Behind the scenes of cellular organization: Quantifying spatial phenotypes of puncta structures with statistical models including random fields.

IF 2.7 3区 生物学 Q3 CELL BIOLOGY Molecular Biology of the Cell Pub Date : 2025-03-01 Epub Date: 2025-01-09 DOI:10.1091/mbc.E24-10-0461
Kyriacos Nicolaou, Josiah B Passmore, Lukas C Kapitein, Bela M Mulder, Florian Berger
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Abstract

The cellular interior is a spatially complex environment shaped by nontrivial stochastic and biophysical processes. Within this complexity, spatial organizational principles-also called spatial phenotypes-often emerge with functional implications. However, identifying and quantifying these phenotypes in the stochastic intracellular environment is challenging. To overcome this challenge for puncta, we discuss the use of inference of point-process models that link the density of points to other imaged structures and a random field that captures hidden processes. We apply these methods to simulated data and multiplexed immunofluorescence images of Vero E6 cells. Our analysis suggests that peroxisomes are likely to be found near the perinuclear region, overlapping with the endoplasmic reticulum, and located within a distance of 1 µm to mitochondria. Moreover, the random field captures a hidden variation of the mean density in the order of 15 µm. This length scale could provide critical information for further developing mechanistic hypotheses and models. By using spatial statistical models including random fields, we add a valuable perspective to cell biology.

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细胞组织的幕后:用包括随机场在内的统计模型定量点状结构的空间表型。
细胞内部是一个由非平凡的随机和生物物理过程形成的空间复杂环境。在这种复杂性中,空间组织原则(也称为空间表型)经常与功能含义一起出现。然而,在随机细胞内环境中识别和量化这些表型是具有挑战性的。为了克服点的这一挑战,我们讨论了点过程模型的推理,该模型将点的密度与其他图像结构和捕获隐藏过程的随机场联系起来。我们将这些方法应用于Vero E6细胞的模拟数据和多路免疫荧光图像。我们的分析表明,过氧化物酶体可能位于核周区域附近,与内质网重叠,位于距离线粒体1 μm的范围内。此外,随机场捕获了平均密度在15 μm量级的隐藏变化。这种长度尺度可以为进一步发展机制假设和模型提供关键信息。通过使用包括随机场在内的空间统计模型,我们为细胞生物学增加了一个有价值的视角。
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来源期刊
Molecular Biology of the Cell
Molecular Biology of the Cell 生物-细胞生物学
CiteScore
6.00
自引率
6.10%
发文量
402
审稿时长
2 months
期刊介绍: MBoC publishes research articles that present conceptual advances of broad interest and significance within all areas of cell, molecular, and developmental biology. We welcome manuscripts that describe advances with applications across topics including but not limited to: cell growth and division; nuclear and cytoskeletal processes; membrane trafficking and autophagy; organelle biology; quantitative cell biology; physical cell biology and mechanobiology; cell signaling; stem cell biology and development; cancer biology; cellular immunology and microbial pathogenesis; cellular neurobiology; prokaryotic cell biology; and cell biology of disease.
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