天花板培养衍生的增生性脂肪细胞是卵磷脂:胆固醇酰基转移酶缺乏症的酶替代治疗的可能递送载体

Masayuki Kuroda, Y. Aoyagi, Sakiyo Asada, H. Bujo, Shigeaki Tanaka, T. Konno, M. Tanio, I. Ishii, K. Machida, F. Matsumoto, K. Satoh, Masayuki Aso, Y. Saito
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引用次数: 22

摘要

通过天花板培养技术从皮下脂肪组织(被称为ccdPA)中增殖的人类增生性脂肪细胞在此被评估其作为逆转录病毒载体介导的治疗性蛋白质传递的基因转导受体的潜力。使用由7天天花板培养产生的细胞制剂暴露于表达zsgreen的载体上清可诱导40-50%的转导效率,平均每个细胞少于两个完整的病毒基因组拷贝。lcat基因转导的人ccdPA分泌功能的lcat蛋白,与载体基因组的整合拷贝数相关。在脂肪组织制备后的一个月内,基因转导的细胞可以从1克脂肪组织扩增到近10 12个细胞。这些细胞在体外也保持了向脂肪细胞分化的潜力。将表达LCAT的ccdPA移植到免疫缺陷小鼠的脂肪组织中,免疫鉴定血清中存在人LCAT蛋白。这些结果表明,人ccdPA对lcat缺陷患者具有新的治疗潜力。结合细胞移植的临床应用为lcat缺陷患者的终身蛋白替代疗法的发展提供了线索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ceiling Culture-Derived Proliferative Adipocytes are A Possible Delivery Vehicle for Enzyme Replacement Therapy in Lecithin: Cholesterol Acyltransferase Deficiency
Human proliferative adipocytes propagated via ceiling culture technique from subcutaneous fat tissue (desig- nated as ccdPA) were herein evaluated for their potential as a recipient for retroviral vector-mediated gene transduction of a therapeutic protein delivery. Exposure to the ZsGreen-expressing vector supernatant using a cell preparation generated by a 7-day ceiling culture induced a 40-50% transduction efficiency, with less than two integrated copies of viral genome per cell on average. The lcat gene-transduced human ccdPA secreted functional LCAT protein, correlating with the inte- grated copy number of vector genome. The gene-transduced cells could be expanded up to nearly 10 12 cells from 1 g of fat tissue within one month after fat tissue preparation. The cells also maintained the potential to differentiate into adipocytes in vitro. The presence of human LCAT protein in serum was immunologically identified upon transplantation of lcat- expressing ccdPA into the adipose tissue of immune-deficient mice. These results indicated that human ccdPA has a novel therapeutic potential for LCAT-deficient patients. The clinical application in combination with cell transplantation shed a light on a development of a life-long protein replacement therapy for LCAT-deficient patients.
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