Species-specific ultrastructure of neuronal lipofuscin in hippocampus and neocortex of subhuman mammals and humans.
Abstract: Lipofuscin represents an integral part of neurons and glial cells in mammals and in submammalian species. It is a special lysosomal organelle, takes part of cellular metabolism, and is a structural expression of catabolic pathways. Species-specific differences of lipofuscin indicate metabolic differences of the relevant neurons. The authors have studied the ultrastructure of neuronal lipofuscin in the hippocampus and cerebral neocortex of dogs, horses, cows, elephants, rats, mice, apes, and humans to answer the question of species-specific differences of this organelle. Paraffin sections of formalin-fixed material were investigated by hematoxylin-eosin and PAS staining, by fluorescence microscopy for autofluorescence, with a laser scanning confocal microscope and by electron microscopy. In the animals studied and in humans the lipofuscin displayed, in addition to the general trilaminar substructure, species-specific appearances. No differences were found in the lipofuscin structure between neocortical and hippocampal neurons of the separate animal species. In contrast, in humans, neurons of the hippocampus showed a particular lipofuscin structure, not only different from the neocortical one, but also with differences between CA1 and CA3/4 sectors. Interestingly, in apes a transitional situation was found with slight differences between neocortical and hippocampal lipofuscin, especially in the rhesus monkey. This peculiarity was corroborated by the distribution of special pentilaminar linear structures in the lipofuscin pigment in all animals, only sparsely in the rhesus monkey and not in humans. The results indicate that lipofuscin ultrastructure of neocortical and hippocampal neurons is species specific and that lipofuscin in the human hippocampal neurons displays structures characteristic of man differing from the neocortical neuronal lipofuscin. The neuronal lipofuscin of apes, especially of the rhesus monkey displays structures in between humans and lower mammals. Nothing is known about the functional significance of these findings. They may indicate metabolic and/or functional characteristics of the relevant neurons.
Publication Date: 2005-03-15 PubMed ID: 15764582DOI: 10.1080/019131290882330Google Scholar: Lookup
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- Comparative Study
- Journal Article
Summary
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The research article investigates the unique characteristics and variations of lipofuscin—a cellular component found in neurons—in different species (like dogs, horses, cows, elephants, rats, mice, apes, and humans). The researchers discovered that the structure of lipofuscin varies between species and even between different parts of the human brain, hinting at the difference in the metabolic processes and functional traits of these neurons.
Methodology
- Researchers examined the ultrastructure (complex structures visible at the electron microscope level) of neuronal lipofuscin in various species. These species included various animals (dogs, horses, cows, elephants, rats, mice, apes,) including humans.
- Formalin-fixed material—paraffin sections—was used as the sample for this study.
- The researchers devised several staining techniques (including hematoxylin-eosin and PAS staining), fluorescence microscopy for autofluorescence, laser scanning confocal microscopy, and electron microscopy to investigate the sample’s ultrastructure.
Findings
- The study found that lipofuscin exhibited a trilaminar substructure (a three-layered structure) and additional species-specific structures.
- No significant differences were discovered between the lipofuscin structure in neocortical and hippocampal neurons within the same species of animals.
- Different outcomes were found in humans – hippocampal neurons showed a unique lipofuscin structure, varying not only from human neocortical neurons but also within different sectors of the hippocampus (between CA1 and CA3/4 sectors).
- Apes exhibited a transitional situation with minimal differences between lipofuscin structures in neocortical and hippocampal neurons, particularly in rhesus monkeys.
- A distribution of pentilaminar linear structures was identified within the lipofuscin pigment across all animal species, with sparse appearances in rhesus monkeys and none in humans.
Conclusions
- The study concludes that the ultrastructure of lipofuscin in neocortical and hippocampal neurons varies across species.
- In humans, lipofuscin in the hippocampal neurons demonstrates unique structures that differ from the neocortical neurons. This unique structure wasn’t observed in other animals, indicating this might be a specific characteristic in humans.
