Golgi-dependent transport of cholesterol to the Chlamydia trachomatis inclusion

被引:213
作者
Carabeo, RA [1 ]
Mead, DJ [1 ]
Hackstadt, T [1 ]
机构
[1] NIAID, Host Parasite Interact Sect, Intracellular Parasites Lab, NIH,Rocky Mt Labs, Hamilton, MT 59840 USA
关键词
D O I
10.1073/pnas.1131289100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cholesterol, a lipid not normally found in prokaryotes, was identified in purified Chlamydia trachomatis elementary bodies and in the chlamydial parasitophorous vacuole (inclusion) membrane of infected HeLa cells. Chlamydiae obtained eukaryotic host cell cholesterol both from de novo synthesis or low-density lipoprotein. Acquisition of either de novo-synthesized cholesterol or low-density lipoprotein-derived cholesterol was microtubule-dependent and brefeldin A-sensitive, indicating a requirement for the Golgi apparatus. Transport also required chlamydial protein synthesis, indicative of a pathogen-directed process. The cholesterol trafficking pathway appears to coincide with a previously characterized delivery of sphingomyelin to the inclusion in that similar pharmacological treatments inhibited transport of both sphingomyelin and cholesterol. These results support the hypothesis that sphingomyelin and cholesterol may be cotransported via a Golgi-dependent pathway and that the chlamydial inclusion receives cholesterol preferentially from a brefeldin A-sensitive pathway of cholesterol trafficking from the Golgi apparatus to the plasma membrane.
引用
收藏
页码:6771 / 6776
页数:6
相关论文
共 52 条
  • [1] BRADFUTE DL, 1992, J BIOL CHEM, V267, P18308
  • [2] BUTLER JD, 1992, J BIOL CHEM, V267, P23797
  • [3] Chlamydia pneumoniae and atherosclerosis:: Links to the disease process
    Byrne, GI
    Kalayoglu, MV
    [J]. AMERICAN HEART JOURNAL, 1999, 138 (05) : S488 - S490
  • [4] PURIFICATION AND PARTIAL CHARACTERIZATION OF THE MAJOR OUTER-MEMBRANE PROTEIN OF CHLAMYDIA-TRACHOMATIS
    CALDWELL, HD
    KROMHOUT, J
    SCHACHTER, J
    [J]. INFECTION AND IMMUNITY, 1981, 31 (03) : 1161 - 1176
  • [5] The Salmonella-containing vacuole is a major site of intracellular cholesterol accumulation and recruits the GPI-anchored protein CD55
    Catron, DM
    Sylvester, MD
    Lange, Y
    Kadekoppala, M
    Jones, BD
    Monack, DM
    Falkow, S
    Haldar, K
    [J]. CELLULAR MICROBIOLOGY, 2002, 4 (06) : 315 - 328
  • [6] Toxoplasma gondii exploits host low-density lipoprotein receptor-mediated endocytosis for cholesterol acquisition
    Coppens, I
    Sinai, AP
    Joiner, KA
    [J]. JOURNAL OF CELL BIOLOGY, 2000, 149 (01) : 167 - 180
  • [7] COXEY RA, 1993, J LIPID RES, V34, P1165
  • [8] DAHL NK, 1993, J BIOL CHEM, V268, P16979
  • [9] FOLCH J, 1957, J BIOL CHEM, V226, P497
  • [10] FUTERMAN AH, 1990, J BIOL CHEM, V265, P8650