosorbent Assay
• Gene Expression Regulation (drug effects, physiology)
• Immunohistochemistry
• Kidney Tubules, Proximal (drug effects, metabolism, physiopathology)
• Male
• Methacrylates (pharmacology)
• Microscopy, Electron
• Mitochondria (metabolism, ultrastructure)
• Neovascularization, Physiologic (physiology)
• Oligonucleotide Array Sequence Analysis
• Rats
• Rats, Wistar
• Reverse Transcriptase Polymerase Chain Reaction
• Thiazoles (pharmacology)
• Vascular Endothelial Growth Factor A (metabolism)