Free Access
Issue
Med Sci (Paris)
Volume 27, Number 2, Février 2011
Page(s) 153 - 162
Section M/S revues
DOI https://doi.org/10.1051/medsci/2011272153
Published online 08 March 2011
  1. Ebanks JP, Wickett RR, Boissy RE. Mechanisms regulating skin pigmentation: the rise and fall of complexion coloration. Int J Mol Sci 2009 ; 10 : 4066-4087. [CrossRef] [PubMed] [Google Scholar]
  2. Seiji M, Fitzpatrick TM, Simpson RT, Birbeck MSC. Chemical composition and terminology of specialized organelles (melanosomes and melanin granules) in mammalian melanocytes. Nature 1963 ; 197 : 1082-1084. [CrossRef] [PubMed] [Google Scholar]
  3. Raposo G, Tenza D, Murphy DM, et al.. Distinct protein sorting and localization to premelanosomes, melanosomes, and lysosomes in pigmented melanocytic cells. J Cell Biol 2001 ; 152 : 809-824. [CrossRef] [PubMed] [Google Scholar]
  4. Raposo G, Marks MS. Melanosomes--dark organelles enlighten endosomal membrane transport. Nat Rev Mol Cell Biol 2007 ; 8 : 786-797. [CrossRef] [PubMed] [Google Scholar]
  5. Kushimoto T, Basrur V, Valencia J, et al. A model for melanosome biogenesis based on the purification and analysis of early melanosomes. Proc Natl Acad Sci USA 2001 ; 98 : 10698-10703. [CrossRef] [Google Scholar]
  6. Yasumoto K, Watabe H, Valencia JC, et al. Epitope mapping of the melanosomal matrix protein gp100 (PMEL17): rapid processing in the endoplasmic reticulum and glycosylation in the early Golgi compartment. J Biol Chem 2004 ; 279 : 28330-28338. [CrossRef] [PubMed] [Google Scholar]
  7. Berson JF, Harper DC, Tenza D, et al. Pmel17 initiates premelanosome morphogenesis within multivesicular bodies. Mol Biol Cell 2001 ; 12 : 3451-3464. [PubMed] [Google Scholar]
  8. Gould GW, Lippincott-Schwartz J. New roles for endosomes: from vesicular carriers to multi-purpose platforms. Nat Rev Mol Cell Biol 2009 ; 10 : 287-292. [CrossRef] [PubMed] [Google Scholar]
  9. Simons M, Raposo G. Exosomes-vesicular carriers for intercellular communication. Curr Opin Cell Biol 2009 ; 21 : 575-581. [CrossRef] [PubMed] [Google Scholar]
  10. Fowler DM, Koulov AV, Alory-Jost C, et al. Functional amyloid formation within mammalian tissue. PLoS Biol 2006 ; 4 : e6. [CrossRef] [PubMed] [Google Scholar]
  11. Watt B, van Niel G, Fowler DM, et al. N-terminal domains elicit formation of functional Pmel17 amyloid fibrils. J Biol Chem 2009 ; 284 : 35543-35555. [CrossRef] [PubMed] [Google Scholar]
  12. Berson JF, Theos AC, Harper DC, et al. Proprotein convertase cleavage liberates a fibrillogenic fragment of a resident glycoprotein to initiate melanosome biogenesis. J Cell Biol 2003 ; 161 : 521-533. [CrossRef] [PubMed] [Google Scholar]
  13. Hurbain I, Geerts WJ, Boudier T, et al. Electron tomography of early melanosomes: implications for melanogenesis and the generation of fibrillar amyloid sheets. Proc Natl Acad Sci USA 2008 ; 105 : 19726-19731. [CrossRef] [Google Scholar]
  14. Theos AC, Truschel ST, Tenza D, et al. A lumenal domain-dependent pathway for sorting to intralumenal vesicles of multivesicular endosomes involved in organelle morphogenesis. Dev Cell 2006 ; 10 : 343-354. [CrossRef] [PubMed] [Google Scholar]
  15. Roxrud I, Stenmark H, Malerod L. ESCRT and Co. Biol Cell 2010 ; 102 : 293-318. [CrossRef] [PubMed] [Google Scholar]
  16. Wei ML. Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function. Pigment Cell Res 2006 ; 19 : 19-42. [CrossRef] [PubMed] [Google Scholar]
