Dr Andrew E. Ekpenyong

Associate Professor of Physics. BPhil (Rome), BD (Rome), MS (Physics, Creighton, USA), PhD (Physics, Cambridge, UK)



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Dr Andrew Edet Ekpenyong

Associate Professor of Physics


Curriculum vitae



Office Phone: +14022802208


Physics

Creighton University

2500 California Plaza,
Omaha,
NE 68178,
USA




Dr Andrew E. Ekpenyong

Associate Professor of Physics. BPhil (Rome), BD (Rome), MS (Physics, Creighton, USA), PhD (Physics, Cambridge, UK)



Office Phone: +14022802208


Physics

Creighton University

2500 California Plaza,
Omaha,
NE 68178,
USA



Quantifying cellular differentiation by physical phenotype using digital holographic microscopy.


Journal article


K. Chalut, Andrew E. Ekpenyong, Warren L Clegg, Isabel C Melhuish, J. Guck
Integrative Biology, 2012

Semantic Scholar DOI PubMed
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Cite

APA   Click to copy
Chalut, K., Ekpenyong, A. E., Clegg, W. L., Melhuish, I. C., & Guck, J. (2012). Quantifying cellular differentiation by physical phenotype using digital holographic microscopy. Integrative Biology.


Chicago/Turabian   Click to copy
Chalut, K., Andrew E. Ekpenyong, Warren L Clegg, Isabel C Melhuish, and J. Guck. “Quantifying Cellular Differentiation by Physical Phenotype Using Digital Holographic Microscopy.” Integrative Biology (2012).


MLA   Click to copy
Chalut, K., et al. “Quantifying Cellular Differentiation by Physical Phenotype Using Digital Holographic Microscopy.” Integrative Biology, 2012.


BibTeX   Click to copy

@article{k2012a,
  title = {Quantifying cellular differentiation by physical phenotype using digital holographic microscopy.},
  year = {2012},
  journal = {Integrative Biology},
  author = {Chalut, K. and Ekpenyong, Andrew E. and Clegg, Warren L and Melhuish, Isabel C and Guck, J.}
}

Abstract

Although the biochemical changes that occur during cell differentiation are well-known, less known is that there are significant, cell-wide physical changes that also occur. Understanding and quantifying these changes can help to better understand the process of differentiation as well as ways to monitor it. Digital holographic microscopy (DHM) is a marker-free quantitative phase microscopy technique for measuring biological processes such as cellular differentiation, alleviating the need for introduction of foreign markers. We found significant changes in subcellular structure and refractive index of differentiating myeloid precursor cells within one day of differentiation induction, and significant differences depending on the type of lineage commitment. We augmented our results by showing significant changes in the softness of myeloid precursor cell differentiation within one day using optical stretching, a laser trap-based marker-free technique. DHM and optical stretching therefore provide consequential parameterization of cellular differentiation with sensitivity otherwise difficult to achieve. Therefore, we provide a way forward to quantify and understand cell differentiation with minimal perturbation using biophotonics.


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