Lytic granules, secretory lysosomes and disease

被引:112
作者
Clark, R [1 ]
Griffiths, GM [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0952-7915(03)00113-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lytic granules harbour many of the dangerous apoptosis-inducing molecules of the immune system, including perforin, granzymes and Fas ligand. Safe transport, storage and release of these lytic components is vital. As a secretory lysosome, the lytic granule is able to accomplish these roles, as well as conferring the lysosomal functions of cytotoxic T lymphocytes and natural killer cells. Secretory lysosomes are common to many other haemopoietic cells and also melanocytes. Many of the proteins used in lysosomal secretion are found in both melanocytes and hemopoietic cells, and are dysfunctional in genetic diseases with defects in these proteins. The genetically heterogeneous Hermansky-Pudlak syndrome represents an excellent model for revealing proteins involved in secretory lysosome functioning. However, studies of this disease reveal differences between the various different types of secretory lysosomes, including lytic granules.
引用
收藏
页码:516 / 521
页数:6
相关论文
共 49 条
  • [31] A novel motor, KIF13A, transports mannose-6-phosphate receptor to plasma membrane through direct interaction with AP-1 complex
    Nakagawa, T
    Setou, M
    Seog, DH
    Ogasawara, K
    Dohmae, N
    Takio, K
    Hirokawa, N
    [J]. CELL, 2000, 103 (04) : 569 - 581
  • [32] CYTOTOXIC LYMPHOCYTE-T GRANULES ARE SECRETORY LYSOSOMES, CONTAINING BOTH PERFORIN AND GRANZYMES
    PETERS, PJ
    BORST, J
    OORSCHOT, V
    FUKUDA, M
    KRAHENBUHL, O
    TSCHOPP, J
    SLOT, JW
    GEUZE, HJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (05) : 1099 - 1109
  • [33] Cytotoxic cell granule-mediated apoptosis - Characterization of the macromolecular complex of granzyme B with serglycin
    Raja, SM
    Wang, BK
    Dantuluri, M
    Desai, UR
    Demeler, B
    Spiegel, K
    Metkar, SS
    Froelich, CJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) : 49523 - 49530
  • [34] Griscelli disease:: Genotype-phenotype correlation in an array of clinical heterogeneity
    Sanal, O
    Ersoy, F
    Tezcan, I
    Metin, A
    Yel, L
    Ménasché, G
    Gürgey, A
    Berkel, I
    de Saint Basile, G
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 2002, 22 (04) : 237 - 243
  • [35] The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome
    Starcevic, M
    Nazarian, R
    Dell'Angelica, EC
    [J]. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2002, 13 (04) : 271 - 278
  • [36] The immunological synapse of CTL contains a secretory domain and membrane bridges
    Stinchcombe, JC
    Bossi, G
    Booth, S
    Griffiths, GM
    [J]. IMMUNITY, 2001, 15 (05) : 751 - 761
  • [37] Rab27a is required for regulated secretion in cytotoxic T lymphocytes
    Stinchcombe, JC
    Barral, DC
    Mules, EH
    Booth, S
    Hume, AN
    Machesky, LM
    Seabra, MC
    Griffiths, GM
    [J]. JOURNAL OF CELL BIOLOGY, 2001, 152 (04) : 825 - 833
  • [38] Secretory lysosome biogenesis in cytotoxic T lymphocytes from normal and Chediak Higashi syndrome patients
    Stinchcombe, JC
    Page, LJ
    Griffiths, GM
    [J]. TRAFFIC, 2000, 1 (05) : 435 - 444
  • [39] Failure of trafficking and antigen presentation by CD1 in AP-3-deficient cells
    Sugita, M
    Cao, XC
    Watts, GFM
    Rogers, RA
    Bonifacino, JS
    Brenner, MB
    [J]. IMMUNITY, 2002, 16 (05) : 697 - 706
  • [40] Mouse models of Hermansky Pudlak Syndrome: A review
    Swank, RT
    Novak, EK
    McGarry, MP
    Rusiniak, ME
    Feng, LJ
    [J]. PIGMENT CELL RESEARCH, 1998, 11 (02): : 60 - 80