TY - JOUR
T1 - Isolation of mitochondria, lysosomes, and microsomes from the rat ventral prostate with a note on inverted microsomal vesicles
AU - Haaparanta, Tapio
AU - Gustafsson, Jan Åke
AU - Glaumann, Hans
N1 - Funding Information:
This research was aided by the Swedish Cancer Society. The authors want to thank Mrs. Helena Jansson, Mrs. Annika Jubner, and Mrs. Ingrid Jons-son for valuable assistance.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1983/6
Y1 - 1983/6
N2 - A procedure is presented for the isolation of lysosomes, mitochondria, and microsomes from the rat ventral prostate with relatively good yield. Homogenization was performed with a Polytron homogenizer or in combination with the Potter-Elvehjem device. Reasonably pure mitochondria and lysosomes could only be obtained using a Metrizamide gradient, whereas it was possible to prepare pure microsomal fractions by differential centrifugation in sucrose. The purity of the lysosomes and mitochondria was 90 and 85%, respectively, as judged by the presence of different marker enzymes. These findings were confirmed by ultrastructural analyses. Electron micrographs of the isolated lysosomes showed intact lysosomes surrounded by a single membrane. The lysosomes contained intramatrical vesicles with lipid-like material. Vesicles derived from the endoplasmic reticulum in the microsomal fraction ranged from 70 to 90% depending on the centrifugal force used to sediment the mitochondrial fraction. Electron micrographs of the microsomal fraction showed that about 40% of the vesicles were inverted and turned "inside-out", i.e., having their ribosomes attached to the inside of the vesicles. By fractionation of ethylenediaminetetraacetate treated microsomes on a sucrose gradient a partially purified fraction was isolated which consisted of 65% of inverted microsomes.
AB - A procedure is presented for the isolation of lysosomes, mitochondria, and microsomes from the rat ventral prostate with relatively good yield. Homogenization was performed with a Polytron homogenizer or in combination with the Potter-Elvehjem device. Reasonably pure mitochondria and lysosomes could only be obtained using a Metrizamide gradient, whereas it was possible to prepare pure microsomal fractions by differential centrifugation in sucrose. The purity of the lysosomes and mitochondria was 90 and 85%, respectively, as judged by the presence of different marker enzymes. These findings were confirmed by ultrastructural analyses. Electron micrographs of the isolated lysosomes showed intact lysosomes surrounded by a single membrane. The lysosomes contained intramatrical vesicles with lipid-like material. Vesicles derived from the endoplasmic reticulum in the microsomal fraction ranged from 70 to 90% depending on the centrifugal force used to sediment the mitochondrial fraction. Electron micrographs of the microsomal fraction showed that about 40% of the vesicles were inverted and turned "inside-out", i.e., having their ribosomes attached to the inside of the vesicles. By fractionation of ethylenediaminetetraacetate treated microsomes on a sucrose gradient a partially purified fraction was isolated which consisted of 65% of inverted microsomes.
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U2 - 10.1016/0003-9861(83)90610-0
DO - 10.1016/0003-9861(83)90610-0
M3 - Article
C2 - 6859872
AN - SCOPUS:0020775408
SN - 0003-9861
VL - 223
SP - 458
EP - 467
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
IS - 2
ER -