Raymond Michael J, Ray Poulomi, Kaur Gurleen, Singh Ajay V, Wan Leo Q
Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Biotech 2147, 110 8th Street, Troy, NY, 12180, USA.
Center for Biotechnology & Interdisciplinary Studies, Rensselaer Polytechnic Institute, 110 8th Street, Troy, NY, 12180, USA.
Ann Biomed Eng. 2016 May;44(5):1475-86. doi: 10.1007/s10439-015-1431-3. Epub 2015 Aug 21.
Left-right (LR) asymmetry is a biologically conserved property in living organisms that can be observed in the asymmetrical arrangement of organs and tissues and in tissue morphogenesis, such as the directional looping of the gastrointestinal tract and heart. The expression of LR asymmetry in embryonic tissues can be appreciated in biased cell alignment. Previously an in vitro chirality assay was reported by patterning multiple cells on microscale defined geometries and quantified the cell phenotype-dependent LR asymmetry, or cell chirality. However, morphology and chirality of individual cells on micropatterned surfaces has not been well characterized. Here, a Python-based algorithm was developed to identify and quantify immunofluorescence stained individual epithelial cells on multicellular patterns. This approach not only produces results similar to the image intensity gradient-based method reported previously, but also can capture properties of single cells such as area and aspect ratio. We also found that cell nuclei exhibited biased alignment. Around 35% cells were misaligned and were typically smaller and less elongated. This new imaging analysis approach is an effective tool for measuring single cell chirality inside multicellular structures and can potentially help unveil biophysical mechanisms underlying cellular chiral bias both in vitro and in vivo.
左右(LR)不对称是生物体中一种生物学上保守的特性,可在器官和组织的不对称排列以及组织形态发生过程中观察到,例如胃肠道和心脏的定向环化。胚胎组织中LR不对称的表达可通过偏向性细胞排列来体现。此前有报道称,通过在微尺度定义的几何结构上对多个细胞进行图案化处理,并对细胞表型依赖性的LR不对称性(即细胞手性)进行量化,从而建立了一种体外手性测定法。然而,微图案化表面上单个细胞的形态和手性尚未得到很好的表征。在此,开发了一种基于Python的算法,用于识别和量化多细胞图案上免疫荧光染色的单个上皮细胞。这种方法不仅产生的结果与先前报道的基于图像强度梯度的方法相似,而且还可以捕获单个细胞的特性,如面积和纵横比。我们还发现细胞核呈现出偏向性排列。约35%的细胞排列不齐,通常较小且伸长程度较低。这种新的成像分析方法是测量多细胞结构内单细胞手性的有效工具,并且有可能有助于揭示体外和体内细胞手性偏向背后的生物物理机制。