Liraglutide modulates adhesion molecules and enhances cell properties in three-dimensional cultures of olfactory ensheathing cells

被引:1
|
作者
Tseng, Yu-Ting [1 ,2 ,3 ]
Lai, Richard [2 ]
Oieni, Francesca [1 ,2 ]
Standke, Andrea [1 ,2 ]
Smyth, Graham [1 ,2 ]
Yang, Chenying [1 ,2 ]
Chen, Mo [1 ,2 ,3 ,4 ]
St John, James [1 ,2 ,3 ,4 ]
Ekberg, Jenny [1 ,2 ,3 ,4 ]
机构
[1] Griffith Univ, Clem Jones Ctr Neurobiol & Stem Cell Res, Brisbane, Qld 4111, Australia
[2] Griffith Univ, Menzies Hlth Inst Queensland, Southport, Qld 4222, Australia
[3] Griffith Univ, Griffith Inst Drug Discovery, Brisbane, Qld 4111, Australia
[4] Griffith Univ, Gold Coast Campus,Parklands Dr, Southport, Qld 4222, Australia
基金
英国医学研究理事会;
关键词
Glia; Cell transplantation; GLP-1R; 3D spheroids; N-cadherin; 131-integrin; SPINAL-CORD-INJURY; SPHEROID FORMATION; MIGRATION; CADHERIN; GLIA; TRANSPLANTATION; PROLIFERATION; DEGENERATION; RAT;
D O I
10.1016/j.biopha.2023.115084
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cell transplantation using olfactory ensheathing cells (OECs) is a promising approach for nerve repair but there are numerous limitations with their delivery method. Three-dimensional (3D) cell culture systems potentially offer a powerful approach for cell production and delivery options. To further optimise the use of OECs, strategies to promote cell viability and maintain cell behaviours in 3D cultures become important. We previously demonstrated an anti-diabetic drug, liraglutide, could modulate OEC migration and re-model extracellular matrix in two-dimensional (2D) cultures. In the present study, we further investigated its beneficial effects in our 3D culture system using primary OECs. OECs treated with liraglutide at 100 nM showed improved cell viability and had modulated expression of N-cadherin and 131-integrin (two important cell adhesion molecules). When formed into 3D spheroids, the pre-treated OECs generated spheroids with an increased volume and a decreased cell density compared to control spheroids. OECs that subsequently migrated out of the liraglutide pre-treated spheroids had higher capacity for migration with increased duration and length, which was attributed to a reduction in the pauses during the migration. Moreover, OECs that migrated out from liraglutide spheroids had a more bipolar morphology consistent with higher migratory capacity. In summary, liraglutide improved the viability of OECs, modulated cell adhesion molecules, and resulted in stable 3D cell constructs which conferred enhanced migratory capacity on the OECs. Overall, liraglutide may potentially improve the therapeutic use of OECs for neural repair by enhancing the generation of stable 3D constructs and increasing the migratory behaviour of OECs.
引用
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页数:13
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