K. Johkura et al., IMMUNOHISTOCHEMICAL LOCALIZATION OF PEROXISOMAL ENZYMES IN DEVELOPINGRAT-KIDNEY TISSUES, The Journal of histochemistry and cytochemistry, 46(10), 1998, pp. 1161-1173
We studied the developmental changes in the localization of peroxisome
-specific enzymes in rat kidney tissues from embryonic Day 16 to postn
atal Week 10 by immunoblot analysis and immunohistochemistry, using an
tibodies for the peroxisomal enzymes catalase, D-amino acid oxidase, L
-alpha-hydroxyacid oxidase (isozyme B), and enoyl-CoA hydratase/3-hydr
oxyacyl-CoA dehydrogenase bifunctional protein. Peroxisomal enzymes we
re detected in the neonatal kidney by immunoblot analysis and their am
ount increased with kidney development. By light microscopic immunohis
tochemistry, they were first localized in a few proximal tubules in th
e juxtamedullary cortex of 18-day embryos. The distribution of proxima
l tubules positive for them expanded towards the superficial cortex wi
th development. The full thickness of the cortex became positive for t
he staining by 14 days after birth. Peroxisomes could be detected by e
lectron microscopy in structurally immature proximal tubules in 18-day
embryos. Their size increased and the ultrastructure of subcompartmen
ts became clear with continuing development of proximal tubules. These
results show that peroxisomal enzymes appear in the immature proximal
tubules in the kidney of embryos and that the ultrastructure of the p
eroxisomes and localization of the peroxisomal enzymes develop along w
ith the maturation of proximal tubules and kidney tissues.