Stem Cell Membrane-Camouflaged Biomimetic Nanoparticles Inhibiting Leptin Pathway for Intervertebral Disc Degeneration Therapy

被引:0
作者
Wang, Zhe [1 ,2 ]
Qi, Lin [1 ,2 ]
Huang, Yong [1 ,2 ]
Liu, Zheng [1 ,2 ]
Wu, Ruibang [1 ,2 ]
Zhao, Yize [1 ,2 ]
Li, Hao [1 ,2 ]
Wang, Siyi [1 ,2 ]
Liu, Limin [1 ,2 ]
Zhang, Li [1 ,2 ]
Feng, Ganjun [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Analyt & Testing Ctr, Dept Orthoped Surg, Chengdu 610065, Peoples R China
[2] Sichuan Univ, West China Hosp, Orthoped Res Inst, Analyt & Testing Ctr, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
Intervertebral disc degeneration (IDD); Stem cell membrane; ZIF-8; Plasmid; Leptin; EXPRESSION; CHONDROCYTES; DELIVERY;
D O I
10.1021/acsami.4c15099
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Leptin, a kind of adipokine, with its receptor in which the long isoform plays a crucial role in signal transduction, has been identified in intervertebral disc (IVD) tissues, especially showing an increased expression in degenerated discs. Initially identified as a metabolic sensor, leptin has recently been found able to regulate inflammation into imbalance, which favors catabolic degradative processes, thus contributing to progressive intervertebral disc degeneration (IDD). Therefore, efficiently inhibiting the leptin pathway may provide a new strategy to treat IDD. In this study, we introduced an innovative drug delivery system (DDS) that employs stem cell membranes (SCM) to encapsulate (Zeolitic imidazolate frameworks-8) ZIF-8 nanoparticles. These nanoparticles are used to transport a plasmid containing shRNA targeting the leptin receptor (LEPR), with the aim of facilitating repair in IDD. The regenerative performances of this DDS in IDD were verified through a combination of the in vitro western blot and immunofluorescence with the in vivo radiologic examination and histological staining. The DDS demonstrated excellent cell adhesion properties and gene transfection efficiency in vitro, along with impressive treatment outcomes in vivo. Both in vitro and in vivo studies revealed that the DDS effectively reduced leptin receptor expression and alleviated the inflammatory environment, thereby promoting regeneration in degenerated IVDs. We propose that the DDS represents a promising novel approach for treating IDD and may also be beneficial for other degenerative diseases linked to leptin pathway dysfunction.
引用
收藏
页码:63333 / 63344
页数:12
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