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细胞组织的幕后故事:使用包括随机场在内的统计模型量化点状结构的空间表型。

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

作者信息

Nicolaou Kyriacos, Passmore Josiah B, Kapitein Lukas C, Mulder Bela M, Berger Florian

机构信息

Cell Biology, Neurobiology and Biophysics, Department of Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, The Netherlands.

Centre for Complex Systems Studies, Utrecht University, 3584 CE Utrecht, The Netherlands.

出版信息

Mol Biol Cell. 2025 Mar 1;36(3):ar22. doi: 10.1091/mbc.E24-10-0461. Epub 2025 Jan 9.

DOI:10.1091/mbc.E24-10-0461
PMID:39785704
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11974956/
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 m to mitochondria. Moreover, the random field captures a hidden variation of the mean density in the order of 15 m. 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.

摘要

细胞内部是一个由复杂的随机和生物物理过程塑造的空间复杂环境。在这种复杂性中,空间组织原则(也称为空间表型)常常会出现并具有功能意义。然而,在随机的细胞内环境中识别和量化这些表型具有挑战性。为了克服针对斑点的这一挑战,我们讨论了使用点过程模型的推断方法,该模型将点的密度与其他成像结构以及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重免疫荧光图像。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,并且位于距离线粒体1微米的范围内。此外,随机场捕获了平均密度约为15微米的隐藏变化。这个长度尺度可以为进一步发展机制假说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添了一个有价值的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/43a11cf0b301/mbc-36-ar22-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/e56d9ab5fd37/mbc-36-ar22-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/99cd6857a871/mbc-36-ar22-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/d40b2d369606/mbc-36-ar22-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/77c4cb694321/mbc-36-ar22-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/43a11cf0b301/mbc-36-ar22-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/e56d9ab5fd37/mbc-36-ar22-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/99cd6857a871/mbc-36-ar22-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/d40b2d369606/mbc-36-ar22-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/77c4cb694321/mbc-36-ar22-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58fa/11974956/43a11cf0b301/mbc-36-ar22-g005.jpg

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