HUMAN HEPATIC MICROBODIES WITH CRYSTALLOID CORES
HUMAN HEPATIC MICROBODIES WITH CRYSTALLOID CORES
复制标题
具有晶体核心的人肝微生物
作者:
L. Biempica
Hepatic microbodies were first described in 1956 by Rouiller and Bernhard (1) and by Gansler and Rouiller (2). In the rat, they are round or oval bodies that are somewhat smaller than mitochondria. They are delimited by a unit membrane and possess a moderately dense matrix and a dense core or nucleoid with a distinctive crystalloid arrangement. Microbodies have been characterized biochemically in rat liver and kidney by de Duve and his colleagues (3, 4). Density gradient centrifugation of rat liver has yielded fractions with numerous microbodies and high levels of urate oxidase (uricase), D-amino acid oxidase, and L-a-hydroxy acid oxidase, oxidases that form hydrogen peroxide, and catalase, an enzyme that destroys hydrogen peroxide. Because hydrogen peroxide is either the product or substrate of these enzymes, the term "peroxisome" has recently been proposed for these particles (5). A preparation with an 80-fold purification of urate oxidase contains a great number of free crystalloid cores (4). These observations suggest that D-amino acid oxidase and catalase are present in the matr ix and that urate oxidase is present in the core. Ra t kidney microbodies have no detectable urate oxidase activity (3). I t is of interest that in published electron micrographs, as in our own studies, rat kidney microbodies have central densities but no crystalloid structures (see Fig. 10 in reference 6). Although fish, amphibia, and most mammals exhibit urate oxidase activity, primates (including man), birds, and most reptiles lack this enzyme. The absence of urate oxidase in human and chick liver is consistent with the absence of the nucleoid in specimens examined in the electron microscope (7). This report describes the presence of crystalloidcontaining microbodies in a biopsy specimen of human liver.