Chitin powder enhances growth factor production and therapeutic effects of mesenchymal stem cells in a chronic kidney disease rat model

被引:2
作者
Hori, Hideo [1 ]
Sakai, Kazuyoshi [2 ]
Ohashi, Atsushi [2 ]
Nakai, Shigeru [2 ]
机构
[1] Fujita Hlth Univ, Fac Med Technol, Sch Med Sci, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Aichi 4701192, Japan
[2] Fujita Hlth Univ, Fac Clin Engn, Sch Med Sci, 1-98 Dengakugakubo,Kutsukake Cho, Toyoake, Aichi 4701192, Japan
关键词
Mesenchymal stem cell; Chitin powder; Hepatocyte growth factor; Vascular endothelial growth factor; PERIPHERAL-BLOOD CELLS; OXIDATIVE STRESS; NONWOVEN FILTERS; INJURY; SCAFFOLDS; PODOCYTE; SURVIVAL; TNF;
D O I
10.1007/s10047-022-01346-z
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Previously, we fabricated a device with polylactic acid nonwoven filters and mesenchymal stem cells (MSCs), which effectively reduced urinary protein levels in a rat model of chronic kidney disease (CKD) but could not suppress CKD progression. Therefore, to improve the therapeutic effects of MSCs, in this study, we analyzed the ability of rat adipose tissue-derived MSCs (ADSCs) in contact with chitin nonwoven filters or chitin powder to produce growth factors and examined their therapeutic effect in an adriamycin (ADR)-induced CKD rat model. Hepatocyte growth factor (HGF) and vascular endothelial growth factor (VEGF) production was significantly enhanced by ADSCs cultured in a medium containing chitin powder (C-ADSCs) compared with that by ADSCs cultured in a standard medium without chitin (N-ADSCs). However, the production of HGF and VEGF by ADSCs on chitin nonwoven filters was not significantly enhanced compared with that by the control. Intravenous C-ADSC injection significantly increased podocin expression and improved proteinuria compared with those in saline-treated CKD rats; however, no such improvements were observed in the N-ADSC-treated group. These results showed that ADSCs cultured in a medium supplemented with chitin powder suppressed proteinuria via enhanced HGF and VEGF production in ADR-induced CKD rats to mitigate podocyte damage, offering a new strategy to reduce the dose of MSC therapy for safe and effective treatment of kidney disease.
引用
收藏
页码:203 / 211
页数:9
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