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不同蛋白酶水解乳清蛋白产物对3T3-E1成骨细胞增殖与分化的影响

Effects of the Whey Protein Hydrolysates of Various Protein Enzymes on the Proliferation and Differentiation of 3T3-E1 Osteoblasts.

作者信息

Jo Kyungae, Hong Ki-Bae, Suh Hyung Joo

机构信息

BK21Plus, College of Health Science, Korea University, Seoul 02841, Korea.

Department of Public Health Science, Korea University, Seoul 02841, Korea.

出版信息

Prev Nutr Food Sci. 2020 Mar 31;25(1):71-77. doi: 10.3746/pnf.2020.25.1.71.

Abstract

In this study, we used various proteinases to investigate the effect of whey protein hydrolysates on proliferation and differentiation of MC3T3-E1 osteoblasts. To confirm hydrolysis of the whey protein hydrolysates, the yield and α-amino acid content were determined. Since osteogenic cell activity is an important factor in osteogenesis, we evaluated the proliferation of osteogenic cells by measuring 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide and alkaline phosphatase (ALP) activity. To analyze bone matrix formation, we identified calcium deposition by staining with Alizaline red-S. The free amino acid content was significantly higher in the whey protein hydrolysates prepared using Protamex, Flavourzyme, and Alcalase than in the control. When cells were treated with 500 μg/mL of whey protein hydrolysates prepared using Protamex and Alcalase, cell proliferation increased by 120% and 130%, respectively, compared with the control group. In addition, ALP activity was significantly higher following treatment with 500 μg/mL of whey protein hydrolysates prepared using Protamex and Alcalase (142.61% and 135.06%, respectively; <0.05). Furthermore, when treated with 125 μg/mL of the same hydrolysates, the rate of calcium deposition increased significantly to 157.56% compared with the control group (<0.05). Therefore, our results suggest that whey protein hydrolysates prepared using Protamex and Alcalase may have more beneficial effects on osteoblast proliferation and bone health than those prepared using other proteolytic enzymes.

摘要

在本研究中,我们使用了多种蛋白酶来研究乳清蛋白水解物对MC3T3-E1成骨细胞增殖和分化的影响。为了确认乳清蛋白水解物的水解情况,测定了其产率和α-氨基酸含量。由于成骨细胞活性是骨生成的一个重要因素,我们通过测量3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑和碱性磷酸酶(ALP)活性来评估成骨细胞的增殖。为了分析骨基质形成,我们用茜素红-S染色鉴定钙沉积。使用Protamex、风味酶和碱性蛋白酶制备的乳清蛋白水解物中的游离氨基酸含量显著高于对照组。当用500μg/mL使用Protamex和碱性蛋白酶制备的乳清蛋白水解物处理细胞时,与对照组相比,细胞增殖分别增加了120%和130%。此外,用500μg/mL使用Protamex和碱性蛋白酶制备的乳清蛋白水解物处理后,ALP活性显著更高(分别为142.61%和135.06%;P<0.05)。此外,当用125μg/mL相同的水解物处理时,与对照组相比,钙沉积率显著增加至157.56%(P<0.05)。因此,我们的结果表明,使用Protamex和碱性蛋白酶制备的乳清蛋白水解物可能比使用其他蛋白水解酶制备的水解物对成骨细胞增殖和骨骼健康有更有益的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6762/7143006/7eed01d1dde5/PNFS-25-071-f1.jpg

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