Journal of Biomedical Materials Research Part A, Volume 109, Issue 7, Pages 1113-1124 , 01/07/2021

Natural compounds from Leea macrophylla enhance phagocytosis and promote osteoblasts differentiation by alkaline phosphatase, type 1 collagen, and osteocalcin gene expression

Sayema Raiyan, Md Atiar Rahman, Md Abdullah Al Mamun, Md Muzammal Haque Asim, Arwa Makki, Dina Hajjar, Walla Alelwani, Jitbanjong Tangpong, Bijo Mathew

Abstract

The current study investigated the immunomodulating and osteoblast differentiation potential of the natural compounds from Leea macrophylla (LMN). Immunomodulatory effects have been investigated by the phagocytosis of Candida albicans using polymorphonuclear neutrophil cells in the in vitro slide method. A bioactivity-guided fractionation technique was used to evaluate the stimulating effect of L. macrophylla methanol extract on osteoblast differentiation using mouse osteoblastic cells. A low dose of LMN was found to stimulate the phagocytic effect better than a higher dose. The natural compounds from L. macrophylla have significantly increased alkaline phosphatase (ALP) and osteocalcin activities. The LMN promoted the osteoblast differentiation through upregulation of ALP, osteocalcin, and type 1 collagen in a dose-dependent manner. These natural compounds also upregulated ALP, osteocalcin, and type 1 collagen gene expressions. The data suggest that LMN has potential anabolic sequel on bone formation and osteoblast differentiation.

Document Type

Article

Source Type

Journal

Keywords

immunomodulationosteoblast differentiationosteocalcinphagocytosis

ASJC Subject Area

Engineering : Biomedical EngineeringMaterials Science : BiomaterialsMaterials Science : Ceramics and CompositesMaterials Science : Metals and Alloys

Funding Agency

University of Chittagong


Bibliography


Raiyan, S., Rahman, M., Al Mamun, M., Asim, M., Makki, A., Hajjar, D., Alelwani, W., ... Mathew, B. (2021). Natural compounds from Leea macrophylla enhance phagocytosis and promote osteoblasts differentiation by alkaline phosphatase, type 1 collagen, and osteocalcin gene expression. Journal of Biomedical Materials Research Part A, 109(7) 1113-1124. doi:10.1002/jbm.a.37103

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