Application of in situ hybridization, cytochemical and immunocytochemical techniques for the investigation of peroxisomes - A review including novel data

被引:28
作者
Baumgart, E
机构
[1] Institute for Anatomy and Cell Biology,
[2] Department of Medical Cell Biology,undefined
[3] University of Heidelberg,undefined
[4] Im Neuenheimer Feld 307,undefined
[5] D-69120 Heidelberg,undefined
[6] Germany Tel. +49-6221-548662/548663; Fax +49–6221-544952; e-mail Baumgart@novsrv1.pio1.uni-heidelberg.de,undefined
关键词
D O I
10.1007/s004180050160
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In situ hybridization, cytochemical and immunocytochemical techniques have contributed significantly to the understanding of the biology of peroxisomes, since they permit in situ demonstration of the sites of synthesis and distribution of peroxisomal proteins without the necessity of homogenization and subcellular fractionation of tissues or cultured cells. This article reviews the results of research on mammalian peroxisomal metabolism, biogenesis and proliferation in which morphological techniques have played a significant role in the elucidation of the biological problem. Some new data on peroxisomal heterogeneity and morphogenesis are included. The morphological methods applied have made it possible to characterize the differences in distribution of mRNAs encoding peroxisomal proteins in different tissues, as well as to monitor the marked heterogeneity in the protein composition and in the activity of specific enzymes in the peroxisomal population of single cells, or in tissues with complex organization (e.g. liver and kidney). In addition, the dynamic alterations and high plasticity of the peroxisomal compartment - partly dependent on contact of the peroxisomes to the microtubular network - are presented.
引用
收藏
页码:185 / 210
页数:26
相关论文
共 154 条
[31]   Identification and characterization of the 2-enoyl-CoA hydratases involved in peroxisomal beta-oxidation in rat liver [J].
DieuaideNoubhani, M ;
Novikov, D ;
Vandekerckhove, J ;
VanVeldhoven, PP ;
Mannaerts, GP .
BIOCHEMICAL JOURNAL, 1997, 321 :253-259
[32]   Further characterization of the peroxisomal 3-hydroxyacyl-CoA dehydrogenases from rat liver - Relationship between the different dehydrogenases and evidence that fatty acids and the C-27 bile acids di- and tri-hydroxycoprostanic acids are metabolized by separate multifunctional proteins [J].
DieuaideNoubhani, M ;
Novikov, D ;
Baumgart, E ;
Vanhooren, JCT ;
Fransen, M ;
Goethals, M ;
Vandekerckhove, J ;
VanVeldhoven, PP ;
Mannaerts, GP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 240 (03) :660-666
[33]   Unified nomenclature for peroxisome biogenesis factors [J].
Distel, B ;
Erdmann, R ;
Gould, SJ ;
Blobel, G ;
Crane, DI ;
Cregg, JM ;
Dodt, G ;
Fujiki, Y ;
Goodman, JM ;
Just, WW ;
Kiel, JAKW ;
Kunau, WH ;
Lazarow, PB ;
Mannaerts, GP ;
Moser, HW ;
Osumi, T ;
Rachubinski, RA ;
Roscher, A ;
Subramani, S ;
Tabak, HF ;
Tsukamoto, T ;
Valle, D ;
vanderKlei, I ;
vanVeldhoven, PP ;
Veenhuis, M .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :1-3
[34]   CONTROL OF THE PEROXISOMAL BETA-OXIDATION PATHWAY BY A NOVEL FAMILY OF NUCLEAR HORMONE RECEPTORS [J].
DREYER, C ;
KREY, G ;
KELLER, H ;
GIVEL, F ;
HELFTENBEIN, G ;
WAHLI, W .
CELL, 1992, 68 (05) :879-887
[35]  
ELGERSMA Y, 1995, THESIS U AMSTERDAM
[36]   GIANT PEROXISOMES IN OLEIC ACID-INDUCED SACCHAROMYCES-CEREVISIAE LACKING THE PEROXISOMAL MEMBRANE-PROTEIN PMP27P [J].
ERDMANN, R ;
BLOBEL, G .
JOURNAL OF CELL BIOLOGY, 1995, 128 (04) :509-523
[37]  
ERDMANN R, 1997, IN PRESS TRENDS CELL
[38]  
ESPEEL M, 1995, EUR J CELL BIOL, V67, P319
[39]  
ESPEEL M, 1993, ULTRASTRUCT PATHOL, V17, P625
[40]  
Fahimi H.D., 1993, PEROXISOMES BIOL IMP, P395