Cholesterol-linoleic acid liposomes induced extracellular vesicles secretion from immortalized adipose-derived mesenchymal stem cells for in vitro cell migration

被引:1
|
作者
Chen, Jzit Weii [1 ]
Liew, Fong Fong [2 ]
Tan, Hsiao Wei [3 ]
Misran, Misni [4 ]
Chung, Ivy [1 ]
机构
[1] Univ Malaya, Fac Med, Dept Pharmacol, Kuala Lumpur, Malaysia
[2] MAHSA Univ, Fac Dent, Dept Oral Biol & Biomed Sci, Jenjarom, Selangor, Malaysia
[3] Univ Malaya, Inst Res Management & Serv, Res & Innovat Management Complex, Kuala Lumpur, Malaysia
[4] Univ Malaya, Fac Sci, Dept Chem, Kuala Lumpur, Malaysia
关键词
Cholesterol; extracellular vesicles; immortalized AD-MSCs; liposomes; regenerative medicine; DRUG-DELIVERY; CATIONIC LIPOSOMES; EXOSOMES; MEMBRANE; CHARGE; COMMUNICATION; GENERATION; MEDICINE; SYSTEM;
D O I
10.1080/21691401.2023.2237534
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
Extracellular vesicles (EVs) are small vesicles that are naturally released by cells and play a crucial role in cell-to-cell communication, tissue repair and regeneration. As naturally secreted EVs are limited, liposomes with different physicochemical properties, such as 1,2-dioleoyl-3-trimethylammonium propane (DOTAP) and linoleic acid (LA) with modifications have been formulated to improve EVs secretion for in vitro wound healing. Various analyses, including dynamic light scattering (DLS) and transmission electron microscopy (TEM) were performed to monitor the successful preparation of different types of liposomes. The results showed that cholesterol-LA liposomes significantly improved the secretion of EVs from immortalized adipose-derived mesenchymal stem cells (AD-MSCs) by 1.5-fold. Based on the cell migration effects obtained from scratch assay, both LA liposomal-induced EVs and cholesterol-LA liposomal-induced EVs significantly enhanced the migration of human keratinocytes (HaCaT) cell line. These findings suggested that LA and cholesterol-LA liposomes that enhance EVs secretion are potentially useful and can be extended for various tissue regeneration applications.
引用
收藏
页码:346 / 360
页数:15
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