Purpose: To examine the ultrastructure of lipofuscin bodies and melanosomes in retinal epithelium of elderly rhesus monkeys and determines changes in their number and morphology as a function of retinal eccentricity.

Methods: Electron microscopy was used to describe and quantify two major organelles in elderly monkey retinal epithelium, lipofuscin bodies and melanosomes, at different retinal loci extending from the macula to the peri-macula, equator, periphery and ora serrata. Osmium tetroxide was used to distinguish lipofuscin bodies from melanosomes.

Results: Lipofuscin bodies and melanosomes diminished in number with advanced age but there was an inverse relationship between these two organelles. Lipofuscin bodies were more numerous in the macula and melanosomes more numerous in the peripheral retina. Three types of lipofuscin bodies were identified: 1) smaller and tending to locate in the middle third of the epithelial cell, 2) larger, less common, and located more basally, and 3) extremely rare, melano-lipofuscin, containing a melanosome. When osmicated, all lipofuscin bodies contained electron dense materials. When osmium tetroxide was not used for fixation, the first two types of lipofuscin bodies lost their electron densities while the third type retained its electron density due to the melanosome it contained.

Conclusion: As previously reported for human retina, lipofuscin is most abundant in the macular and peri-macular epithelium and least abundant in the periphery, whereas melanosomes show the opposite relationship. This distribution pattern could contribute to the macula's greater vulnerability to photo-toxicity. Three types of lipofuscin bodies are found in aging monkey retinal epithelium. All types contain electron dense material, but the most prominent two types lose their densities in the absence of osmium tetroxide during fixation. Most of the electron densities in lipofuscin bodies must contain a material that binds strongly to osmium tetroxide such as polyunsaturated fatty acids.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6141211PMC
http://dx.doi.org/10.1080/02713683.2018.1464194DOI Listing

Publication Analysis

Top Keywords

lipofuscin bodies
40
osmium tetroxide
20
retinal epithelium
16
lipofuscin
12
monkey retinal
12
bodies melanosomes
12
types lipofuscin
12
bodies
10
aging monkey
8
melanosomes retinal
8

Similar Publications

Neuronal ceroid lipofuscinosis type 2 (CLN2) results from biallelic pathogenic variants in the gene, leading to deficient activity of the lysosomal enzyme tripeptidyl peptidase 1. We report an autopsy case of CLN2 characterized at molecular level. The patient exhibited a spectrum of neurologic symptoms including epilepsy, behavioral alterations, cognitive regression, motor impairment, and visual loss.

View Article and Find Full Text PDF

Comparative analysis of the color change in blue-green inclusions within neutrophils between two patients with different clinical outcomes.

Biochem Med (Zagreb)

October 2024

Department of Laboratory Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.

Article Synopsis
  • Blue-green neutrophilic inclusions (BGNI), linked to serious conditions like acute liver failure and lactic acidosis, appear as bright green structures in neutrophils and can indicate a poor prognosis.
  • Two case studies were presented: one involving a patient with a bunyavirus infection and severe liver damage who deteriorated despite treatment, and another who experienced liver injury from wasp stings but ultimately recovered.
  • The study observed that an increase in BGNI quantity and deepening color signaled worsening health in the first case, while a decrease and lightening color suggested improvement in the second case, highlighting a potential prognostic value of BGNI characteristics.
View Article and Find Full Text PDF
Article Synopsis
  • - VPS35, a key protein in the retromer complex that helps regulate endosomal trafficking, is genetically linked to Parkinson's disease and is associated with visual impairment in affected individuals.
  • - Research findings show that mouse retinas lacking VPS35 exhibit significant synapse loss, vision deficits, and progressive degeneration tied to the formation of Lewy body-like inclusions and aggregation of a protein called phospho-α-synuclein (P-αSyn).
  • - The study reveals that VPS35 interacts with another protein, HSC70, and a deficiency in VPS35 leads to the accumulation of aggregates in late endosomes, activating microglia which can be seen in live imaging as bright dots, marking the onset of pathology
View Article and Find Full Text PDF

Neuronal Ceroid Lipofuscinosis in a Mixed-Breed Dog with a Splice Site Variant in .

Genes (Basel)

May 2024

Canine Genetics Laboratory, Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA.

A 23-month-old neutered male dog of unknown ancestry presented with a history of progressive neurological signs that included anxiety, cognitive impairment, tremors, seizure activity, ataxia, and pronounced visual impairment. The clinical signs were accompanied by global brain atrophy. Due to progression in the severity of disease signs, the dog was euthanized at 26 months of age.

View Article and Find Full Text PDF

Huntington's disease (HD) is caused by expansion of the polyglutamine stretch in huntingtin protein (HTT) resulting in hallmark aggresomes/inclusion bodies (IBs) composed of mutant huntingtin protein (mHTT) and its fragments. Stimulating autophagy to enhance mHTT clearance is considered a potential therapeutic strategy for HD. Our recent evaluation of the autophagic-lysosomal pathway (ALP) in human HD brain reveals upregulated lysosomal biogenesis and relatively normal autophagy flux in early Vonsattel grade brains, but impaired autolysosome clearance in late grade brains, suggesting that autophagy stimulation could have therapeutic benefits as an earlier clinical intervention.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!