Synergistic Osteogenic and Antiapoptotic Framework Nucleic Acid Complexes Prevent Diabetic Osteoporosis

Author:

Bai Long123,Feng Maogeng4,Zhang Qiuwen2,Cai Zhengwen3,Li Qiumei2,Li Yong23,Ma Chuan12,Xiao Jingang12,Lin Yunfeng3ORCID

Affiliation:

1. Department of Oral Implantology The Affiliated Stomatological Hospital Southwest Medical University Luzhou 646000 P. R. China

2. Luzhou Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration Luzhou 646000 P. R. China

3. State Key Laboratory of Oral Diseases National Center for Stomatology National Clinical Research Center for Oral Diseases West China Hospital of Stomatology Sichuan University Chengdu Sichuan 610041 P. R. China

4. Department of Oral and Maxillofacial Surgery Dazhou Central Hospital Dazhou 635000 P. R. China

Abstract

AbstractDiabetes mellitus (DM) is characterized by elevated blood glucose and advanced glycation end product (AGEs) levels. Increased AGEs in bone tissue inhibit osteogenic differentiation by bone marrow mesenchymal stem cells (BMSCs), leading to bone loss and osteoporosis in diabetic patients. Enhancing the osteogenic differentiation capacity of BMSCs in the presence of abundant AGEs can improve bone health and prevent osteoporosis in DM patients. The flavonoid, Quercetin, has anti‐inflammatory, antibacterial, and antitumor properties; however, it is insoluble in water and thus not easily absorbed by the body. Nanodrug delivery systems such as tetrahedral framework nucleic acids (tFNAs) exhibit excellent biocompatibility, efficient cell uptake, and drug piggybacking. In the present study, tFNAs with quercetin is complexed to form a novel nanodrug (tFNAs/Que) that combined the features of both components. tFNAs/Que promote osteogenic differentiation by BMSCs in an in vitro AGEs‐rich environment, maintain bone mass, and prevent diabetic osteoporosis in DM mice in vivo. The mechanism of tFNAs/Que against AGEs may be related to the JNK signaling pathway. In conclusion, it is shown that tFNAs/Que has a dual regulatory role by promoting osteogenic differentiation and inhibiting apoptosis. Such a feature is promising for the prevention and treatment of diabetic osteoporosis.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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