Preparation and characterization of a novel triple composite scaffold containing silk fibroin, chitosan, extracellular matrix and the mechanism of Akt/FoxO signaling pathway in colonic cancer cells cultured in 3D

被引:1
|
作者
Cao, Zhipeng [1 ]
Chen, Liang [1 ]
Niu, Gengming [1 ]
Li, Yan [1 ]
Hu, Zhiqing [1 ]
Hong, Runqi [1 ]
Zhang, Xiaotian [1 ]
Hong, Liang [1 ]
Han, Shanliang [1 ]
Ke, Chongwei [1 ]
机构
[1] Fudan Univ, Peoples Hosp Shanghai 5, Dept Gen Surg, Shanghai, Peoples R China
关键词
extracellular matrix; silk fibroin; chitosan; scaffolds; Akt; FoxO signaling pathway; PORE-SIZE;
D O I
10.3389/fbioe.2023.1139649
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This work examined the physical and chemical properties and biocompatibility in vivo and in vitro of a unique triple composite scaffold incorporating silk fibroin, chitosan, and extracellular matrix. The materials were blended, cross-linked, and freeze-dried to create a composite scaffold of silk fibroin/chitosan/colon extracellular matrix (SF/CTS/CEM) with varying CEM contents. The SF/CTS/CEM (1:1:1) scaffold demonstrated the preferable shape, outstanding porosity, favorable connectivity, good moisture absorption, and acceptable and controlled swelling and degradation properties. Additionally, HCT-116 cells cultivated with SF/CTS/CEM (1:1:1) showed excellent proliferation capacity, cell malignancy, and delayed apoptosis, according to the in vitro cytocompatibility examination. We also examined the PI3K/PDK1/Akt/FoxO signaling pathway and discovered that cell culture using a SF/CTS/CEM (1:1:1) scaffold may prevent cell death by phosphorylating Akt and suppressing FoxO expression. Our findings demonstrate the potential of the SF/CTS/CEM (1:1:1) scaffold as an experimental model for colonic cancer cell culture and for replicating the three-dimensional in vivo cell growth environment.
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页数:13
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