Secretory lysosomes

Regulated secretion of stored secretory products is important in many cell types. In contrast to professional secretory cells, which store their secretory products in specialized secretory granules, some secretory cells store their secretory proteins in a dual-function organelle, called a secretory lysosome. Functionally, secretory lysosomes are unusual in that they serve both as a degradative and as a secretory compartment. Recent work shows that cells with secretory lysosomes use new sorting and secretory pathways. The importance of these organelles is highlighted by several genetic diseases, in which immune function and pigmentation — two processes that normally involve secretory lysosomes — are impaired.

[1]  G. Griffiths,et al.  Degranulation plays an essential part in regulating cell surface expression of Fas ligand in T cells and natural killer cells , 1999, Nature Medicine.

[2]  B. Dickey,et al.  Rab3D, a small GTPase, is localized on mast cell secretory granules and translocates to the plasma membrane upon exocytosis. , 1999, American journal of respiratory cell and molecular biology.

[3]  I. Maridonneau-Parini,et al.  The src-family protein-tyrosine kinase p59hck is located on the secretory granules in human neutrophils and translocates towards the phagosome during cell activation. , 1995, The Biochemical journal.

[4]  H. Lodish,et al.  Diffuse vesicular distribution of Rab3D in the polarized neuroendocrine cell line AtT‐20 , 1995, FEBS letters.

[5]  George Bou-Gharios,et al.  The activation of resting lymphocytes is accompanied by the biogenesis of lysosomal organelles , 1990, European Journal of Immunology.

[6]  C. Fletcher,et al.  Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[7]  M. Sheetz,et al.  Lytic granules from cytotoxic T cells exhibit kinesin-dependent motility on microtubules in vitro. , 1993, Journal of cell science.

[8]  M. Zvelebil,et al.  Fas ligand is targeted to secretory lysosomes via a proline-rich domain in its cytoplasmic tail. , 2001, Journal of cell science.

[9]  M. Triggiani,et al.  Molecular and cellular biology of mast cells and basophils. , 1997, International archives of allergy and immunology.

[10]  T. Olson,et al.  Targeting specific proteins for lysosomal proteolysis. , 1991, Biomedica biochimica acta.

[11]  G. Langford Actin- and microtubule-dependent organelle motors: interrelationships between the two motility systems. , 1995, Current opinion in cell biology.

[12]  A. Fischer,et al.  Two genes are responsible for Griscelli syndrome at the same 15q21 locus. , 2000, Genomics.

[13]  T. Ludwig,et al.  Differential Sorting of Lysosomal Enzymes Out of the Regulated Secretory Pathway in Pancreatic β-Cells , 1997, The Journal of cell biology.

[14]  J. Sixma,et al.  Activated Platelets Release Two Types of Membrane Vesicles: Microvesicles by Surface Shedding and Exosomes Derived From Exocytosis of Multivesicular Bodies and -Granules , 1999 .

[15]  D. Jäger,et al.  Serological cloning of a melanocyte rab guanosine 5'-triphosphate-binding protein and a chromosome condensation protein from a melanoma complementary DNA library. , 2000, Cancer research.

[16]  Marino Zerial,et al.  Rab proteins as membrane organizers , 2001, Nature Reviews Molecular Cell Biology.

[17]  T. Yokota,et al.  Expression of the Fas ligand in cells of T cell lineage. , 1995, Journal of immunology.

[18]  S. Grinstein,et al.  Subcellular distribution of docking/fusion proteins in neutrophils, secretory cells with multiple exocytic compartments. , 1995, Journal of immunology.

[19]  H. Lütcke,et al.  Isolation of a murine cDNA clone encoding Rab19, a novel tissue-specific small GTPase. , 1995, Gene.

[20]  T. Südhof,et al.  A small GTP-binding protein dissociates from synaptic vesicles during exocytosis , 1991, Nature.

[21]  M. Adam,et al.  Electron microscopic evidence for externalization of the transferrin receptor in vesicular form in sheep reticulocytes , 1985, The Journal of cell biology.

[22]  D. Wilkinson,et al.  Molecular control of neural crest formation, migration and differentiation. , 2000, Current opinion in cell biology.

