Evaluating the pro-survival potential of apoptotic bodies derived from 2D- and 3D- cultured adipose stem cells in ischaemic flaps

脂肪组织 细胞凋亡 氧化应激 干细胞 血管生成 小RNA 细胞生物学 移植 程序性细胞死亡 炎症 坏死 生物 癌症研究 医学 免疫学 病理 外科 内分泌学 生物化学 基因
作者
Gaoxiang Yu,Jian Ding,Ningning Yang,Lu Ge,Nuo Chen,Xuzi Zhang,Qiuchen Wang,Xian Liu,Xuanlong Zhang,Xiaoqiong Jiang,Yibo Geng,Chenxi Zhang,Jiadong Pan,Xiangyang Wang,Weiyang Gao,Zhijie Li,Hongyu Zhang,Wenfei Ni,Jian Xiao,Kailiang Zhou
出处
期刊:Journal of Nanobiotechnology [BioMed Central]
卷期号:22 (1): 333-333 被引量:39
标识
DOI:10.1186/s12951-024-02533-1
摘要

In the realm of large-area trauma flap transplantation, averting ischaemic necrosis emerges as a pivotal concern. Several key mechanisms, including the promotion of angiogenesis, the inhibition of oxidative stress, the suppression of cell death, and the mitigation of inflammation, are crucial for enhancing skin flap survival. Apoptotic bodies (ABs), arising from cell apoptosis, have recently emerged as significant contributors to these functions. This study engineered three-dimensional (3D)-ABs using tissue-like mouse adipose-derived stem cells (mADSCs) cultured in a 3D environment to compare their superior biological effects against 2D-ABs in bolstering skin flap survival. The findings reveal that 3D-ABs (85.74 ± 4.51) % outperform 2D-ABs (76.48 ± 5.04) % in enhancing the survival rate of ischaemic skin flaps (60.45 ± 8.95) % (all p < 0.05). Mechanistically, they stimulated angiogenesis, mitigated oxidative stress, suppressed apoptosis, and facilitated the transition of macrophages from M1 to M2 polarization (all p < 0.05). A comparative analysis of microRNA (miRNA) profiles in 3D- and 2D-ABs identified several specific miRNAs (miR-423-5p-up, miR30b-5p-down, etc.) with pertinent roles. In summary, ABs derived from mADSCs cultured in a 3D spheroid-like arrangement exhibit heightened biological activity compared to those from 2D-cultured mADSCs and are more effective in promoting ischaemic skin flap survival. These effects are attributed to their influence on specific miRNAs.
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