Increase in the Intracellular Bulk Water Content in the Early Phase of Cell Death of Keratinocytes, Corneoptosis, as Revealed by 65 GHz Near-Field CMOS Dielectric Sensor

Molecules. 2022 Apr 30;27(9):2886. doi: 10.3390/molecules27092886.

Abstract

While bulk water and hydration water coexist in cells to support the expression of biological macromolecules, how the dynamics of water molecules, which have long been only a minor role in molecular biology research, relate to changes in cellular states such as cell death has hardly been explored so far due to the lack of evaluation techniques. In this study, we developed a high-precision measurement system that can discriminate bulk water content changes of ±0.02% (0.2 mg/cm3) with single-cell-level spatial resolution based on a near-field CMOS dielectric sensor operating at 65 GHz. We applied this system to evaluate the temporal changes in the bulk water content during the cell death process of keratinocytes, called corneoptosis, using isolated SG1 (first layer of stratum granulosum) cells in vitro. A significant irreversible increase in the bulk water content was observed approximately 1 h before membrane disruption during corneoptosis, which starts with cytoplasmic high Ca2+ signal. These findings suggest that the calcium flux may have a role in triggering the increase in the bulk water content in SG1 cells. Thus, our near-field CMOS dielectric sensor provides a valuable tool to dissect the involvement of water molecules in the various events that occur in the cell.

Keywords: SG1 cell; bulk water content; corneoptosis; fluorescence imaging; near-field CMOS dielectric sensor.

MeSH terms

  • Cell Death
  • Epidermis / metabolism
  • Keratinocytes* / metabolism
  • Water* / metabolism

Substances

  • Water

Grants and funding

This work was financially supported by the RIKEN Special Postdoctoral Researcher Program; by RIKEN Incentive Research Projects; by JST Industry Academia Collaborative R&D; by JST PRESTO grant number JPMJPR2008; by Grant-in-Aid Scientific Research (B) grant number JP22H03; and by AMED grant numbers 19gm1010001, 18gm1010001, 19ek0410058, and 18ek0410028.