CHANGES OF COLON EPITHELIUM PROLIFERATION DUE TO INDIVIDUAL AGING WITH CYCLIN PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA CYCLIN) IMMUNOSTAINING COMPARED TO [H-3] THYMIDINE AUTORADIOGRAPHY
T. Morita et al., CHANGES OF COLON EPITHELIUM PROLIFERATION DUE TO INDIVIDUAL AGING WITH CYCLIN PROLIFERATING CELL NUCLEAR ANTIGEN (PCNA CYCLIN) IMMUNOSTAINING COMPARED TO [H-3] THYMIDINE AUTORADIOGRAPHY, Histochemistry, 101(1), 1994, pp. 13-20
We report a change in the proliferative activity of mouse colonic epit
helium due to development and aging. In order to measure the prolifera
tive activity, colonic epithelium was immunostained for cyclin prolife
rating cell nuclear antigen (PCNA/cyclin), which appears from the GI t
o the S phase of the cell cycle, and compared with labeling obtained b
y [H-3]-thymidine radioautography. Litter mice of six age groups from
the fetal period (embryonic day 19), newborn period (postnatal day 1),
suckling period (postnatal day 5), weaning period (postnatal dy 21),
adult period (2 month old) to the senescent period (11 month old) were
examined by immunohistochemistry. The descending colons were fixed in
methacarn (method-Carnoy) and embedded in paraffin. Sections were sta
ined for PCNA/cyclin activity using 19A2 monoclonal antibody and the a
vidin-biotin peroxidase complex (ABC) technique. For radioautography,
litter mice of nine age groups using in vivo intraperitoneal administr
ation of [H-3]-thymidine. The labeling indices of colonic epithelial c
ells in the proliferative zone were then analyzed and compared between
the two investigative methods. Our results show that the proliferativ
e activity of mice colon was high in the fetal and newborn periods and
almost constant from the suckling period to senescence, as demonstrat
ed by both PCNA/cyclin immunohistochemistry and [H-3]thymidine radioau
tography. The labeling index seen by PCNA/cyclin immunohistochemistry
was, however, higher than that seen by [H-3]-thymidine radioautography
.