Alendronate disturbs vesicular trafficking in osteoclasts

被引:74
作者
Alakangas, A
Selander, K
Mulari, M
Halleen, J
Lehenkari, P
Mönkkönen, J
Salo, J
Väänänen, K
机构
[1] Univ Turku, Inst Biomed, Dept Anat, FIN-20520 Turku, Finland
[2] Univ Oulu, Dept Surg, SF-90220 Oulu, Finland
[3] Univ Kuopio, Dept Pharmaceut, FIN-70211 Kuopio, Finland
[4] Univ Helsinki, Cent Hosp, Dept Orthopaed & Traumatol, SF-00260 Helsinki, Finland
关键词
alendronate; bone resorption; bisphosphonates; osteoclast; vesicle transport;
D O I
10.1007/s002230010047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The nitrogen-containing bisphosphonate alendronate inhibits osteoclast-mediated bone resorption through inhibition of the mevalonate pathway. This results in impaired protein prenylation and may affect the function of small GTPases in osteoclasts. Since these proteins are important regulators of vesicle transport in cells. we investigated the possible interference of alendronate with these processes in isolated rat osteoclasts. We show here that alendronate-induced inhibition of bone resorption coincides with accumulation of tartrate-resistant acid phosphatase- and electron dense material-containing tubular vesicles in osteoclasts. Alendronate-induced changes in osteoclasts also included widening of the sealing zone areas and incomplete organization of tight attachments and ruffled borders. Osteoclasts also appeared partially detached from the bone surface, and organic matrix was typically dissolved only at the edges of the resorption pits on alendronate-coated bone slices. In contrast, resorption pits on the control and clodronate-coated bone slices were thoroughly resorbed. Inhibition of bone resorption by alendronate was not. however, related to a decrease in osteoclast number. In conclusion, our findings suggest that alendronate inactivates osteoclasts by mechanisms that impair their intracellular vesicle transport, apoptosis being only a secondary phenomenon to this.
引用
收藏
页码:40 / 47
页数:8
相关论文
共 42 条
[31]   Bisphosphonates act directly on the osteoclast to induce caspase cleavage of Mst1 kinase during apoptosis - A link between inhibition of the mevalonate pathway and regulation of an apoptosis-promoting kinase [J].
Reszka, AA ;
Halasy-Nagy, JM ;
Masarachia, PJ ;
Rodan, GA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) :34967-34973
[32]   Bisphosphonates: From the laboratory to the clinic and back again [J].
Russell, RGG ;
Rogers, MJ .
BONE, 1999, 25 (01) :97-106
[33]   BISPHOSPHONATES ACT ON RAT BONE-RESORPTION THROUGH THE MEDIATION OF OSTEOBLASTS [J].
SAHNI, M ;
GUENTHER, HL ;
FLEISCH, H ;
COLLIN, P ;
MARTIN, TJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (05) :2004-2011
[34]   Removal of osteoclast bone resorption products by transcytosis [J].
Salo, J ;
Lehenkari, P ;
Mulari, M ;
Metsikko, K ;
Vaananen, HK .
SCIENCE, 1997, 276 (5310) :270-273
[35]   BISPHOSPHONATE ACTION - ALENDRONATE LOCALIZATION IN RAT BONE AND EFFECTS ON OSTEOCLAST ULTRASTRUCTURE [J].
SATO, M ;
GRASSER, W ;
ENDO, N ;
AKINS, R ;
SIMMONS, H ;
THOMPSON, DD ;
GOLUB, E ;
RODAN, GA .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (06) :2095-2105
[36]   Protein-tyrosine phosphatase activity regulates osteoclast formation and function: Inhibition by alendronate [J].
Schmidt, A ;
Rutledge, SJ ;
Endo, N ;
Opas, EE ;
Tanaka, H ;
Wesolowski, G ;
Leu, CT ;
Huang, Z ;
Ramachandaran, C ;
Rodan, SB ;
Rodan, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :3068-3073
[37]   THE EFFECTS OF BISPHOSPHONATES ON THE RESORPTION CYCLE OF ISOLATED OSTEOCLASTS [J].
SELANDER, K ;
LEHENKARI, P ;
VAANANEN, HK .
CALCIFIED TISSUE INTERNATIONAL, 1994, 55 (05) :368-375
[38]  
Selander KS, 1996, MOL PHARMACOL, V50, P1127
[39]  
Väänänen HK, 2000, J CELL SCI, V113, P377
[40]   The role of geranylgeranylation in bone resorption and its suppression by bisphosphonates in fetal bone explants in vitro:: A clue to the mechanism of action of nitrogen-containing bisphosphonates [J].
van Beek, E ;
Löwik, C ;
van der Pluijm, G ;
Papapoulos, S .
JOURNAL OF BONE AND MINERAL RESEARCH, 1999, 14 (05) :722-729