Cellular localization and hormonal regulation of inducible nitric oxide synthase in cycling mouse uterus

• Published in: Journal of leukocyte biology 1995-01, Vol.57 (1), p.27-35
• Main Authors: Huang, Jian, Roby, Katherine F., Pace, Judith L., Russell, Stephen W., Hunt, Joan S.
• Format: Article
• Language: English
• Subjects: Amino Acid Oxidoreductases - analysis; Amino Acid Oxidoreductases - biosynthesis; Animals; Blotting, Western; Endometrium - cytology; Endometrium - enzymology; Enzyme Induction - drug effects; Estradiol - pharmacology; estrogen; Estrus - physiology; Female; Histocytochemistry; inducible nitric oxide synthase; macrophage; Macrophages - cytology; Macrophages - enzymology; mast cell; Mast Cells - cytology; Mast Cells - enzymology; Mice; mouse; Myometrium - cytology; Myometrium - enzymology; NADPH Dehydrogenase - analysis; Nitric Oxide Synthase; progesterone; Progesterone - pharmacology; uterus; Uterus - cytology; Uterus - enzymology; Uterus - physiology
• ISSN: 0741-5400; 1938-3673
• DOI: 10.1002/jlb.57.1.27

Nitric oxide (NO), a potent and versatile free radical, is synthesized in macrophages and mast cells as well as in other types of cells by the inducible form of nitric oxide synthase (iNOS). In this study, cells containing iNOS were identified in the uteri of cycling mice by using a rabbit antibody generated to an iNOS‐specific peptide. Macrophages were identified in semiserial sections of the same tissues with the monoclonal antibody, F4/80, and mast cells were identified by toluidine blue staining. In tissue sections of uteri obtained from mice in the four stages of the estrous cycle (8 to 11 mice per stage), iNOS immunoreactivity was strongest in diestrus‐I uteri and weakest in diestrus‐II uteri. Myometrial mast cells and endometrial epithelial cells were prominent locations of iNOS, and specific protein was also present in myometrial smooth muscle and macrophage‐like cells in the endometrial stroma. Because cyclic variations suggested regulation of iNOS expression by ovarian steroid hormones, studies were done using ovariectomized mice. Seven days after ovariectomy, immunoreactive iNOS was low but detectable in mast cells and luminal epithelial cells. In the uteri of ovariectomized, estradiol‐17β (E2)–treated mice, mast cells were iNOS+ after 24 h whereas epithelial cells were negative; the reverse was observed in progesterone (P4)‐treated mice. Both mast cells and epithelial cells were iNOS+ in the uteri of mice that had received a combination of E2 + P4. These results indicate that several types of uterine cells produce iNOS and that expression of this enzyme in specific cell lineages is governed by ovarian steroid hormones. The data are consistent with the postulate that NO derived from uterine leukocytes and other types of cells plays a role in uterine cyclicity and preparation for pregnancy. J. Leukoc. Biol. 57: 27–35; 1995.