3.8 Article

Phosphorylated Chitosan Hydrogels Inducing Osteogenic Differentiation of Osteoblasts via JNK and p38 Signaling Pathways

期刊

ACS BIOMATERIALS SCIENCE & ENGINEERING
卷 6, 期 3, 页码 1500-1509

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsbiomaterials.9b01374

关键词

phosphorous-containing hydrogels; osteogenic differentiation; MAPK signaling pathway

资金

  1. National Key Research and Development Program of China [2018YFA0703000]
  2. Science and Technology Program of Guangdong Province [2019B010941002, 2017B090911008, 2016A030306018]
  3. National Nature Science Foundation of China [U1801252, 51603074]
  4. Science and Technology Program of Guangzhou [201804020060]
  5. Outstanding Scholar Program of Guangzhou Regenerative Medicine and Health Guangdong Laboratory [2018GZR110102001]
  6. Shenzhen Science and Technology Program [JCYJ20170815153105076, GJHZ20180411143347603]

向作者/读者索取更多资源

Phosphorous-containing biopolymers have been applied to expedite the regeneration of damaged bone tissue by stimulating the function of phosphorous groups in natural bones. However, the underlying mechanism of phosphorous-containing biopolymers in promoting osteogenic differentiation is unclarified. Herein, we synthesized phosphorylated chitosan hydrogels by incorporating phosphocreatine into chitosan molecular chains under mild conditions. The introduction of phosphate groups improved properties of protein adsorption and calcium deposition without affecting the morphology of hydrogels. Our results showed that phosphorylated chitosan hydrogels could not only promote alkaline phosphatase activity and mineralization but also upregulate the expression of osteogenic-related genes and proteins. Meanwhile, application of c-Jun N-terminal kinase inhibitor SP600125 and p38 mitogen-activated protein kinase inhibitor SB203580 repressed the expression of osteogenic-related markers in gene and protein levels. To the best of our knowledge, it is reported for the first time that phosphorous-containing biopolymers promote osteogenic differentiation of osteoblasts via JNK and p38 signaling pathways.

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