冠状面
组织病理学
医学
H&E染色
增生
病理
骨关节炎
纤维化
分级(工程)
滑膜
矢状面
病态的
染色
解剖
关节炎
生物
内科学
生态学
替代医学
作者
Alia M. Obeidat,Sung Yeon Kim,Kevin G. Burt,Baofeng Hu,Jun Li,Shingo Ishihara,Rui Xiao,Rachel E. Miller,Christopher B. Little,Anne‐Marie Malfait,Carla R. Scanzello
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2023-10-18
被引量:1
标识
DOI:10.1101/2023.10.14.562259
摘要
ABSTRACT Background Synovial pathology has been linked to osteoarthritis (OA) pain in patients. Microscopic grading systems for synovial changes in human OA have been described, but a standardized approach for murine models of OA is needed. We sought to develop a reproducible approach and set of minimum recommendations for synovial histopathology in mouse models of OA. Methods Coronal and sagittal sections from male mouse knee joints subjected to destabilization of medial meniscus (DMM) or partial meniscectomy (PMX) were collected as part of other studies. Stains included Hematoxylin and Eosin (H&E), Toluidine Blue (T- Blue) and Safranin O/Fast Green (Saf-O). Four blinded readers graded pathological features (hyperplasia, cellularity, and fibrosis) at specific anatomic locations in the medial and lateral compartments. Inter-reader reliability of each feature was determined. Results There was acceptable to very good agreement between raters. After DMM, increased hyperplasia and cellularity and a trend towards increased fibrosis were observed 6 weeks after DMM in the medial locations, and persisted up to 16 weeks. In the PMX model, cellularity and hyperplasia were evident in both medial and lateral compartments while fibrotic changes were largely seen on the medial side. Synovial changes were consistent from section to section in the mid-joint area mice. H&E, T-blue, and Saf-O stains resulted in comparable reliability. Conclusions To allow for a standard evaluation that can be implemented and compared across labs and studies, we recommend using 3 readers to evaluate a minimum set of 3 pathological features at standardized anatomic areas. Pre-defining areas to be scored, and reliability for each pathologic feature should be considered.
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