Wood R L, Legg P G
J Cell Biol. 1970 Jun;45(3):576-85. doi: 10.1083/jcb.45.3.576.
The in vivo effects of 3-amino-1,2,4-triazole (AT) on the fine structure of microbodies in hepatic cells of male rats has been studied by the peroxidase-staining technique. Within 1 hr of intraperitoneal injection AT abolishes microbody peroxidase-staining, and the return of staining coincides temporally with the known pattern of return of catalase activity following AT inhibition; this is further evidence that the peroxidase staining of microbodies is due to catalase activity. Peroxidase staining reappears in the microbody matrix without evidence of either massive degradation or rapid proliferation of the organelles. Furthermore, during the period of return of activity, ribosomal staining occurs adjacent to microbodies whose matrix shows little or no peroxidase staining. These observations are interpreted as evidence that (a) catalase is capable of entering preexisting microbodies without traversing the cisternae of the rough endoplasmic reticulum or the Golgi apparatus, and that (b) the ribosomal staining is probably not cytochemical diffusion artifact and may represent a localized site of synthesis or activation of catalase.
采用过氧化物酶染色技术,研究了3-氨基-1,2,4-三唑(AT)对雄性大鼠肝细胞微体精细结构的体内效应。腹腔注射AT后1小时内,微体过氧化物酶染色消失,染色恢复与AT抑制后过氧化氢酶活性恢复的已知模式在时间上一致;这进一步证明微体的过氧化物酶染色是由于过氧化氢酶活性所致。过氧化物酶染色在微体基质中重新出现,没有细胞器大量降解或快速增殖的迹象。此外,在活性恢复期间,核糖体染色出现在微体附近,而微体基质的过氧化物酶染色很少或没有。这些观察结果被解释为以下证据:(a)过氧化氢酶能够进入预先存在的微体,而无需穿过粗面内质网或高尔基体的潴泡;(b)核糖体染色可能不是细胞化学扩散假象,可能代表过氧化氢酶合成或激活的局部位点。