Relative quantification of white blood cell mitochondrial DNA and assessment of mitochondria by use of transmission electron microscopy in English Springer Spaniels with and without retinal dysplasia.

OBJECTIVE To compare relative amounts of WBC mitochondrial DNA (mtDNA; assessed via real-time PCR assay) and morphology of lymphocyte mitochondria (assessed via transmission electron microscopy [TEM]) in blood samples collected from English Springer Spaniels with and without retinal dysplasia. ANIMALS 7 and 5 client-owned English Springer Spaniels (1 to 11 years old) with and without retinal dysplasia, respectively. PROCEDURES Blood samples were obtained from affected and unaffected dogs via venipuncture. Genomic DNA was extracted from WBCs of the 7 affected and 5 unaffected dogs, and relative quantification of the cytochrome c oxidase subunit 1 gene (COX1) was determined via analysis of real-time PCR results. White blood cells from 3 affected and 4 unaffected dogs were embedded in epoxide resin for TEM; cross sections were examined for lymphocytes, which were measured. The mitochondria within lymphocytes were quantified, and the mitochondrial surface area per lymphocyte cross section was calculated. A masked technique was used to compare mitochondrial morphology between the 2 groups. RESULTS Compared with the smallest measured quantity of mtDNA among unaffected dogs, mtDNA amounts varied among unaffected (1.08- to 4.76-fold differences) and affected dogs (1- to 2.68-fold differences). Analysis of lymphocyte measurements and mitochondrial surface area, morphology, and quantity revealed no significant differences between affected and unaffected dogs. CONCLUSIONS AND CLINICAL RELEVANCE No significant differences were detected in relative amounts of WBC mtDNA or the size, number, or morphology of lymphocyte mitochondria in English Springer Spaniels affected with retinal dysplasia, compared with results for unaffected control dogs.

[1]  A. Galinier,et al.  Physiological diversity of mitochondrial oxidative phosphorylation. , 2006, American journal of physiology. Cell physiology.

[2]  G. Appleyard,et al.  Differential mitochondrial DNA and gene expression in inherited retinal dysplasia in miniature Schnauzer dogs. , 2006, Investigative ophthalmology & visual science.

[3]  R. Iida,et al.  Quantitative change in mitochondrial DNA content in various mouse tissues during aging. , 2005, Biochimica et biophysica acta.

[4]  Yau-Huei Wei,et al.  Alteration of the Copy Number of Mitochondrial DNA in Leukocytes of Patients with Hyperlipidemia , 2005, Annals of the New York Academy of Sciences.

[5]  Yau-Huei Wei,et al.  Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. , 2005, The international journal of biochemistry & cell biology.

[6]  B. Grahn,et al.  Inherited retinal dysplasia and persistent hyperplastic primary vitreous in Miniature Schnauzer dogs. , 2004, Veterinary ophthalmology.

[7]  Chin-San Liu,et al.  Oxidative Stress-related Alteration of the Copy Number of Mitochondrial DNA in Human Leukocytes , 2003, Free radical research.

[8]  S. Welle,et al.  Reduced amount of mitochondrial DNA in aged human muscle. , 2003, Journal of applied physiology.

[9]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[10]  V. Pesce,et al.  Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle. , 2001, Free radical biology & medicine.

[11]  M. Pfaffl,et al.  A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.

[12]  A. M. van der Bliek,et al.  The Many Shapes of Mitochondrial Membranes , 2001, Traffic.

[13]  C. Graff,et al.  Impaired insulin secretion and β-cell loss in tissue-specific knockout mice with mitochondrial diabetes , 2000, Nature Genetics.

[14]  K. Nair,et al.  Effects of Aging on Mitochondrial DNA Copy Number and Cytochromec Oxidase Gene Expression in Rat Skeletal Muscle, Liver, and Heart* , 2000, The Journal of Biological Chemistry.

[15]  H. C. Lee,et al.  Aging‐ and smoking‐associated alteration in the relative content of mitochondrial DNA in human lung , 1998, FEBS letters.

[16]  G. Barsh,et al.  Mitochondrial transcription factor A is necessary for mtDNA maintance and embryogenesis in mice , 1998, Nature Genetics.

[17]  X. Estivill,et al.  Reduced steady-state levels of mitochondrial RNA and increased mitochondrial DNA amount in human brain with aging. , 1997, Brain research. Molecular brain research.

[18]  X. Estivill,et al.  Qualitative and quantitative changes in skeletal muscle mtDNA and expression of mitochondrial-encoded genes in the human aging process. , 1997, Biochemical and molecular medicine.

[19]  V. Dubowitz,et al.  Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion. , 1994, Human molecular genetics.

[20]  H. Dekker,et al.  Mitochondria in cultured human muscle cells depleted of mitochondrial DNA. , 1993, European Journal of Cell Biology.

[21]  H. Whiteley Dysplastic canine retinal morphogenesis. , 1991, Investigative ophthalmology & visual science.

[22]  G. A. Severin,et al.  Retinal Dysplasia of English Springer Spaniel Dogs: Light Microscopy of the Postnatal Lesions , 1983, Veterinary pathology.

[23]  Romano Pe,et al.  Association for Research in Vision and Ophthalmology. , 2000 .

[24]  H. Whiteley,et al.  Intramembranous particle distribution and filipin binding in dysplastic canine retina. , 1991, Current eye research.

[25]  H. Whiteley,et al.  The external limiting membrane in developing normal and dysplastic canine retina. , 1986, Tissue & cell.