A Cytochrome P450 Immunochemically Related to P450c,d(P450I) Localized to the Smooth Microsomes and Inner Zone of the Guinea Pig Adrenal*
- 1 May 1989
- journal article
- research article
- Published by The Endocrine Society in Endocrinology
- Vol. 124 (5) , 2480-2493
- https://doi.org/10.1210/endo-124-5-2480
Abstract
In addition to their capacity for steroid synthesis, guinea pig adrenal microsomes have a well documented ability to metabolize foreign compounds. The capacity for metabolism of foreign compounds is localized to the smooth endoplasmic reticulum-filled cells of the inner zone. However, it has been clear whether they possess cytochrome P450(s) specific for this function, distinct from the two known steroid hydroxylases, P45021 and P45017.alpha.. Multiple prominent protein bands in the mol wt range of known cytochrome P450s are seen on sodium dodecyl sulfate gels of guinea pig adrenal microsomes. Most are more intense in smooth microsomes, where the concentration of cytochrome P450 is highest. However, one band (52K) appears unique to the smooth microsomes. This band is also characteristic of microsomes obtained from the inner zone. This protein and two others (54K and 50K) are concentrated in the membrane pellet after carbonate treatment of the microsomes, indicating that they are integral membrane proteins. All three decrease in intensity after treatment of the animals with spironolactone, a compound known to cause depletion of adrenal cytochrome P450s. On Western blots of microsomal proteins the 54K and 50K proteins react with antibodies specific for P45017.alpha. and P45021, respectively. The 52K protein, characteristic of the smooth microsomes and inner zone, does not react with anti P45021 or anti-P45017.alpha., but does react with polyclonal antibody raised against microsomal cytochrome P450s induced by methylcholanthrene in rat liver (P450c,d). These results suggest that there is at least one additional cytochrome P450 in adrenal microsomes which is immunochemically distinct from P45021 and P45017.alpha.. Its localization to the smooth microsomes and inner zone microsomes correlates with the high activity for ethylmorphine metabolism detected in these fractions. This suggests that this cytochrome P450, which is immunochemically related to members of the P450I subfamily, may be associated with the ability of guinea pig adrenal microsomes to metabolize foreign compounds.This publication has 35 references indexed in Scilit:
- Purification and Partial Characterization of Hepatic Microsomal Cytochrome P-450s from Phenobarbital-and 3-Methylcholanthrene-Treated Rats1The Journal of Biochemistry, 1979
- Physicochemical properties of reduced nicotinamide adenine dinucleotide phosphate-cytochrome P-450 reductase from bovine adrenocortical microsomesBiochimica et Biophysica Acta (BBA) - Protein Structure, 1979
- Studies on the destruction of adrenal and testicular cytochrome P-450 by spironolactone. Requirement for the 7alpha-thio group and evidence for the loss of the heme and apoproteins of cytochrome P-450.Journal of Biological Chemistry, 1979
- MATURATIONAL CHANGES IN ADRENAL XENOBIOTIC METABOLISM IN MALE AND FEMALE GUINEA-PIGS1979
- Relation of Canrenone to the Actions of Spironolactone on Adrenal Cytochrome P-450-Dependent Enzymes*Endocrinology, 1978
- The corpus luteum of the guinea pig. III. Cytochemical studies on the Golgi complex and GERL during normal postpartum regression of luteal cells, emphasizing the origin of lysosomes and autophagic vacuoles.The Journal of cell biology, 1978
- Differential control of adrenal drug and steroid metabolism in the guinea pigLife Sciences, 1977
- Analytical study of microsomes and isolated subcellular membranes from rat liver. VI. Electron microscope examination of microsomes for cytochrome b5 by means of a ferritin-labeled antibody.The Journal of cell biology, 1976
- An improved staining procedure for the detection of the peroxidase activity of cytochrome P-450 on sodium dodecyl sulfate polyacrylamide gelsAnalytical Biochemistry, 1976
- A Rapid Spectrophotometric Assay of Monoamine Oxidase Based on the Rate of Disappearance of KynuramineJournal of Biological Chemistry, 1960