Impairment of sterol biosynthesis leads to phosphorus and calcium accumulation in Leishmania acidocalcisomes

被引:36
作者
Vannier-Santos, MA
Martiny, A
Lins, U
Urbina, JA
Borges, VM
de Souza, W
机构
[1] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Programa Biol Celular & Parasitol, Lab Biol Celular Parasitaria, BR-21949900 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo de Goes, Setor Microscopia Eletr, BR-21941 Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Inst Microbiol Prof Paulo de Goes, Dept Microbiol Geral, BR-21941 Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, Lab Ultraestrutura Celular, BR-21941 Rio De Janeiro, Brazil
来源
MICROBIOLOGY-UK | 1999年 / 145卷
关键词
sterol biosynthesis inhibitors; ketoconazole; terbinafine; acidocalcisome; Leishmania;
D O I
10.1099/00221287-145-11-3213
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The induction of the formation of inclusion vesicles in Leishmania amazonensis by the sterol biosynthesis inhibitors (SBI) ketoconazole and terbinafine has been reported previously. These compartments were recently identified as acidocalcisomes. By the use of electron spectroscopic imaging and energy loss spectroscopy, the presence of calcium, phosphorus and oxygen in the electron-dense inclusions located within the acidocalcisomes has been demonstrated. Endoplasmic reticulum cisternae formed membrane whorls which enclosed large portions of the cytoplasm and sometimes circumscribed acidocalcisomes. In addition, acid phosphatase activity, as well as the endocytic tracers horseradish peroxidase and gold-labelled transferrin and cystatin C were detected within these organelles in both SBI-treated and untreated parasites. These data suggest that impairment of sterol biosynthesis induces the biogenesis of acidocalcisomes and triggers an autophagic process that leads to intersection of the endosomal/lysosomal system with the acidocalcisomes.
引用
收藏
页码:3213 / 3220
页数:8
相关论文
共 51 条
[11]  
Dunn William A. Jr., 1994, Trends in Cell Biology, V4, P139, DOI 10.1016/0962-8924(94)90069-8
[12]  
DVORAK JA, 1988, MOL BIOCHEM PARASIT, V31, P14
[13]  
GRAB DJ, 1992, EUR J CELL BIOL, V59, P398
[14]   EARLY STAGES OF ABSORPTION OF INJECTED HORSERADISH PEROXIDASE IN PROXIMAL TUBULES OF MOUSE KIDNEY - ULTRASTRUCTURAL CYTOCHEMISTRY BY A NEW TECHNIQUE [J].
GRAHAM, RC ;
KARNOVSKY, MJ .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1966, 14 (04) :291-+
[15]   Emerging targets for the development of novel antifungal therapeutics [J].
Groll, AH ;
De Lucca, AJ ;
Walsh, TJ .
TRENDS IN MICROBIOLOGY, 1998, 6 (03) :117-124
[16]   The lysosomal compartment as intracellular calcium store in MDCK cells: A possible involvement in InsP(3)-mediated Ca2+ release [J].
Haller, T ;
Dietl, P ;
Deetjen, P ;
Volkl, H .
CELL CALCIUM, 1996, 19 (02) :157-165
[18]   CYTOCHEMISTRY OF IN VITRO CULTURED TRYPANOSOMA THEILERI [J].
HERBERT, IV .
EXPERIMENTAL PARASITOLOGY, 1965, 16 (03) :348-&
[19]   FINE-STRUCTURE OF TRYPANOSOMA-CYCLOPS IN NONCELLULAR CULTURES [J].
HEYWOOD, P ;
WEINMAN, D ;
LIPMAN, M .
JOURNAL OF PROTOZOOLOGY, 1974, 21 (02) :232-238
[20]   DIFFERENTIATION OF HERPETOMONAS-MEGASELIAE - ULTRASTRUCTURAL OBSERVATIONS [J].
JANOVY, J ;
LEE, KW ;
BRUMBAUGH, JA .
JOURNAL OF PROTOZOOLOGY, 1974, 21 (01) :53-59