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Live imaging of alterations in cellular morphology and organelles during cornification using an epidermal equivalent model
The stratum corneum plays a crucial role in epidermal barrier function. Various changes occur in granular cells at the uppermost stratum granulosum during cornification. To understand the temporal details of this process, we visualized the cell shape and organelles of cornifying keratinocytes in a l...
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Published in: | Scientific reports 2020-03, Vol.10 (1), p.5515-5515, Article 5515 |
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description | The stratum corneum plays a crucial role in epidermal barrier function. Various changes occur in granular cells at the uppermost stratum granulosum during cornification. To understand the temporal details of this process, we visualized the cell shape and organelles of cornifying keratinocytes in a living human epidermal equivalent model. Three-dimensional time-lapse imaging with a two-photon microscope revealed that the granular cells did not simply flatten but first temporarily expanded in thickness just before flattening during cornification. Moreover, before expansion, intracellular vesicles abruptly stopped moving, and mitochondria were depolarized. When mitochondrial morphology and quantity were assessed, granular cells with fewer, mostly punctate mitochondria tended to transition to corneocytes. Several minutes after flattening, DNA leakage from the nucleus was visualized. We also observed extension of the cell-flattening time induced by the suppression of filaggrin expression. Overall, we successfully visualized the time-course of cornification, which describes temporal relationships between alterations in the transition from granular cells to corneocytes. |
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Various changes occur in granular cells at the uppermost stratum granulosum during cornification. To understand the temporal details of this process, we visualized the cell shape and organelles of cornifying keratinocytes in a living human epidermal equivalent model. Three-dimensional time-lapse imaging with a two-photon microscope revealed that the granular cells did not simply flatten but first temporarily expanded in thickness just before flattening during cornification. Moreover, before expansion, intracellular vesicles abruptly stopped moving, and mitochondria were depolarized. When mitochondrial morphology and quantity were assessed, granular cells with fewer, mostly punctate mitochondria tended to transition to corneocytes. Several minutes after flattening, DNA leakage from the nucleus was visualized. We also observed extension of the cell-flattening time induced by the suppression of filaggrin expression. 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subjects | 631/80 631/80/642 631/80/82 Cell Shape Cell size Cells, Cultured Cytology Filaggrin Humanities and Social Sciences Humans Keratinocytes Keratinocytes - cytology Keratinocytes - metabolism Keratinocytes - ultrastructure Microscopy Mitochondria Models, Biological Morphology multidisciplinary Organelles Organelles - metabolism Organelles - ultrastructure S100 Proteins - metabolism Science Science (multidisciplinary) Stratum corneum Time-Lapse Imaging - methods |
title | Live imaging of alterations in cellular morphology and organelles during cornification using an epidermal equivalent model |
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