Supplementary MaterialsSupplementary material mmc1. their tissues were observed; Roscovitine supplier rLj-RGD3 was labeled with FITC and then added into the HeyA8 cells. The location of rLj-RGD3 was observed by a confocal laser scanning microscope. /em Data source location em Dalian, China /em Data accessibility em Data are available with this article. /em Open in a separate window Value of the data ? The data are valuable for the safety of rLj-RGD3 treatment in rats which were bearing tumors.? The data are valuable for the acute toxicity of rLj-RGD3 Roscovitine supplier in rats.? The data are beneficial for the positioning of rLj-RGD3 in the HeyA8 cells. 1.?Data The info of this content provide the cells observation of Sprague Dawley (SD) rats which were treated with regular saline (NS) or rLj-RGD3. Fig. 1 demonstrated the lungs, hearts, livers, kidneys and spleens that have been isolated from NS or rLj-RGD3 treated SD rats. Furthermore, confocal microscope data had been shown to take notice of the area of FITC-labeled rLj-RGD3 in the HeyA8 cells (Fig. 2). Open up in another home window Fig. 1 Cells including lungs, hearts, livers, spleens and kidneys had been shown following the SD rats had been injected with NS and 20 intravenously?mg/kg rLj-RGD3, respectively. Open up in another home window Fig. 2 The positioning of FITC-labeled rLj-RGD3 in the HeyA8 cells. 2.?Experimental design, methods and materials 2.1. Protection evaluation of rLj-RGD3 treatment in SD rats Acute toxicity of rLj-RGD3 was performed in Center for Protection Evaluation and Study of Medicines, Institute of Roscovitine supplier Lab Animal Technology (ILAS), Chinese language Academy of Medical Sciences (GLP11001029). 40?SD rats (20 men and 20 females) with age 6 weeks were random split into two organizations. Subsequently, these rats had been intravenously injected with NS (adverse control, 10 men and 10 females) and 20?mg/kg rLj-RGD3 (1000 moments of clinical dose of Roscovitine supplier rLj-RGD3, 20?g/kg, 10 men and 10 females), respectively. After 15 times, these mice had been sacrificed as well as the cells had been noticed. 2.2. Cell tradition DMEM (GIBCO, USA) including 10% (vol/vol) fetal bovine serum (FBS, GIBCO) was utilized to tradition HeyA8 cells inside a humidified incubator with 5% CO2 at 37?C [1]. 2.3. Fluorescent labeling and staining Based on the producer?s guidelines, the purified rLj-RGD3 was blended with FITC (HOOK? FITC Labeling Package, G Biosciences) which really is a popular reagent for labeling proteins. After eliminating the unconjugated dye, the tagged rLj-RGD3 (6?M, last concentration) was added into the HeyA8 cells for 1?h. Subsequently, these HeyA8 cells were fixed with 4% paraformaldehyde for 10?min. Next, the HeyA8 cells were washed with PBS twice and observed by a laser scanning confocal microscope (Carl Zeiss, Germany) at 400 magnification. Acknowledgments This work was supported by grants from The National High Technology Research and Development Program (863 Program, No. SS2014AA091602), National Natural Science Foundation of China (No. 31301880), China Postdoctoral Science Foundation (No. 2013M541246), Program for Liaoning Excellent Talents in University (LJQ2015057), and Dalian High Level Talent Innovation Support Plan (No. 2015R067). Footnotes Transparency documentTransparency data associated with this article can be found in the online version at doi:10.1016/j.dib.2017.03.033. Transparency document.?Supplementary material Supplementary material Click here to view.(13K, docx) . Reference 1. Jiang Q., Li Q., Han J., Gou M., Zheng Y., Li B., Xiao R., Wang J. rLj-RGD3 induces apoptosis via the mitochondrial-dependent pathway and inhibits adhesion, migration and invasion of human HeyA8 cells Rabbit polyclonal to ACVR2B via FAK pathway. Int. J. Biol. Macromol. 2017;96:652C668. [PubMed] [Google Scholar].
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