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Photoreceptor phagosome processing defects and disturbed autophagy in retinal pigment epithelium of Cln3Δex1-6 mice modelling juvenile neuronal ceroid lipofuscinosis (Batten disease).
- Source :
-
Human molecular genetics [Hum Mol Genet] 2015 Dec 15; Vol. 24 (24), pp. 7060-74. Date of Electronic Publication: 2015 Oct 08. - Publication Year :
- 2015
-
Abstract
- Retinal degeneration and visual impairment are the first signs of juvenile neuronal ceroid lipofuscinosis caused by CLN3 mutations, followed by inevitable progression to blindness. We investigated retinal degeneration in Cln3(Δex1-6) null mice, revealing classic 'fingerprint' lysosomal storage in the retinal pigment epithelium (RPE), replicating the human disease. The lysosomes contain mitochondrial F0-ATP synthase subunit c along with undigested membranes, indicating a reduced degradative capacity. Mature autophagosomes and basal phagolysosomes, the terminal degradative compartments of autophagy and phagocytosis, are also increased in Cln3(Δex1) (-6) RPE, reflecting disruption to these key pathways that underpin the daily phagocytic turnover of photoreceptor outer segments (POS) required for maintenance of vision. The accumulated autophagosomes have post-lysosome fusion morphology, with undigested internal contents visible, while accumulated phagosomes are frequently docked to cathepsin D-positive lysosomes, without mixing of phagosomal and lysosomal contents. This suggests lysosome-processing defects affect both autophagy and phagocytosis, supported by evidence that phagosomes induced in Cln3(Δex1) (-) (6)-derived mouse embryonic fibroblasts have visibly disorganized membranes, unprocessed internal vesicles and membrane contents, in addition to reduced LAMP1 membrane recruitment. We propose that defective lysosomes in Cln3(Δex1) (-) (6) RPE have a reduced degradative capacity that impairs the final steps of the intimately connected autophagic and phagocytic pathways that are responsible for degradation of POS. A build-up of degradative organellar by-products and decreased recycling of cellular materials is likely to disrupt processes vital to maintenance of vision by the RPE.<br /> (© The Author 2015. Published by Oxford University Press.)
- Subjects :
- Aging
Animals
Brain pathology
Disease Models, Animal
Lysosomes metabolism
Membrane Fusion
Membrane Glycoproteins genetics
Mice
Mice, Inbred C57BL
Mice, Knockout
Microspheres
Mitochondrial Proton-Translocating ATPases metabolism
Molecular Chaperones genetics
Neuronal Ceroid-Lipofuscinoses metabolism
Neurons pathology
Retinal Pigment Epithelium metabolism
Autophagy
Membrane Glycoproteins deficiency
Neuronal Ceroid-Lipofuscinoses physiopathology
Phagosomes metabolism
Retinal Pigment Epithelium physiopathology
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2083
- Volume :
- 24
- Issue :
- 24
- Database :
- MEDLINE
- Journal :
- Human molecular genetics
- Publication Type :
- Academic Journal
- Accession number :
- 26450516
- Full Text :
- https://doi.org/10.1093/hmg/ddv406