Experimental study on co-culture of DiI labeled rat bone marrow mesenchymal stem cells and polycaprolactone film in vitro to make a cell patch.

IF 1 4区 医学 Q4 ENGINEERING, BIOMEDICAL
Zhang Zichang, Zhou Fan, Zheng Jianwei, Mu Junsheng, Bo Ping, You Bin
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引用次数: 1

Abstract

Background: In stem cell therapy, due to the lack of an effective carrier, a large number of transplanted stem cells are lost and die. Therefore, finding a suitable carrier has become a further direction of stem cell therapy.

Objective: In research on the co-culture of polycaprolactone (PCL) with 1,1'-Dioctadecyl-3,3,3',3'- tetramethylindocarbocyanine perchlorate (DiI) labeled bone marrow mesenchymal stem cells (BMSCs), we observe the effect of materials on the growth and proliferation of DiI labeled stem cells, and the effect of DiI labeling on patch preparation, so as to find a kind of biomaterial suitable for the growth and proliferation of BMSCs, and find a suitable cell carrier for stem cell therapy of myocardial infarction and in vivo tracing.

Methods: Clean grade Sprague Dawley rats were selected as experimental objects, BMSCs were isolated and cultured, and the surface markers were identified by flow cytometry. After the BMSCs were cultured for 3 passages, the BMSCs were stained with DiI dye, and the BMSCs DiI and PCL biomaterial film were co-cultured. After 24 hours, the cell growth was observed under fluorescence microscope, and fixed for scanning under electron microscope. The cell proliferation was detected by CCK-8 at 1, 4, 7, 10 days of culture. The measurement data conforming to normal distribution are expressed in the form of mean ± standard deviation (X¯± s). One way ANOVA was used for comparison among groups, LSD analysis was used for pairwise comparison. The difference was statistically significant (P < 0.05).

Results: BMSCs were strongly positive for CD90, CD44H, but negative for CD11b/c, CD45. Under fluorescence microscope, BMSCs DiI showed red light, fusiform or polygonal. Under the scanning electron microscope, the cell patch formed by co-culture of PCL film and DiI-BMSCs had a large number of cells on the surface and normal cell state. CCK-8 assay showed that the OD value on the first day was 0.330 ± 0.025; The OD value was 0.620 ± 0.012 on the 4th day, 1.033 ± 0.144 on the 7th day and 1.223 ± 0.133 on the 10th day. There was significant difference among the time points (P < 0.05).

Conclusions: The cell patch made of PCL film and DiI labeled BMSCs can survive and proliferate on the surface, so it can be used as a scaffold material for stem cell therapy in vivo.

DiI标记大鼠骨髓间充质干细胞与聚己内酯膜体外共培养制备细胞贴片的实验研究。
背景:在干细胞治疗中,由于缺乏有效的载体,大量移植的干细胞丢失和死亡。因此,寻找合适的载体成为干细胞治疗的进一步方向。摘要目的:在聚己内酯(PCL)与1,1′-二十八烷基-3,3,3′,3′-四甲基多碳青高氯酸盐(DiI)标记骨髓间充质干细胞(BMSCs)共培养的研究中,我们观察了材料对DiI标记干细胞生长和增殖的影响,以及DiI标记对贴片制备的影响,从而寻找一种适合BMSCs生长和增殖的生物材料。寻找适合心肌梗死干细胞治疗和体内追踪的细胞载体。方法:以洁净级大鼠为实验对象,分离培养骨髓间充质干细胞,采用流式细胞术对其表面标志物进行鉴定。培养3代后,对BMSCs进行DiI染色,将BMSCs DiI与PCL生物材料膜共培养。24h后在荧光显微镜下观察细胞生长情况,固定后在电镜下扫描。培养1、4、7、10 d时用CCK-8检测细胞增殖情况。符合正态分布的计量资料以均数±标准差(X¯±s)表示,组间比较采用单因素方差分析,两两比较采用LSD分析。结果:骨髓间充质干细胞CD90、CD44H呈强阳性,CD11b/c、CD45呈阴性。荧光显微镜下BMSCs DiI呈红光、梭形或多边形。扫描电镜下,PCL膜与DiI-BMSCs共培养形成的细胞斑块表面有大量细胞,细胞状态正常。CCK-8测定结果显示,第1天OD值为0.330±0.025;第4天OD值为0.620±0.012,第7天OD值为1.033±0.144,第10天OD值为1.223±0.133。结论:PCL膜与DiI标记的骨髓间充质干细胞制备的细胞贴片可在体外存活和增殖,可作为干细胞治疗的支架材料。
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来源期刊
Bio-medical materials and engineering
Bio-medical materials and engineering 工程技术-材料科学:生物材料
CiteScore
1.80
自引率
0.00%
发文量
73
审稿时长
6 months
期刊介绍: The aim of Bio-Medical Materials and Engineering is to promote the welfare of humans and to help them keep healthy. This international journal is an interdisciplinary journal that publishes original research papers, review articles and brief notes on materials and engineering for biological and medical systems. Articles in this peer-reviewed journal cover a wide range of topics, including, but not limited to: Engineering as applied to improving diagnosis, therapy, and prevention of disease and injury, and better substitutes for damaged or disabled human organs; Studies of biomaterial interactions with the human body, bio-compatibility, interfacial and interaction problems; Biomechanical behavior under biological and/or medical conditions; Mechanical and biological properties of membrane biomaterials; Cellular and tissue engineering, physiological, biophysical, biochemical bioengineering aspects; Implant failure fields and degradation of implants. Biomimetics engineering and materials including system analysis as supporter for aged people and as rehabilitation; Bioengineering and materials technology as applied to the decontamination against environmental problems; Biosensors, bioreactors, bioprocess instrumentation and control system; Application to food engineering; Standardization problems on biomaterials and related products; Assessment of reliability and safety of biomedical materials and man-machine systems; and Product liability of biomaterials and related products.
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