Summary of ssbd-repos-000188

SSBD:database
URL

Name
ssbd-repos-000188 (188-Ipponjima-NHEKsCornification)
URL
DOI
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Title
Images of morphological changes in granular cells during cornification.
Description
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Submited Date
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Release Date
2022-03-31
Updated Date
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License
Funding information
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File formats
Data size
265.3 GB

Organism
Homo sapiens
Strain
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Cell Line
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Genes
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Proteins
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GO Molecular Function (MF)
NA
GO Biological Process (BP)
mitochondrial depolarization, keratinocyte activation
GO Cellular Component (CC)
NA, nucleus
Study Type
Organelles, Humans, Cells, Microscopy, Cell Shape, S100 Proteins, S100 Proteins/metabolism, Cultured, Models, Keratinocytes/cytology, Keratinocytes/metabolism, Organelles/metabolism, Time-Lapse Imaging/methods, Time-Lapse Imaging, Keratinocytes, Biological, Organelles/ultrastructure, Keratinocytes/ultrastructure
Imaging Methods
time lapse microscopy, two-photon laser scanning microscopy

Method Summary
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Related paper(s)

Sari Ipponjima, Yuki Umino, Masaharu Nagayama, Mitsuhiro Denda (2020) Live imaging of alterations in cellular morphology and organelles during cornification using an epidermal equivalent model., Scientific reports, Volume 10, Number 1, pp. 5515

Published in 2020 Mar 26 (Electronic publication in March 26, 2020, midnight )

(Abstract) 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.
(MeSH Terms)

Contact(s)
Sari Ipponjima
Organization(s)
Hokkaido University , Research Center of Mathematics for Social Creativity, Research Institute for Electronic Science
Image Data Contributors
Quantitative Data Contributors

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