Boron Supplementation Promotes Osteogenesis of Tibia by Regulating the Bone Morphogenetic Protein-2 Expression in African Ostrich Chicks

• Published in: Biological trace element research Vol. 199; no. 4; pp. 1544 - 1555
• Main Authors: Zhu, Daiyun, Ansari, Abdur Rahman, Xiao, Ke, Wang, Wei, Wang, Lei, Qiu, Weiwei, Zheng, Xinting, Song, Hui, Liu, Huazhen, Zhong, Juming, Peng, Kemei
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.04.2021; Springer Nature B.V
• Subjects: Apoptosis; Biochemistry; Biomedical and Life Sciences; Biomedical materials; Biotechnology; Bone morphogenetic protein 2; Bone morphogenetic proteins; Bones; Boron; Chicks; DNA nucleotidylexotransferase; Dosage; Drinking water; ELISA; Enzyme-linked immunosorbent assay; Glucocorticoids; Immunohistochemistry; Juveniles; Life Sciences; Nutrition; Oncology; Osteocalcin; Osteogenesis; Osteoprotegerin; Paraffin; Paraffins; Proteins; Receptors; Secretion; Serum; Staining; Supplements; Tibia; TRANCE protein; Boron; Histomorphometry; BMP-2; Ostrich chicks; Tibia osteogenesis
• ISSN: 0163-4984; 1559-0720
• DOI: 10.1007/s12011-020-02258-w

The present study aimed to explore the effects of supplemental boron on osteogenesis of tibia and to investigate the possible relationship between additional boron and the expression of bone morphogenetic protein-2 (BMP-2) in tibia of ostrich chicks. Therefore, forty-eight African ostrich chicks (15 days old) were supplemented with 0 mg/L, 40 mg/L, 80 mg/L, 160 mg/L, 320 mg/L, and 640 mg/L of boron in drinking water for 75 days. The paraffin sections of tibia used to measure histomorphometric parameters by hematoxylin and eosin (HE) staining, Masson’s staining, and immunohistochemistry (IHC). Enzyme-linked immunosorbent assay was performed to assess the level of BMP-2, osteocalcin (BGP), glucocorticoids (GCs), osteoprotegerin (OPG), and receptor activator of nuclear factor kappa-B ligand (RANKL) in serum. TUNEL (terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling) technique was performed to detect the cell apoptosis. The results indicated that low dose of supplemental boron (40 mg/L–160 mg/L) in drinking water promotes bone development by increasing the mature ossein. The expression of BMP2 on 45 days was higher than 90 days. Serum level of BMP-2, BGP, and GCs changed significantly in groups with low dosage of boron, and OPG/RANKL ratio was upregulated from 0 to 160 mg/L. Cell apoptosis was least in 40 mg/L and 160 mg/L groups. Taken together, low dose of boron supplemented in drinking water could promote osteogenesis and growth and development of tibia by regulating the expression and secretion of BMP-2 and providing a dynamically balanced environment for tibia growth, development, and reconstruction by regulating the concentrations of BGP, GCs, and OPG/RANKL ratio in serum.