  17. Theos AC, Tenza D, Martina JA, et al. Functions of AP-3 and AP-1 in Tyrosinase Sorting from Endosomes to Melanosomes. Mol Biol Cell 2005 ; 16 : 5356-5372. [CrossRef] [PubMed] [Google Scholar]
  18. Gautam R, Novak EK, Tan J, et al. Interaction of Hermansky-Pudlak Syndrome genes in the regulation of lysosome-related organelles. Traffic 2006 ; 7 : 779-792. [CrossRef] [PubMed] [Google Scholar]
  19. Delevoye C, Hurbain I, Tenza D, et al. AP-1 and KIF13A coordinate endosomal sorting and positioning during melanosome biogenesis. J Cell Biol 2009 ; 187 : 247-264. [CrossRef] [PubMed] [Google Scholar]
  20. Bonifacino JS, Traub LM. Signals for sorting of transmembrane proteins to endosomes and lysosomes. Annu Rev Biochem 2003 ; 72 : 395-447. [CrossRef] [PubMed] [Google Scholar]
  21. Oetting WS, Fryer JP, Shriram S, King RA. Oculocutaneous albinism type 1: the last 100 years. Pigment Cell Res 2003 ; 16 : 307-311. [CrossRef] [PubMed] [Google Scholar]
  22. Setty SR, Tenza D, Sviderskaya EV, et al. Cell-specific ATP7A transport sustains copper-dependent tyrosinase activity in melanosomes. Nature 2008 ; 454 : 1142-1146. [CrossRef] [PubMed] [Google Scholar]
  23. Setty SR, Tenza D, Truschel ST, et al.. BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles. Mol Biol Cell 2007 ; 18 : 768-780. [CrossRef] [PubMed] [Google Scholar]
  24. Di Pietro SM, Falcon-Perez JM, Tenza D, et al. BLOC-1 interacts with BLOC-2 and the AP-3 complex to facilitate protein trafficking on endosomes. Mol Biol Cell 2006 ; 17 : 4027-4038. [CrossRef] [PubMed] [Google Scholar]
  25. Salazar G, Craige B, Styers ML, et al. BLOC-1 complex deficiency alters the targeting of adaptor protein complex-3 cargoes. Mol Biol Cell 2006 ; 17 : 4014-4026. [CrossRef] [PubMed] [Google Scholar]
  26. Di Pietro SM, Falcon-Perez JM, Dell’Angelica EC. Characterization of BLOC-2, a complex containing the Hermansky-Pudlak syndrome proteins HPS3, HPS5 and HPS6. Traffic 2004 ; 5 : 276-283. [CrossRef] [PubMed] [Google Scholar]
  27. Gautam R, Chintala S, Li W, et al. The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2). J Biol Chem 2004 ; 279 : 12935-12942. [CrossRef] [PubMed] [Google Scholar]
  28. Boissy RE, Richmond B, Huizing M, et al. Melanocyte-specific proteins are aberrantly trafficked in melanocytes of Hermansky-Pudlak syndrome-type 3. Am J Pathol 2005 ; 166 : 231-240. [CrossRef] [PubMed] [Google Scholar]
  29. Martens S, McMahon HT. Mechanisms of membrane fusion: disparate players and common principles. Nat Rev Mol Cell Biol 2008 ; 9 : 543-556. [CrossRef] [PubMed] [Google Scholar]
  30. Wade N, Bryant NJ, Connolly LM, et al. Syntaxin 7 complexes with mouse Vps10p tail interactor 1b, Syntaxin 6, vesicle-associated membrane protein (VAMP)8, and VAMP7 in B16 melanoma cells. J Biol Chem 2001 ; 276 : 19820-19827. [CrossRef] [PubMed] [Google Scholar]
  31. Huang L, Kuo YM, Gitschier J. The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency. Nat Genet 1999 ; 23 : 329-332. [CrossRef] [PubMed] [Google Scholar]
  32. Prekeris R, Klumperman J, Chen YA, Scheller RH. Syntaxin 13 mediates cycling of plasma membrane proteins via tubulovesicular recycling endosomes. J Cell Biol 1998 ; 143 : 957-971. [CrossRef] [PubMed] [Google Scholar]
  33. Dell’Angelica EC, Aguilar RC, Wolins N, et al. Molecular characterization of the protein encoded by the Hermansky-Pudlak syndrome type 1 gene. J Biol Chem 2000 ; 275 : 1300-1306. [CrossRef] [PubMed] [Google Scholar]
