钙调节多头绒泡菌皮层收缩。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Physical biology Pub Date : 2023-11-17 DOI:10.1088/1478-3975/ad0a9a
Bjoern Kscheschinski, Mirna Kramar, Karen Alim
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引用次数: 0

摘要

形成管状网络的黏液型多头绒泡菌能够维持由肌动球蛋白皮层驱动的长尺度收缩模式。网络中产生的穿梭流对于生物体响应外部刺激和重组其体重产生复杂行为至关重要。然而,自组织流型的化学基础尚未完全了解。在这里,我们介绍了在简单形态的绒泡网络中游离细胞内钙的比例测量。游离钙浓度的时空格局与管半径呈近反相关关系,提示钙确实是肌动球蛋白活性的关键调节因子。我们将实验观察到的半径和钙浓度之间的相关系与包括钙作为抑制剂的理论模型的预测进行了比较。该模型的数值模拟表明,钙确实抑制绒泡菌的收缩,尽管与实验测量的相关系存在定量差异。解开收缩模式背后的机制是进一步深入了解绒泡菌复杂行为原理的关键一步。
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Calcium regulates cortex contraction inPhysarum polycephalum.

The tubular network-forming slime moldPhysarum polycephalumis able to maintain long-scale contraction patterns driven by an actomyosin cortex. The resulting shuttle streaming in the network is crucial for the organism to respond to external stimuli and reorganize its body mass giving rise to complex behaviors. However, the chemical basis of the self-organized flow pattern is not fully understood. Here, we present ratiometric measurements of free intracellular calcium in simple morphologies ofPhysarumnetworks. The spatiotemporal patterns of the free calcium concentration reveal a nearly anti-correlated relation to the tube radius, suggesting that calcium is indeed a key regulator of the actomyosin activity. We compare the experimentally observed phase relation between the radius and the calcium concentration to the predictions of a theoretical model including calcium as an inhibitor. Numerical simulations of the model suggest that calcium indeed inhibits the contractions inPhysarum, although a quantitative difference to the experimentally measured phase relation remains. Unraveling the mechanism underlying the contraction patterns is a key step in gaining further insight into the principles ofPhysarum's complex behavior.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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