Genetic basis of age-dependent synaptic abnormalities in the retina

Hitoshi Higuchi, Erica L. Macke, Wei Hua Lee, Sam A. Miller, James C. Xu, Sakae Ikeda, Akihiro Ikeda

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Understanding the normal aging process will help us determine the mechanisms of how age-related diseases are caused and progress. A/J inbred mice have been shown to exhibit accelerated aging phenotypes in the retina including increased inflammation and photoreceptor cell degeneration, which resemble human aging symptoms. C57BL/6J (B6) inbred mice are less susceptible for these abnormalities, indicating the existence of genetic factor(s) that affect their severity. In this study, we determined that another age-dependent phenotype, ectopic synapse formation, is also accelerated in the A/J retina compared to the B6 retina. Through genetic mapping utilizing recombinant inbred strains, we identified quantitative trait loci (QTLs) on chromosome 7 and 19, which contribute to abnormal retinal synapses as well as other age-dependent phenotypes. Using consomic single chromosome substitution lines where a single chromosome is from A/J and the rest of the genome is B6, we investigated the individual effect of each QTL on retinal aging phenotypes. We observed that both QTLs independently contribute to abnormal retinal synapses, reduction in the number of cone cells, and an up-regulation of retinal stress marker, glial fibrillary acidic protein (GFAP). Mice with a single chromosome substitution on chromosome 19 also exhibited an increase in inflammatory cells, which is characteristic of aging and age-related macular degeneration. Thus, we identified QTLs that are independently capable of affecting the severity and progression of age-dependent retinal abnormalities in mice.

Original languageEnglish
Pages (from-to)21-32
Number of pages12
JournalMammalian Genome
Volume26
Issue number1-2
DOIs
Publication statusPublished - 2015
Externally publishedYes

Fingerprint

Quantitative Trait Loci
Retina
Synapses
Phenotype
Chromosomes, Human, Pair 19
Chromosomes
Inbred A Mouse
Photoreceptor Cells
Chromosomes, Human, Pair 7
Glial Fibrillary Acidic Protein
Macular Degeneration
Up-Regulation
Cell Count
Genome
Inflammation

ASJC Scopus subject areas

  • Genetics

Cite this

Higuchi, H., Macke, E. L., Lee, W. H., Miller, S. A., Xu, J. C., Ikeda, S., & Ikeda, A. (2015). Genetic basis of age-dependent synaptic abnormalities in the retina. Mammalian Genome, 26(1-2), 21-32. https://doi.org/10.1007/s00335-014-9546-7

Genetic basis of age-dependent synaptic abnormalities in the retina. / Higuchi, Hitoshi; Macke, Erica L.; Lee, Wei Hua; Miller, Sam A.; Xu, James C.; Ikeda, Sakae; Ikeda, Akihiro.

In: Mammalian Genome, Vol. 26, No. 1-2, 2015, p. 21-32.

Research output: Contribution to journalArticle

Higuchi, H, Macke, EL, Lee, WH, Miller, SA, Xu, JC, Ikeda, S & Ikeda, A 2015, 'Genetic basis of age-dependent synaptic abnormalities in the retina', Mammalian Genome, vol. 26, no. 1-2, pp. 21-32. https://doi.org/10.1007/s00335-014-9546-7
Higuchi, Hitoshi ; Macke, Erica L. ; Lee, Wei Hua ; Miller, Sam A. ; Xu, James C. ; Ikeda, Sakae ; Ikeda, Akihiro. / Genetic basis of age-dependent synaptic abnormalities in the retina. In: Mammalian Genome. 2015 ; Vol. 26, No. 1-2. pp. 21-32.
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