Wang Xiao, Kittaka Mizuho, He Yilin, Zhang Yiwei, Ueki Yasuyoshi, Kihara Daisuke
Department of Computer Science, Purdue University, West Lafayette, IN, USA.
Department of Biomedical Sciences and Comprehensive Care, Indiana University School of Dentistry, Indianapolis, IN, USA.
Front Bioinform. 2022;2. doi: 10.3389/fbinf.2022.819570. Epub 2022 Mar 25.
Osteoclasts are multinucleated cells that exclusively resorb bone matrix proteins and minerals on the bone surface. They differentiate from monocyte/macrophage-lineage cells in the presence of osteoclastogenic cytokines such as the receptor activator of nuclear factor-κB ligand (RANKL) and are stained positive for tartrate-resistant acid phosphatase (TRAP). In vitro, osteoclast formation assays are commonly used to assess the capacity of osteoclast precursor cells for differentiating into osteoclasts wherein the number of TRAP-positive multinucleated cells are counted as osteoclasts. Osteoclasts are manually identified on cell culture dishes by human eyes, which is a labor-intensive process. Moreover, the manual procedure is not objective and result in lack of reproducibility. To accelerate the process and reduce the workload for counting the number of osteoclasts, we developed OC_Finder, a fully automated system for identifying osteoclasts in microscopic images. OC_Finder consists of cell image segmentation with a watershed algorithm and cell classification using deep learning. OC_Finder detected osteoclasts differentiated from wild-type and precursor cells at a 99.4% accuracy for segmentation and at a 98.1% accuracy for classification. The number of osteoclasts classified by OC_Finder was at the same accuracy level with manual counting by a human expert. OC_Finder also showed consistent performance on additional datasets collected with different microscopes with different settings by a different operator. Together, successful development of OC_Finder suggests that deep learning is a useful tool to perform prompt and accurate unbiased classification and detection of specific cell types in microscopic images.
破骨细胞是多核细胞,专门在骨表面吸收骨基质蛋白和矿物质。它们在破骨细胞生成细胞因子如核因子κB受体活化因子配体(RANKL)存在的情况下,从单核细胞/巨噬细胞系细胞分化而来,并对抗酒石酸酸性磷酸酶(TRAP)呈阳性染色。在体外,破骨细胞形成试验通常用于评估破骨细胞前体细胞分化为破骨细胞的能力,其中TRAP阳性多核细胞的数量被计为破骨细胞。破骨细胞是通过肉眼在细胞培养皿上手动识别的,这是一个劳动密集型过程。此外,手动操作不客观,缺乏可重复性。为了加快这一过程并减少破骨细胞计数的工作量,我们开发了OC_Finder,这是一种用于在显微镜图像中识别破骨细胞的全自动系统。OC_Finder由使用分水岭算法的细胞图像分割和使用深度学习的细胞分类组成。OC_Finder检测到从野生型和前体细胞分化而来的破骨细胞,分割准确率为99.4%,分类准确率为98.1%。OC_Finder分类的破骨细胞数量与人类专家手动计数的准确率相同。OC_Finder在由不同操作员使用不同设置的不同显微镜收集的其他数据集上也表现出一致的性能。总之,OC_Finder的成功开发表明,深度学习是在显微镜图像中对特定细胞类型进行快速、准确、无偏分类和检测的有用工具。