- The lipofuscin in apes, particularly the rhesus monkey, exhibits characteristics somewhat intermediate between humans and lower mammals.
- However, the functional implication of these variations in lipofuscin structure remains unknown. It is speculated that this might indicate the different metabolic and functional properties of the related neurons.
Cite This Article
APA
Boellaard JW, Schlote W, Hofer W.
(2005).
Species-specific ultrastructure of neuronal lipofuscin in hippocampus and neocortex of subhuman mammals and humans.
Ultrastruct Pathol, 28(5-6), 341-351.
https://doi.org/10.1080/019131290882330 Publication
Researcher Affiliations
- Institut für Hirnforschung der Universität Tübingen, Tübingen, Germany.
MeSH Terms
- Adult
- Animals
- Cattle
- Dogs
- Hippocampus / metabolism
- Hippocampus / ultrastructure
- Humans
- Lipofuscin / metabolism
- Mammals / anatomy & histology
- Mammals / metabolism
- Mice
- Microscopy, Confocal
- Microscopy, Electron, Transmission
- Neocortex / metabolism
- Neocortex / ultrastructure
- Neurons / metabolism
- Neurons / ultrastructure
- Periodic Acid-Schiff Reaction
- Rats
- Rats, Sprague-Dawley
- Species Specificity
Citations
This article has been cited 8 times.- Adeniyi PA, Fopiano KA, Banine F, Garcia M, Gong X, Keene CD, Sherman LS, Bagi Z, Back SA. Multispectral LEDs Eliminate Lipofuscin-Associated Autofluorescence for Immunohistochemistry and CD44 Variant Detection by in Situ Hybridization in Aging Human, non-Human Primate, and Murine Brain.. ASN Neuro 2022 Jan-Dec;14:17590914221123138.
- Račková L, Csekes E. Proteasome Biology: Chemistry and Bioengineering Insights.. Polymers (Basel) 2020 Dec 4;12(12).
- Perens J, Salinas CG, Skytte JL, Roostalu U, Dahl AB, Dyrby TB, Wichern F, Barkholt P, Vrang N, Jelsing J, Hecksher-Sørensen J. An Optimized Mouse Brain Atlas for Automated Mapping and Quantification of Neuronal Activity Using iDISCO+ and Light Sheet Fluorescence Microscopy.. Neuroinformatics 2021 Jul;19(3):433-446.
- Zucca FA, Vanna R, Cupaioli FA, Bellei C, De Palma A, Di Silvestre D, Mauri P, Grassi S, Prinetti A, Casella L, Sulzer D, Zecca L. Neuromelanin organelles are specialized autolysosomes that accumulate undegraded proteins and lipids in aging human brain and are likely involved in Parkinson's disease.. NPJ Parkinsons Dis 2018;4:17.
- Hainsworth AH, Lee S, Foot P, Patel A, Poon WW, Knight AE. Super-resolution imaging of subcortical white matter using stochastic optical reconstruction microscopy (STORM) and super-resolution optical fluctuation imaging (SOFI).. Neuropathol Appl Neurobiol 2018 Jun;44(4):417-426.
- Riew TR, Kim HL, Choi JH, Jin X, Shin YJ, Lee MY. Progressive accumulation of autofluorescent granules in macrophages in rat striatum after systemic 3-nitropropionic acid: a correlative light- and electron-microscopic study.. Histochem Cell Biol 2017 Nov;148(5):517-528.
- Tanaka Y, Chambers JK, Matsuwaki T, Yamanouchi K, Nishihara M. Possible involvement of lysosomal dysfunction in pathological changes of the brain in aged progranulin-deficient mice.. Acta Neuropathol Commun 2014 Jul 15;2:78.
- Petty HR, Elner VM, Kawaji T, Clark A, Thompson D, Yang DL. A facile method for immunofluorescence microscopy of highly autofluorescent human retinal sections using nanoparticles with large Stokes shifts.. J Neurosci Methods 2010 Aug 30;191(2):222-6.
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