S. Awasthi et al., RAT GST-8-8 IS EXPRESSED PREDOMINANTLY IN MYELOID ORIGIN CELLS INFILTRATING THE GRAVID UTERUS, International journal of biochemistry & cell biology, 29(5), 1997, pp. 807-813
Previous studies from our laboratory have shown a relatively high expr
ession of rGST8-8 in uterine tissues. This GST isozyme displays relati
vely high glutathione-peroxidase activity towards lipid-hydroperoxides
and towards toxic 4-hydroxyalkenals generated from lipid peroxidation
. Since the uterus is a unique organ, subject to oxidative stress due
to infiltration by immune effector cells during gestation and because
this infiltration is readily identifiable histologically, the studies
reported herein were performed to localize the cell specific expressio
n of rGST8-8 to determine whether immune effector cells infiltrating t
he pregnant rat uterus specifically expressed rGST8-8. A 75 bp end-rad
iolabeled cRNA probe was prepared from the full length mGSTA4-4 cDNA f
rom the region which is highly homologous with rGST8-8. This cRNA prob
e was used for in situ hybridization studies to localize rGST8-8 in sp
ecific cell types of gravid rat uterus. Results of these studies indic
ate that this GST isozyme is selectively expressed in myeloid origin c
ells such as monocytes/macrophages, and neutrophils infiltrating the u
terine endometrium and in vascular walls. Selective expression of rGST
8-8 in the myeloid origin cells, which are known to generate higher le
vels of reactive oxygen species, suggests that this GST isozyme plays
an important role in the protection mechanisms against lipid peroxidat
ion. (C) 1997 Elsevier Science Ltd.