Differentiation of liver peroxisomes in the foetal and newborn rat. Cytochemistry of catalase and D-aminoacid oxidase

Development ◽  
1985 ◽  
Vol 88 (1) ◽  
pp. 151-163
Author(s):  
S. Stefanini ◽  
M. G. Farrace ◽  
M. P. Cerù Argento

Organules containing cytochemically detectable amounts of catalase and D-aminoacid oxidase activities are observed between the 14th and 21st day of development in the parenchymal cells of the foetal rat liver and in the liver of newborn rats. As early as 14 to 15 days, a limited number of small microperoxisomes, scattered in the cytoplasm of very few hepatocytes, can be found. These are roundish shaped, have a granulous matrix and contain very low, hardly detectable levels of the above mentioned enzymes. In later development both the size and the enzymatic content of the organules gradually increase, approaching adult levels at the end of foetal development. Starting from the 18th to 19th day of intrauterine life nucleoids can be seen in many peroxisomes. The morphological and biochemical maturation from microperoxisomes to peroxisomes is accompanied by a gradual increase in the number of stainable organules, both per individual cell and per tissue area.

1984 ◽  
Vol 222 (3) ◽  
pp. 837-838 ◽  
Author(s):  
M Van Dijk ◽  
P Lund

N-Acetylglutamate is present in foetal rat liver at 17 days' gestation. The tissue content (approx. 50 nmol/g wet wt.) remains constant during later foetal life. The appearance of N-acetylglutamate does not parallel the developmental pattern of the urea cycle.


1993 ◽  
Vol 71 (3-4) ◽  
pp. 133-140 ◽  
Author(s):  
Hing Man Chan ◽  
M. George Cherian

The relative quantities of the two metallothionein isoforms (MT-1 and MT-2) in prenatal and newborn rat livers have been quantified using a competitive enzyme-linked immunosorbent assay with two specific polyclonal antisera. Both MT isoforms were detected in fetal liver on gestation day 16 and their levels continued to increase into the neonatal period. A concomitant increase was observed in plasma MT levels in the pregnant rats. The level of MT-2 was higher (75%) than that of MT-1 in the liver of both prenatal and neonatal rats. Both hepatic MT isoforms showed a significant correlation (P < 0.05) with the hepatic Zn level. Immunohistochemical localization of MT isoforms showed no apparent difference in intracellular distribution. Both MT isoforms were mainly cytoplasmic in fetal rat liver. Intense intranuclear staining was observed in newborn rat liver when the total MT concentration reached a maximum of over 1 mg MT/g tissue. The nuclear MT staining decreased with age, and at day 7, approximately equal concentrations of MT were found in nucleus and cytoplasm. When the newborn rats (1 day old) were injected with Zn (10 mg/kg), both MT isoforms were induced on days 2 and 7. Injection of Cd (1 mg/kg) increased the hepatic MT levels only on day 7. The level of MT-2 remained higher than that of MT-1 in all cases. These results suggest that both MT isoforms play a similar role in the metabolism of Zn during early development and the relative abundance of the MT isoforms may be a species-specific phenomenon.Key words: ontogeny, metallothionein, isoforms, immunohistochemistry, metals.


1976 ◽  
Vol 251 (10) ◽  
pp. 3014-3020 ◽  
Author(s):  
R F Kletzien ◽  
M W Pariza ◽  
J E Becker ◽  
V R Potter ◽  
F R Butcher

1987 ◽  
Vol 262 (36) ◽  
pp. 17420-17425 ◽  
Author(s):  
S L Thompson ◽  
R Burrows ◽  
R J Laub ◽  
S K Krisans

1994 ◽  
Vol 269 (43) ◽  
pp. 27125-27135
Author(s):  
D K Novikov ◽  
G F Vanhove ◽  
H Carchon ◽  
S Asselberghs ◽  
H J Eyssen ◽  
...  

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