  34. Bassi MT, Bergen AA, Bitoun P, et al.. Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America. Hum Genet 2001 ; 108 : 51-54. [CrossRef] [PubMed] [Google Scholar]
  35. Schiaffino MV. Signaling pathways in melanosome biogenesis and pathology. Int J Biochem Cell Biol 2010 ; 42 : 1094-1104. [CrossRef] [PubMed] [Google Scholar]
  36. Innamorati G, Piccirillo R, Bagnato P, et al. The melanosomal/lysosomal protein OA1 has properties of a G protein-coupled receptor. Pigment Cell Res 2006 ; 19 : 125-135. [CrossRef] [PubMed] [Google Scholar]
  37. Lopez VM, Decatur CL, Stamer WD, Lynch RM, McKay BS. L-DOPA is an endogenous ligand for OA1. PLoS Biol 2008 ; 6 : e236. [CrossRef] [PubMed] [Google Scholar]
  38. Giordano F, Bonetti C, Surace EM, et al. The ocular albinism type 1 (OA1) G-protein-coupled receptor functions with MART-1 at early stages of melanogenesis to control melanosome identity and composition. Hum Mol Genet 2009 ; 18 : 4530-4545. [CrossRef] [PubMed] [Google Scholar]
  39. Piccirillo R, Palmisano I, Innamorati G, et al. An unconventional dileucine-based motif and a novel cytosolic motif are required for the lysosomal and melanosomal targeting of OA1. J Cell Sci 2006 ; 119 : 2003-2014. [CrossRef] [PubMed] [Google Scholar]
  40. Young A, Powelson EB, Whitney IE, et al. Involvement of OA1, an intracellular GPCR, and G alpha i3, its binding protein, in melanosomal biogenesis and optic pathway formation. Invest Ophthalmol Vis Sci 2008 ; 49 : 3245-3252. [CrossRef] [PubMed] [Google Scholar]
  41. Fitzpatrick TB, Breathnach AS. The epidermal melanin unit system. Dermatol Wochenschr 1963 ; 147 : 481-489. [PubMed] [Google Scholar]
  42. Van Den Bossche K, Naeyaert JM, Lambert J. The quest for the mechanism of melanin transfer. Traffic 2006 ; 7 : 769-778. [CrossRef] [PubMed] [Google Scholar]
  43. Hara M, Yaar M, Byers HR, et al. Kinesin participates in melanosomal movement along melanocyte dendrites. J Invest Dermatol 2000 ; 114 : 438-443. [CrossRef] [PubMed] [Google Scholar]
  44. Seabra MC, Coudrier E. Rab GTPases and myosin motors in organelle motility. Traffic 2004 ; 5 : 393-399. [CrossRef] [PubMed] [Google Scholar]
  45. Bahadoran P, Ortonne J, Ballotti R. Que trafiquent les mélanosomes ? Med Sci (Paris) 2002 ; 18 : 205-209. [CrossRef] [EDP Sciences] [Google Scholar]
  46. Gudbjartsson DF, Sulem P, Stacey SN, et al. ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma. Nat Genet 2008 ; 40 : 886-891. [CrossRef] [PubMed] [Google Scholar]
  47. Kummer MP, Maruyama H, Huelsmann C, et al. Formation of Pmel17 amyloid is regulated by juxtamembrane metalloproteinase cleavage, and the resulting C-terminal fragment is a substrate for gamma-secretase. J Biol Chem 2009 ; 284 : 2296-2306. [CrossRef] [PubMed] [Google Scholar]
  48. Ehehalt R, Keller P, Haass C, et al. Amyloidogenic processing of the Alzheimer beta-amyloid precursor protein depends on lipid rafts. J Cell Biol 2003 ; 160 : 113-123. [CrossRef] [PubMed] [Google Scholar]
  49. Yamaguchi Y, Brenner M, Hearing VJ. The regulation of skin pigmentation. J Biol Chem 2007 ; 282 : 27557-27561. [CrossRef] [PubMed] [Google Scholar]
  50. Incerti B, Cortese K, Pizzigoni A, et al. Oa1 knock-out: new insights on the pathogenesis of ocular albinism type 1. Hum Mol Genet 2000 ; 9 : 2781-2788. [CrossRef] [PubMed] [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.