Heme oxygenase isozymes in bone: induction of HO-1 mRNA following physiological levels of mechanical loading in vivo

• Published in: Bone (New York, N.Y.) N.Y.), 1998-11, Vol.23 (5), p.433-436
• Main Authors: Rawlinson, S.C.F., Zaman, G., Mosley, J.R., Pitsillides, A.A., Lanyon, L.E.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Blotting, Northern; DNA Primers - chemistry; Female; Heme oxygenase; Heme Oxygenase (Decyclizing) - biosynthesis; Heme Oxygenase (Decyclizing) - genetics; Heme Oxygenase-1; Immunoenzyme Techniques; Investigative techniques, diagnostic techniques (general aspects); Mechanical load; Medical sciences; Osteoarticular system. Muscles; Osteoblasts; Osteoblasts - metabolism; Osteocytes; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Rats; Rats, Sprague-Dawley; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - biosynthesis; Space life sciences; Stress, Mechanical; Ulna - cytology; Ulna - enzymology; Weight-Bearing - physiology
• ISSN: 8756-3282; 1873-2763
• DOI: 10.1016/S8756-3282(98)00125-2

Heme oxygenases (HO) are responsible for the production of carbon monoxide, which has been suggested to act similarly to nitric oxide as a signaling molecule. Inducible HO-1 and constitutive HO-2 were located in sections of weight-bearing ulnae of the rat by immunocytochemistry. Intense HO-1 localization was restricted to peri- and endosteal sites, whereas HO-2 staining occurred in osteoblasts and osteocytes throughout the cortex. Northern blot hybridization of mRNA levels for HO-1 and HO-2 extracted from bones was also performed. Six hours after a single 10 min period of noninvasive mechanical loading of the ulna in vivo, generating physiological levels of strain sufficient to initiate an osteogenic response, the level of mRNA for the inducible HO-1 isoform was increased, but that of HO-2 was unchanged. The presence of a constitutive and strain-related upregulation of an inducible enzyme capable of producing carbon monoxide suggests that carbon monoxide may participate not only in bone cells’ basal metabolism but also in their adaptive responses to mechanical load.