Litwin J A
Cell Tissue Res. 1984;238(3):635-42. doi: 10.1007/BF00219882.
Rat liver fixed by perfusion with low glutaraldehyde concentrations was incubated in diaminobenzidine-containing medium to stain for peroxidase. Endogenous peroxidatic activity was found not only in Kupffer cells but also in the endothelial cells lining the sinusoids and central veins. The reaction product was localized in the nuclear envelope and endoplasmic reticulum. The peroxidatic activity in endothelial cells showed a concentration-dependent sensitivity to glutaraldehyde: in liver samples fixed with 0.25% glutaraldehyde, approx. 23% of the sinusoidal endothelial cells and 65% of central vein endothelium were peroxidase-positive; with 0.5% glutaraldehyde, only approx. 8% of the sinusoidal endothelial cells contained detectable amounts of the reaction product; with 1.5% glutaraldehyde all endothelial cells were consistently peroxidase-negative. No peroxidatic activity could be found in liver endothelial cells following isolation by centrifugal elutriation. Endothelial cell peroxidase may possibly be involved in defense responses of liver and/or, as a part of prostaglandin synthase system, in prostanoid production.
用低浓度戊二醛灌注固定的大鼠肝脏,置于含二氨基联苯胺的培养基中孵育以进行过氧化物酶染色。发现内源性过氧化物酶活性不仅存在于枯否细胞中,也存在于肝血窦和中央静脉内衬的内皮细胞中。反应产物定位于核膜和内质网。内皮细胞中的过氧化物酶活性对戊二醛表现出浓度依赖性敏感性:在用0.25%戊二醛固定的肝脏样本中,约23%的肝血窦内皮细胞和65%的中央静脉内皮细胞过氧化物酶呈阳性;用0.5%戊二醛时,只有约8%的肝血窦内皮细胞含有可检测量的反应产物;用1.5%戊二醛时,所有内皮细胞始终过氧化物酶呈阴性。通过离心淘析分离后,在肝脏内皮细胞中未发现过氧化物酶活性。内皮细胞过氧化物酶可能参与肝脏的防御反应和/或作为前列腺素合酶系统的一部分参与前列腺素的产生。