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Effect of the Scaffold Microenvironment on Cell Polarizability and Capacitance Determined by Probabilistic Computations

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Journal Biomed Mater
Date 2017 Oct 27
PMID 29072579
Citations 2
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Abstract

In living systems, it is frequently stated that form follows function by virtue of evolutionary pressures on organism development, but in the study of how functions emerge at the cellular level, function often follows form. We study this chicken versus egg problem of emergent structure-property relationships in living systems in the context of primary human bone marrow stromal cells cultured in a variety of microenvironments that have been shown to cause distinct patterns of cell function and differentiation. Through analysis of a publicly available catalog of three-dimensional (3D) cell shape data, we introduce a family of metrics to characterize the 'form' of the cell populations that emerge from a variety of diverse microenvironments. In particular, measures of form are considered that are expected to have direct significance for cell function, signaling and metabolic activity: dimensionality, polarizability and capacitance. Dimensionality was assessed by an intrinsic measure of cell shape obtained from the polarizability tensor. This tensor defines ellipsoids for arbitrary cell shapes and the thinnest dimension of these ellipsoids, P , defines a reference minimal scale for cells cultured in a 3D microenvironment. Polarizability governs the electric field generated by a cell, and determines the cell's ability to detect electric fields. Capacitance controls the shape dependence of the rate at which diffusing molecules contact the surface of the cell, and this has great significance for inter-cellular signaling. These results invite new approaches for designing scaffolds which explicitly direct cell dimensionality, polarizability and capacitance to guide the emergence of new cell functions derived from the acquired form.

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References
1.
Borgens R, VANABLE Jr J, Jaffe L . Bioelectricity and regeneration: large currents leave the stumps of regenerating newt limbs. Proc Natl Acad Sci U S A. 1977; 74(10):4528-32. PMC: 431978. DOI: 10.1073/pnas.74.10.4528. View

2.
Mendicino M, Bailey A, Wonnacott K, Puri R, Bauer S . MSC-based product characterization for clinical trials: an FDA perspective. Cell Stem Cell. 2014; 14(2):141-5. DOI: 10.1016/j.stem.2014.01.013. View

3.
Chen C, Mrksich M, Huang S, Whitesides G, Ingber D . Geometric control of cell life and death. Science. 1997; 276(5317):1425-8. DOI: 10.1126/science.276.5317.1425. View

4.
Berg H, PURCELL E . Physics of chemoreception. Biophys J. 1977; 20(2):193-219. PMC: 1473391. DOI: 10.1016/S0006-3495(77)85544-6. View

5.
Liao S, Nguyen L, Ngiam M, Wang C, Cheng Z, Chan C . Biomimetic nanocomposites to control osteogenic differentiation of human mesenchymal stem cells. Adv Healthc Mater. 2014; 3(5):737-51. DOI: 10.1002/adhm.201300207. View