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利用荧光标记的八聚精氨酸与糖胺聚糖的结合特性对小鼠关节软骨进行光学成像。

Optical imaging of mouse articular cartilage using the glycosaminoglycans binding property of fluorescent-labeled octaarginine.

机构信息

Department of Molecular Biology and Biochemistry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

出版信息

Osteoarthritis Cartilage. 2009 Sep;17(9):1209-18. doi: 10.1016/j.joca.2009.03.010. Epub 2009 Mar 24.

Abstract

OBJECTIVE

The aim of the current study was to examine the cartilage-specific binding property of polyarginine peptides (R4, 8, 12, and 16) and specifically to test octaarginine peptides for the optical imaging of articular cartilage in experimentally induced arthritis in mice.

METHODS

Four rhodamine-labeled polyarginine peptides each with a different-length arginine chain (R4, 8, 12, or 16) were injected into the knee joints of C57BL/6J mice (n=20). The joints were excised 1h later and the fluorescent signal intensity in cartilage cryosections was compared for the four peptides. To examine the substrate of R8 in cartilage, femoral condyles obtained from another set of mice were treated with chondroitinase ABC (Ch'ase ABC), keratanase or heparitinase then immersed in R8-rhodamine. Fluorescent signals were examined by fluorescent microscopy. Next, R8-rhodamine was injected into the right knee joints of three control and three collagen antibody-induced arthritis (CAIA) mice, and fluorescent intensity in normal and degenerative cartilage was semi-quantitatively analysed on the histological sections using image software. Finally, femoral condyles from normal mice (n=2) and CAIA mice (n=2) were immersed in R8-rhodamine and calcein, then imaged using optical projection tomography (OPT).

RESULTS

Fluorescent signals were specifically detected in the cartilage pericellular matrix from the surface to the tide mark but were completely absent in the calcified layer or bone marrow. The number of arginine residues significantly influenced peptide accumulation in articular cartilage, with R8 accumulating the most. The fluorescent signal in the femoral condylar cartilage diminished when it was treated with Ch'ase ABC. R8 accumulation was significantly decreased in the degenerative cartilage of CAIA mice, and this was demonstrated both histologically and in three-dimensional (3D)-reconstruction image by OPT.

CONCLUSION

R8 may be a useful new experimental probe for optical imaging of normal and arthritic articular cartilage.

摘要

目的

本研究旨在探讨聚精氨酸肽(R4、8、12 和 16)的软骨特异性结合特性,并特别测试八精氨酸肽在实验性关节炎小鼠关节软骨的光学成像中的应用。

方法

将四种不同长度精氨酸链的罗丹明标记聚精氨酸肽(R4、8、12 或 16)分别注入 C57BL/6J 小鼠膝关节(n=20)。1 小时后取出关节,比较四种肽在软骨冷冻切片中的荧光信号强度。为了研究 R8 在软骨中的结合底物,将另一组小鼠的股骨髁用软骨素酶 ABC(Ch'ase ABC)、角蛋白酶或肝素酶处理,然后浸入 R8-罗丹明中。通过荧光显微镜检查荧光信号。接下来,将 R8-罗丹明注入三组对照和三组胶原抗体诱导关节炎(CAIA)小鼠的右膝关节,并用图像软件对半定量分析正常和退行性软骨的组织切片中的荧光强度。最后,将正常小鼠(n=2)和 CAIA 小鼠(n=2)的股骨髁浸入 R8-罗丹明和钙黄绿素中,然后使用光学投影断层扫描(OPT)成像。

结果

荧光信号特异性地在软骨细胞外基质中从表面到潮标线检测到,但在钙化层或骨髓中完全不存在。精氨酸残基的数量显著影响关节软骨中肽的积累,其中 R8 积累最多。用 Ch'ase ABC 处理后,股骨髁软骨中的荧光信号减弱。CAIA 小鼠退行性软骨中 R8 的积累明显减少,这在组织学和 OPT 三维(3D)重建图像中都得到了证明。

结论

R8 可能是一种用于正常和关节炎关节软骨光学成像的有用的新实验探针。

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