Robust Lysosomal Calcium Signaling Through Channel TRPML1 is Impaired by Lysosomal Lipid Accumulation

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Penn collection
Departmental Papers (Dental)
Degree type
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Subject
Calcium signaling
Cellular aging
Lysosomal storage disease
Mucolipin
RPE
Animals
Calcium
Calcium Signaling
Cell Line
Disease Models
Animal
Humans
Lipid Metabolism
Lysosomes
Macular Degeneration
Mice
Mice
Knockout
Phthalimides
Quinolines
Retinal Pigment Epithelium
Transient Receptor Potential Channels
bafilomycin
chloroquine
desipramine
filipin
ml sa 1
sphingomyelin
thapsigargin
transient receptor potential cation channel mucolipin 1
transient receptor potential channel
transient receptor potential channel affecting agent
unclassified drug
calcium
MCOLN1 protein
human
Mcoln1 protein
mouse
ML-SA1 compound
phthalimide derivative
quinoline derivative
transient receptor potential channel
animal cell
ARPE-19 cell line
Article
autofluorescence
calcium signaling
calcium transport
controlled study
embryo
endoplasmic reticulum
extracellular calcium
human
human cell
lipid peroxidation
lipid storage
lysosome
mouse
nonhuman
priority journal
retina degeneration
Stargardt disease
agonists
animal
cell line
disease model
genetics
knockout mouse
lipid metabolism
lysosome
macular degeneration
metabolism
pathology
retinal pigment epithelium
Dentistry
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Gomez, Nestor Mas
Lu, Wennan
Lim, Jason C.
Kiselyov, Kirill
Campagno, Keith E.
Campagno, Yulia
Slaugenhaupt, Susan A.
Pfeffer, Bruce A.
Fliesler, Steven J.
Mitchell, Claire H.
Contributor
Abstract

The transient receptor potential cation channelmucolipin 1 (TRPML1) channel is a conduit for lysosomal calcium efflux, and channel activity may be affected by lysosomal contents. The lysosomes of retinal pigmented epithelial (RPE) cells are particularly susceptible to build-up of lysosomal waste products because they must degrade the outer segments phagocytosed daily from adjacent photoreceptors; incomplete degradation leads to accumulation of lipid waste in lysosomes. This study asks whether stimulation of TRPML1 can release lysosomal calciuminRPE cells andwhether such release is affectedby lysosomal accumulations.The TRPM LagonistML-SA1 raised cytoplasmic calcium levels in mouse RPE cells, hesRPE cells, and ARPE-19 cells; this increase was rapid, robust, reversible, and reproducible. The increase was not altered by extracellular calcium removal or by thapsigargin but was eliminated by lysosomal rupture with glycyl-L-phenylalanine-b-naphthylamide. Treatment with desipramine toinhibit acidsphingomyelinase orYM201636 to inhibitPIKfyve also reducedthe cytoplasmic calcium increase triggered by ML-SA1, whereas RPE cells from TRPML-/- mice showed no response to ML-SA1. Cotreatmentwith chloroquine and U18666A induced formation of neutral, autofluorescent lipid in RPE lysosomes and decreased lysosomalCa2+ release.LysosomalCa2+ releasewas also impaired in RPEcells from the ATP-binding cassette, subfamily A, member 4-/-mouse model of Stargardt's retinal dystrophy. Neither TRPML1 mRNA nor total lysosomal calcium levels were altered in these models,suggesting a more direct effect on the channel. In summary, stimulation of TRPML1 elevates cytoplasmic calciumlevels in RPE cells, but this response is reduced by lysosomal accumulation.-Gomez, N. M.,Lu,W.Lim, J. C.,Kiselyov, K.,Campagno, K.E.,Grishchuk,Y., Slaugenhaupt, S. A., Pfeffer, B., Fliesler, S. J., Mitchell, C. H. Robust lysosomal calcium signaling through channel TRPML1 is impaired by lysosomal lipid accumulation. FASEB J. 32, 782-794 (2018). www.fasebj.org. © FASEB.

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2018-02-01
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FASEB Journal
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Open access version of the article downloaded from PubMed Central. PMCID: PMC5888396
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