[23]  Laurence Zitvogel,et al.  Eradication of established murine tumors using a novel cell-free vaccine: dendritic cell derived exosomes , 1998, Nature Medicine.

[24]  L. Collinson,et al.  Rab27a Regulates the Peripheral Distribution of Melanosomes in Melanocytes , 2001, The Journal of cell biology.

[25]  P. Bork,et al.  Identification and mutation analysis of the complete gene for Chediak–Higashi syndrome , 1996, Nature Genetics.

[26]  L. Page,et al.  Secretory Lysosome Biogenesis in Cytotoxic T Lymphocytes from Normal and Chediak Higashi Syndrome Patients , 2000, Traffic.

[27]  T. Fujisawa,et al.  Regulation of Cell Surface Expression of CTLA-4 by Secretion of CTLA-4-Containing Lysosomes Upon Activation of CD4+ T Cells1 , 2000, The Journal of Immunology.

[28]  G. Joberty,et al.  Comparison of the Effects on Secretion in Chromaffin and PC12 Cells of Rab3 Family Members and Mutants , 1999, The Journal of Biological Chemistry.

[29]  Ira Mellman,et al.  Dendritic Cells Specialized and Regulated Antigen Processing Machines , 2001, Cell.

[30]  S. Israels,et al.  Platelet dense granules: structure, function and implications for haemostasis. , 1999, Thrombosis research.

[31]  L. Traub,et al.  The trans-Golgi network: a late secretory sorting station. , 1997, Current opinion in cell biology.

[32]  U. Gullberg,et al.  Biosynthesis, processing and sorting of neutrophil proteins: insight into neutrophil granule development , 1997, European journal of haematology.

[33]  J. Dice,et al.  A molecular chaperone complex at the lysosomal membrane is required for protein translocation. , 2001, Journal of cell science.

[34]  J. Kaplan,et al.  Analysis of the Lysosomal Storage Disease Chediak–Higashi Syndrome , 2000, Traffic.

[35]  Q. Wei,et al.  Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor. , 1997, Journal of cell science.

[36]  A. Zweifach,et al.  Role of calcium influx in cytotoxic T lymphocyte lytic granule exocytosis during target cell killing. , 2001, Immunity.

[37]  R. Steinman,et al.  Transport of peptide-MHC class II complexes in developing dendritic cells. , 2000, Science.

[38]  J. Bonifacino,et al.  Adaptor-related proteins. , 2001, Current opinion in cell biology.

[39]  Robert C. Wolpert,et al.  A Review of the , 1985 .

[40]  J. Nordlund The pigmentary system : physiology and pathophysiology , 1998 .

[41]  K. Baetz,et al.  Serial killing by cytotoxic T lymphocytes: T cell receptor triggers degranulation, re‐filling of the lytic granules and secretion of lytic proteins via a non‐granule pathway , 1995, European journal of immunology.

[42]  L. Machesky,et al.  Rab27a Is Required for Regulated Secretion in Cytotoxic T Lymphocytes , 2001, The Journal of cell biology.

[43]  Jacques Neefjes,et al.  The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors , 2001, Current Biology.

[44]  G. Raposo,et al.  Distinct Protein Sorting and Localization to Premelanosomes, Melanosomes, and Lysosomes in Pigmented Melanocytic Cells✪ , 2001, The Journal of cell biology.

[45]  S. Kornfeld Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors. , 1992, Annual review of biochemistry.

[46]  Ira Mellman,et al.  The Formation of Immunogenic Major Histocompatibility Complex Class II–Peptide Ligands in Lysosomal Compartments of Dendritic Cells Is Regulated by Inflammatory Stimuli , 2000, The Journal of experimental medicine.

[47]  J. Glickman,et al.  Mannose 6-phosphate-independent targeting of lysosomal enzymes in I- cell disease B lymphoblasts , 1993, The Journal of cell biology.

[48]  J. Wolchok,et al.  Melanocyte differentiation marker gp75, the brown locus protein, can be regulated independently of tyrosinase and pigmentation. , 1995, The Journal of investigative dermatology.

