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封装的基质衍生因子1α的控释改善骨髓间充质基质细胞迁移。

Controlled Release of Encapsuled Stromal-Derived Factor 1α Improves Bone Marrow Mesenchymal Stromal Cells Migration.

作者信息

Bajdak-Rusinek Karolina, Fus-Kujawa Agnieszka, Jelonek Katarzyna, Musiał-Kulik Monika, Buszman Piotr Paweł, Żyła-Uklejewicz Dorota, Sekowska Adrianna Walentyna, Kasperczyk Janusz, Buszman Paweł Eugeniusz

机构信息

Department of Medical Genetics, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Medykow 18 Street, 40-752 Katowice, Poland.

Center of Polymer and Carbon Materials, Polish Academy of Sciences, M. Curie-Sklodowskiej 34, 41-819 Zabrze, Poland.

出版信息

Bioengineering (Basel). 2022 Dec 2;9(12):754. doi: 10.3390/bioengineering9120754.

DOI:10.3390/bioengineering9120754
PMID:36550960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9774977/
Abstract

Stem cell treatment is a promising method of therapy for the group of patients whose conventional options for treatment have been limited or rejected. Stem cells have the potential to repair, replace, restore and regenerate cells. Moreover, their proliferation level is high. Owing to these features, they can be used in the treatment of numerous diseases, such as cancer, lung diseases or ischemic heart diseases. In recent years, stem cell therapy has greatly developed, shedding light on stromal-derived factor 1α (SDF-1α). SDF-1α is a mobilizing chemokine for application of endogenous stem cells to injury sites. Unfortunately, SDF-1α presented short-term results in stem cell treatment trials. Considering the tremendous benefits of this therapy, we developed biodegradable polymeric microspheres for the release of SDF-1α in a controlled and long-lasting manner. The microspheres were designed from poly(L-lactide/glycolide/trimethylene carbonate) (PLA/GA/TMC). The effect of controlled release of SDF-1α from microspheres was investigated on the migration level of bone marrow Mesenchymal Stromal Cells (bmMSCs) derived from a pig. The study showed that SDF-1α, released from the microspheres, is more efficient at attracting bmMSCs than SDF-1α alone. This may enable the controlled delivery of selected and labeled MSCs to the destination in the future.

摘要

对于那些传统治疗选择有限或已被拒绝的患者群体而言,干细胞治疗是一种很有前景的治疗方法。干细胞具有修复、替代、恢复和再生细胞的潜力。此外,它们的增殖水平很高。由于这些特性,它们可用于治疗多种疾病,如癌症、肺部疾病或缺血性心脏病。近年来,干细胞治疗有了很大发展,对基质衍生因子1α(SDF-1α)有了新的认识。SDF-1α是一种趋化因子,可将内源性干细胞募集到损伤部位。遗憾的是,SDF-1α在干细胞治疗试验中呈现出短期效果。鉴于这种治疗方法的巨大益处,我们开发了可生物降解的聚合物微球,用于以可控且持久的方式释放SDF-1α。这些微球由聚(L-丙交酯/乙交酯/三亚甲基碳酸酯)(PLA/GA/TMC)制成。研究了从微球中可控释放SDF-1α对猪源骨髓间充质基质细胞(bmMSCs)迁移水平的影响。研究表明,从微球中释放的SDF-1α在吸引bmMSCs方面比单独的SDF-1α更有效。这可能使未来能够将经过选择和标记的间充质干细胞可控地输送到目标部位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/03ddff21affe/bioengineering-09-00754-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/217a057af015/bioengineering-09-00754-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/7e7bec61ea47/bioengineering-09-00754-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/5b545f4ad679/bioengineering-09-00754-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/2074e111bebe/bioengineering-09-00754-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/739763833607/bioengineering-09-00754-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/012bc85131d3/bioengineering-09-00754-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/a253aa11baf2/bioengineering-09-00754-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/03ddff21affe/bioengineering-09-00754-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/217a057af015/bioengineering-09-00754-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/7e7bec61ea47/bioengineering-09-00754-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/5b545f4ad679/bioengineering-09-00754-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/2074e111bebe/bioengineering-09-00754-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/739763833607/bioengineering-09-00754-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/012bc85131d3/bioengineering-09-00754-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/a253aa11baf2/bioengineering-09-00754-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f98/9774977/03ddff21affe/bioengineering-09-00754-g008.jpg

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