Novel Sites of Adrenomedullin Gene Expression in Mouse and Rat Tissues

• Published in: Endocrinology (Philadelphia) 1998-05, Vol.139 (5), p.2253-2264
• Main Authors: Cameron, Vicky A., Fleming, Angela M.
• Format: Article
• Language: English
• Subjects: Adrenal Glands - chemistry; Adrenal medulla; Adrenomedullin; Adrenomedullin gene; Alveoli; Animal tissues; Animals; Antimicrobial agents; Atria; Corpus luteum; Digestive System - chemistry; Distal tubules; DNA probes; Endometrium; Epithelial cells; Epithelial Cells - chemistry; Epithelium; Female; Females; Follicles; Gastrointestinal system; Gastrointestinal tract; Gene Expression; Genitalia - chemistry; Glomerulus; Hepatocytes; Hybridization; In Situ Hybridization; Intestine; Kidney - chemistry; Localization; Lung - chemistry; Male; Mice; Mice, Inbred BALB C; Molecular Sequence Data; Myocardium - chemistry; Peptides; Peptides - genetics; Pheochromocytoma; Pituitary (anterior); Pituitary (posterior); Pituitary Gland - chemistry; Probes; Rats; Rats, Sprague-Dawley; RNA probes; RNA, Messenger - analysis; Skeletal muscle; Small intestine; Submandibular gland; Uterus
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/endo.139.5.5965

Abstract Adrenomedullin (AM) was originally identified in pheochromocytoma tissue and was characterized as a hypotensive peptide. The tissue distribution and cellular localization of AM messenger RNA (mRNA) were determined in mouse and rat tissues by in situ hybridization. Three probes were used: two nonoverlapping probes to the pro-AM N-terminal 20 peptide (PAMP) and AM peptide regions of mouse pro-AM, and a larger complementary DNA (cDNA) probe spanning both the PAMP- and AM peptide-coding regions. The most intense expression of AM mRNA was in endometrium and epithelial cells lining the uterus and mouse adrenal medulla. Moderate levels of expression were detected in kidney glomerulus and cortical distal tubules, ovarian corpus luteum and follicles, epithelial cells lining the bronchioles, cardiac atrium and ventricle, posterior pituitary (particularly in female rats), stomach, small intestine (microvilli, mucosa and submucosa), spleen, and pancreas. Lower levels were observed in pulmonary alveoli, anterior pituitary, and submandibular gland. No expression was detected in the testis, thymus, skeletal muscle, or liver. The localization of AM mRNA in epithelial cells lining the uterus, bronchioles, and gastrointestinal tract indicates novel roles for AM, possibly as an antimicrobial agent. The strong expression of AM in uterus, ovary, and posterior pituitary suggests that AM plays a role in female reproduction.