[49]  N. Kedersha,et al.  Characterization of GMP-17, a granule membrane protein that moves to the plasma membrane of natural killer cells following target cell recognition. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[50]  H. Geuze,et al.  Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments , 1991, Nature.

[51]  L. Huber,et al.  Biogenesis of phagolysosomes proceeds through a sequential series of interactions with the endocytic apparatus , 1994, The Journal of cell biology.

[52]  G. Kandala,et al.  PDZ Domain Protein GIPC Interacts with the Cytoplasmic Tail of Melanosomal Membrane Protein gp75 (Tyrosinase-related Protein-1)* , 2001, The Journal of Biological Chemistry.

[53]  H. Geuze,et al.  Selective Enrichment of Tetraspan Proteins on the Internal Vesicles of Multivesicular Endosomes and on Exosomes Secreted by Human B-lymphocytes* , 1998, The Journal of Biological Chemistry.

[54]  Richard H. Scheller,et al.  SNARE-mediated membrane fusion , 2001, Nature Reviews Molecular Cell Biology.

[55]  K. von Figura,et al.  A di‐leucine‐based motif in the cytoplasmic tail of LIMP‐II and tyrosinase mediates selective binding of AP‐3 , 1998, The EMBO journal.

[56]  W S Oetting,et al.  The tyrosinase gene and oculocutaneous albinism type 1 (OCA1): A model for understanding the molecular biology of melanin formation. , 2000, Pigment cell research.

[57]  Barbara J. Reaves,et al.  Dense core lysosomes can fuse with late endosomes and are re-formed from the resultant hybrid organelles. , 1997, Journal of cell science.

[58]  S. Kornfeld,et al.  Asparagine-linked Oligosaccharides Protect Lamp-1 and Lamp-2 from Intracellular Proteolysis* , 1999, The Journal of Biological Chemistry.

[59]  A. Cuervo,et al.  A Receptor for the Selective Uptake and Degradation of Proteins by Lysosomes , 1996, Science.

[60]  S. Kingsmore,et al.  Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouse. , 1997, Human molecular genetics.

[61]  D. Castle,et al.  Relocation of the t-SNARE SNAP-23 from Lamellipodia-like Cell Surface Projections Regulates Compound Exocytosis in Mast Cells , 1998, Cell.

[62]  A. Hasilik,et al.  Biosynthesis of lysosomal enzymes in fibroblasts. Synthesis as precursors of higher molecular weight. , 1980, The Journal of biological chemistry.

[63]  M. Linial,et al.  Ca2+-dependent exocytosis in mast cells is stimulated by the Ca2+ sensor, synaptotagmin I. , 1998, Journal of immunology.

[64]  V. Setaluri Sorting and targeting of melanosomal membrane proteins: signals, pathways, and mechanisms. , 2000, Pigment cell research.

[65]  N. Copeland,et al.  A mutation in Rab27a causes the vesicle transport defects observed in ashen mice. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[66]  J. Hammer,et al.  Functions of unconventional myosins. , 2000, Current opinion in cell biology.

[67]  F. Paumet,et al.  Involvement of the ras-like GTPase rab3d in RBL-2H3 mast cell exocytosis following stimulation via high affinity IgE receptors (Fc epsilonRI). , 1997, Journal of immunology.

[68]  N. Hirashima,et al.  Rat basophilic leukemia cells express syntaxin-3 and VAMP-7 in granule membranes. , 2000, Biochemical and biophysical research communications.

[69]  T. Galli,et al.  Soluble NSF Attachment Protein Receptors (SNAREs) in RBL-2H3 Mast Cells: Functional Role of Syntaxin 4 in Exocytosis and Identification of a Vesicle-Associated Membrane Protein 8-Containing Secretory Compartment1 , 2000, The Journal of Immunology.

[70]  E. Haddad,et al.  Defective Granule Exocytosis in Rab27a-Deficient Lymphocytes from Ashen Mice , 2001, The Journal of cell biology.

[71]  G. Scott,et al.  Rab3a and SNARE proteins: potential regulators of melanosome movement. , 2001, The Journal of investigative dermatology.

[72]  R. Sagi-Eisenberg,et al.  Synaptotagmin II Negatively Regulates Ca2+-triggered Exocytosis of Lysosomes in Mast Cells , 1999, The Journal of experimental medicine.

