Biophysics, School of Physics, University of Exeter, Exeter EX4 4QL, UK.
J Anat. 2009 Dec;215(6):682-91. doi: 10.1111/j.1469-7580.2009.01149.x. Epub 2009 Oct 1.
A combination of two-photon fluorescence (TPF), second harmonic generation (SHG) and coherent anti-Stokes Raman scattering (CARS) imaging has been used to investigate the elastin fibre network in healthy equine articular cartilage from the metacarpophalangeal joint. The elastin fibres were identified using their intrinsic two-photon fluorescence and immuno-staining was used to confirm the identity of these fibres. SHG was used to reveal the collagen matrix and the collagen fibre orientations were determined from their SHG polarization sensitivity, while CARS was used to clearly delineate the cell boundaries. Extensive elastin fibre networks were found in all the joint regions investigated. The elastin was found predominantly in the superficial zone (upper 50 microm) and was aligned parallel to the articular surface. Elastin was also detected in the pericellular matrix surrounding the superficial chondrocytes; however, individual fibres could not be resolved in this region. Variations in the density and organization of the fibres were observed in different regions on the joint surface.
双光子荧光(TPF)、二次谐波产生(SHG)和相干反斯托克斯拉曼散射(CARS)成像的组合已被用于研究来自掌指关节的健康马关节软骨中的弹性纤维网络。使用其固有双光子荧光来鉴定弹性纤维,并使用免疫染色来确认这些纤维的身份。SHG 用于揭示胶原基质,并且从其 SHG 偏振灵敏度确定胶原纤维取向,而 CARS 用于清晰描绘细胞边界。在研究的所有关节区域都发现了广泛的弹性纤维网络。弹性蛋白主要存在于浅层(上层 50 微米),并与关节表面平行排列。弹性蛋白也在围绕浅层软骨细胞的细胞外基质中检测到;然而,在该区域无法分辨单个纤维。在关节表面的不同区域观察到纤维的密度和组织的变化。