| Literature DB >> 35484464 |
Yu Zhang1, Lijuan Jiao1, Lin Lu1, Chengjie Wu1, Junchu Tu1, Yujie Li1, Yanli Wang1, Fengzhi Ding1, Wei Luo1, Wenjie Chen1, Zhenya Shen1, Yao-Hua Song2,3, Yangxin Li4.
Abstract
Ischemic diseases are life-threatening, and the incidence increases as people's lifestyles change. Medications and surgical intervention offer limited benefit, and stem cell therapy has emerged as a potential approach for treating ischemic diseases. The exosomes secreted by stem cells have attracted more attention because they do not trigger the immune response and can be used as drug carriers. The non-coding RNA (ncRNA) carried by exosomes plays a key role in mediating exosome's beneficial effect, which can be further enhanced when combined with nanomaterials to improve its retention time. Here, we review the downstream target molecules and signal pathways of ncRNA and summarize recent advances of some nanomaterials used to encapsulate exosomes and promote ischemic tissue repair. We highlight the imprinting of exosomes from parent cells and discuss how the inflammasome pathway may be targeted for the development of novel therapy for ischemic diseases.Entities:
Keywords: Exosome; Inflammasome; Ischemic diseases; Nanomaterial; ncRNA
Mesh:
Year: 2022 PMID: 35484464 DOI: 10.1007/s12265-022-10263-8
Source DB: PubMed Journal: J Cardiovasc Transl Res ISSN: 1937-5387 Impact factor: 3.216