Structural Phenotyping of Stem Cell-Derived Cardiomyocytes
Structural phenotyping based on classical image feature detection has been adopted to elucidate the molecular mechanisms behind genetically or pharmacologically induced changes in cell morphology. Here, we developed a set of 11 metrics to capture the increasing sarcomere organization that occurs int...
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Published in | Stem cell reports Vol. 4; no. 3; pp. 340 - 347 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
10.03.2015
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 2213-6711 2213-6711 |
DOI | 10.1016/j.stemcr.2015.01.020 |
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Summary: | Structural phenotyping based on classical image feature detection has been adopted to elucidate the molecular mechanisms behind genetically or pharmacologically induced changes in cell morphology. Here, we developed a set of 11 metrics to capture the increasing sarcomere organization that occurs intracellularly during striated muscle cell development. To test our metrics, we analyzed the localization of the contractile protein α-actinin in a variety of primary and stem-cell derived cardiomyocytes. Further, we combined these metrics with data mining algorithms to unbiasedly score the phenotypic maturity of human-induced pluripotent stem cell-derived cardiomyocytes.
•Image processing metrics for characterizing the contractile cytoskeleton•Unbiased data mining strategies to assess cardiomyocyte maturation•Structural phenotyping of stem cell-derived cardiomyocytes
In this article, Parker and colleagues develop metrics to quantitatively characterize myofibrillogenesis and sarcomerogenesis, the processes by which striated muscle cells assemble their contractile cytoskeleton. Further, they coupled these metrics with machine-learning algorithms to unbiasedly score the phenotypic maturity of primary and stem cell-derived cardiomyocytes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2213-6711 2213-6711 |
DOI: | 10.1016/j.stemcr.2015.01.020 |