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在炎症性肠病的临床前模型中对 tenascin C 的选择性拼接 D 结构域进行成像。

Imaging the Alternatively Spliced D Domain of Tenascin C in a Preclinical Model of Inflammatory Bowel Disease.

机构信息

AbbVie Bioresearch Center, 100 Research Dr, Worcester, MA, 01605, USA.

Bristol Myers Squibb, 100 Binney St, Cambridge, MA, 02142, USA.

出版信息

Mol Imaging Biol. 2023 Apr;25(2):314-323. doi: 10.1007/s11307-022-01758-6. Epub 2022 Jul 29.

Abstract

PURPOSE

To image colon-expressed alternatively spliced D domain of tenascin C in preclinical colitis models using near infrared (NIR)-labeled targeted molecular imaging agents.

PROCEDURES

A human IgG1 with nanomolar binding affinity specific to the alternatively spliced D domain of tenascin C was generated. Immunohistochemistry identified disease-specific expression of this extracellular matrix protein in the colon of mice given dextran sulfate sodium in the drinking water. The antibody reagent was labeled with the NIR fluorophore IRDye 800CW via amine chemistry and intravenously dosed to evaluate in vivo targeting specificity. Increasing doses of imaging agent were given to estimate the saturating dose.

RESULTS

The NIR-labeled proteins successfully targeted colonic lesions in a murine model of colitis. Co-administration of a molar excess competing unlabeled dose reduced normalized uptake in diseased colon by > 70%. Near infrared ex vivo images of colon resected from diseased animals showed saturation at doses exceeding 1 nmol and was confirmed with additional quantitative ex vivo biodistribution. Cellular-level specificity and protein stability were assessed via microscopy.

CONCLUSIONS

Our imaging data suggest the alternatively spliced D domain of tenascin C is a promising target for delivery-based applications in inflammatory bowel diseases.

摘要

目的

使用近红外(NIR)标记的靶向分子成像剂在临床前结肠炎模型中对结肠表达的 tenascin C 选择性剪接 D 结构域进行成像。

方法

生成了与人 tenascin C 选择性剪接 D 结构域具有纳摩尔结合亲和力的人 IgG1。免疫组织化学鉴定出在给予饮用水中硫酸葡聚糖钠的小鼠的结肠中,这种细胞外基质蛋白具有疾病特异性表达。通过胺化学将抗体试剂用近红外荧光染料 IRDye 800CW 标记,并静脉内给药以评估体内靶向特异性。给予递增剂量的成像剂以估计饱和剂量。

结果

NIR 标记的蛋白质成功地靶向了结肠炎小鼠模型中的结肠病变。共给予摩尔过量的竞争未标记剂量可使患病结肠的归一化摄取减少>70%。来自患病动物的切除结肠的近红外离体图像显示在超过 1nmol 的剂量下达到饱和,并通过额外的定量离体生物分布得到证实。通过显微镜评估了细胞水平的特异性和蛋白质稳定性。

结论

我们的成像数据表明,tenascin C 的选择性剪接 D 结构域是炎症性肠病中基于递药应用的有前途的靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5c2/10006278/84fb0d4edb29/11307_2022_1758_Fig1_HTML.jpg

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