2015
DOI: 10.1016/j.ceca.2014.10.008
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The role of TRPMLs in endolysosomal trafficking and function

Abstract: Members of the Transient Receptor Potential-Mucolipin (TRPML) constitute a family of evolutionarily conserved cation channels that function predominantly in endolysosomal vesicles. Whereas loss-of-function mutations in human TRPML1 were first identified as being causative for the lysosomal storage disease, Mucolipidosis type IV, most mammals also express two other TRPML isoforms called TRPML2 and TRPML3. All three mammalian TRPMLs as well as TRPML related genes in other species including C. elegans and Drosoph… Show more

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Cited by 170 publications
(161 citation statements)
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“…26) While mutants of TRPML display severe neurodegeneration and motor deficits associated with impairment of autophagic removal of damaged mitochondria, as well as accumulation of lysosome vesicles, 27) it is unclear how rapidly these effects would incapacitate an insect if TRPML were attacked chemically.…”
Section: Trpmlmentioning
confidence: 99%
“…26) While mutants of TRPML display severe neurodegeneration and motor deficits associated with impairment of autophagic removal of damaged mitochondria, as well as accumulation of lysosome vesicles, 27) it is unclear how rapidly these effects would incapacitate an insect if TRPML were attacked chemically.…”
Section: Trpmlmentioning
confidence: 99%
“…Transient receptor potential mucolipin 1 (TRPML1) (10,(13)(14)(15) belongs to the large family of transient receptor potential ion channels that permeates Ca 2ϩ , Na ϩ , and other cations (10,(15)(16)(17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27)(28). Mutations in TRPML1 gene lead to mucolipidosis type IV (ML4) disease, which is characterized with defects in membrane trafficking in the late endocytic pathway (10,29), enlarged lysosomes (10,29), and impaired lysosome biogenesis (30 -32).…”
mentioning
confidence: 99%
“…NAADP as a potent Ca 2+ mobilizing messenger, which targets the TRPMLs or TPCs and triggers Ca 2+ release from the endolysosomal stores [19]. As we known, the members of the TRPML constitute a family of evolutionarily conserved cation channels that play crucial roles in endolysosomal vesicles [20] [49]. TRPMLs localize to endolysosomes and facilitate Ca 2+ -dependent fusion between autophagosomes and lysosomes resulting in lysosomal degradation of autophagic material [20].…”
Section: The Negative Regulation Of Cd38 In Autophagymentioning
confidence: 99%
“…As we known, the members of the TRPML constitute a family of evolutionarily conserved cation channels that play crucial roles in endolysosomal vesicles [20] [49]. TRPMLs localize to endolysosomes and facilitate Ca 2+ -dependent fusion between autophagosomes and lysosomes resulting in lysosomal degradation of autophagic material [20]. It is known that TPCs have recently emerging as the targets for NAADP, which are crucial for appropriate basal and induced autophagic flux in cardiomyocytes [50].…”
Section: The Negative Regulation Of Cd38 In Autophagymentioning
confidence: 99%