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Recognition of dextran-superparamagnetic iron oxide nanoparticle conjugates (Feridex) via macrophage scavenger receptor charged domains

机译:葡聚糖 - 超顺磁氧化物纳米颗粒缀合物的识别(菲立磁)通过巨噬细胞清除受体带电域

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摘要

Dextran-coated superparamagnetic iron oxide nanoparticles (dextran-SPIO conjugates) offer the attractive possibility of enhancing MRI imaging sensitivity so that small or diffuse lesions can be detected. However, systemically injected SPIO are rapidly removed by macrophages. We engineered embryonic cells (HEK293T) to express major macrophage scavenger receptor (SR) subtypes including SR-AI, MARCO, and endothelial receptor collectin-12. These SRs possess a positively charged collagen-like (CL) domain and they promoted SPIO uptake, while the charge neutral lipoprotein receptor SR-BI did not. In silico modeling indicated a positive net charge on the CL domain, and a net negative charge on the cysteine-rich (CR) domain of MARCO and SR-AI. In vitro experiments revealed that CR domain deletion in SR-AI boosted uptake of SPIO 3-fold, while deletion of MARCO's CR domain abolished this uptake. These data suggest that future studies might productively focus on the validation and further exploration of SR charge fields in SPIO recognition.
机译:涂葡聚糖的超顺磁性氧化铁纳米颗粒(葡聚糖-Spio缀合物)提供了提高MRI成像敏感性的有吸引力的可能性,以便可以检测到小或漫射病变。然而,通过巨噬细胞迅速除去系统性注射的硅藻。我们设计胚胎细胞(HEK293T)以表达主要的巨噬细胞清除剂受体(SR)亚型,包括SR-AI,MARCO和内皮受体收集蛋白-12。这些SRS具有带正电荷的胶原蛋白(CL)域,它们促进了斯凯术,而电荷中性脂蛋白受体SR-BI没有。在硅建模中,表明CL结构域的正净电荷,以及MARCO和SR-AI的半胱氨酸 - 富含半胱氨酸(CR)结构域的净负电荷。体外实验表明,SR-AI中的Cr结构域缺失增强了Spio 3折的摄取,而Marco的CR域取消了这种摄取。这些数据表明,未来的研究可能会富有力地关注SPIO识别中SR电荷领域的验证和进一步探索。

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