[73]  J. Slot,et al.  Cytotoxic T lymphocyte granules are secretory lysosomes, containing both perforin and granzymes , 1991, The Journal of experimental medicine.

[74]  B. Storrie,et al.  The biogenesis of lysosomes: Is it a kiss and run, continuous fusion and fission process? , 1996, BioEssays : news and reviews in molecular, cellular and developmental biology.

[75]  Peter J. Peters,et al.  Molecules relevant for T cell‐target cell interaction are present in cytolytic granules of human T lymphocytes , 1989, European journal of immunology.

[76]  N. Andrews,et al.  Regulated secretion of conventional lysosomes. , 2000, Trends in cell biology.

[77]  G. Griffiths,et al.  Normal and abnormal secretion by haemopoietic cells , 2001, Immunology.

[78]  M. Inouye,et al.  Identification of a novel myosin-Va mutation in an ataxic mutant rat, dilute-opisthotonus , 2000, Mammalian Genome.

[79]  S. R. Terlecky,et al.  A role for a 70-kilodalton heat shock protein in lysosomal degradation of intracellular proteins. , 1989, Science.

[80]  P. Arvan,et al.  Mannose 6–Phosphate Receptors Are Sorted from Immature Secretory Granules via Adaptor Protein AP-1, Clathrin, and Syntaxin 6–positive Vesicles , 1998, The Journal of cell biology.

[81]  I. Martinez,et al.  Synaptotagmin VII Regulates Ca2+-Dependent Exocytosis of Lysosomes in Fibroblasts , 2000, The Journal of cell biology.

[82]  A. Chakraborty,et al.  Small Gtpase rab3A is associated with melanosomes in melanoma cells. , 2000, Pigment cell research.

[83]  A. Cuervo,et al.  Regulation of Lamp2a Levels in the Lysosomal Membrane , 2000, Traffic.

[84]  Q. Wei,et al.  Visualization of Melanosome Dynamics within Wild-Type and Dilute Melanocytes Suggests a Paradigm for Myosin V Function In Vivo , 1998, The Journal of cell biology.

[85]  L. Feng,et al.  Mouse models of Hermansky Pudlak syndrome: a review. , 1998, Pigment cell research.

[86]  C. Melief,et al.  B lymphocytes secrete antigen-presenting vesicles , 1996, The Journal of experimental medicine.

[87]  S. Orlow Melanosomes are specialized members of the lysosomal lineage of organelles. , 1995, The Journal of investigative dermatology.

[88]  A. Rudensky,et al.  Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells , 2001, The Journal of cell biology.

[89]  H. Horvitz,et al.  Caenorhabditis elegans rab-3 Mutant Synapses Exhibit Impaired Function and Are Partially Depleted of Vesicles , 1997, The Journal of Neuroscience.

[90]  J. Bonifacino,et al.  The molecular machinery for lysosome biogenesis * , 2001, BioEssays : news and reviews in molecular, cellular and developmental biology.

[91]  D. Ebert,et al.  Lysosomal enzyme secretory mutants of Dictyostelium discoideum. , 1990, Journal of cell science.

[92]  M. Marks,et al.  The melanosome: membrane dynamics in black and white , 2001, Nature Reviews Molecular Cell Biology.

[93]  J. Neefjes,et al.  Direct vesicular transport of MHC class II molecules from lysosomal structures to the cell surface , 1996, The Journal of cell biology.

[94]  A. Hasilik,et al.  Biosynthesis of lysosomal enzymes in fibroblasts. Phosphorylation of mannose residues. , 1980, The Journal of biological chemistry.

[95]  R. Baron,et al.  Cell-mediated extracellular acidification and bone resorption: evidence for a low pH in resorbing lacunae and localization of a 100-kD lysosomal membrane protein at the osteoclast ruffled border , 1985, The Journal of cell biology.

[96]  E. Caler,et al.  Plasma Membrane Repair Is Mediated by Ca2+-Regulated Exocytosis of Lysosomes , 2001, Cell.

[97]  S. Kingsmore,et al.  Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis. , 2000, Proceedings of the National Academy of Sciences of the United States of America.