<abstract xmlns="http://www.w3.org/1999/xhtml"> Background: Human epidermal keratinocytes (HEKs) cover the outer layer of the skin and play a key role in wound repair. Although the methods for isolation and cultivation of primary HEKs from epidermis have been used successfully in both laboratory and clinical settings, the ability to subculture (passage) these cells has yet to be established and is the primary factor hindering their usage.Objectives: We conducted this study to identify optimal subculture conditions for HEKs.Methods: We first harvested the primary HEKs from prepuce tissue specimens, and then compared three different reagent compositions (0.25% trypsin, 0.25% trypsin plus 0.01% EDTA, and 0.25% dispase digestion solution) for various periods of time at 4°C with the conventional 0.25% trypsin or 0.25% trypsin plus 0.01% EDTA digestion at room temperature.Results: Our data indicated that the cold digestion conditions yielded higher cell numbers and more viable cells than the conventional methods. Furthermore, the subcultured HEKs also adhered and grew better after four hours of a 0.25% trypsin cold digestion or after six hours of a 0.25% dispase cold digestion. These procedures produced higher numbers of HEK passages than that commonly seen experienced with conventional methods.Conclusion: The data from the current study demonstrated that the optimal subculture condition for passaging and growing HEKs in vitro is four hours digestion with 0.25% trypsin.</abstract>

Background: Human epidermal keratinocytes (HEKs) cover the outer layer of the skin and play a key role in wound repair. Although the methods for isolation and cultivation of primary HEKs from epidermis have been used successfully in both laboratory and clinical settings, the ability to subculture (passage) these cells has yet to be established and is the primary factor hindering their usage.Objectives: We conducted this study to identify optimal subculture conditions for HEKs.Methods: We first harvested the primary HEKs from prepuce tissue specimens, and then compared three different reagent compositions (0.25% trypsin, 0.25% trypsin plus 0.01% EDTA, and 0.25% dispase digestion solution) for various periods of time at 4°C with the conventional 0.25% trypsin or 0.25% trypsin plus 0.01% EDTA digestion at room temperature.Results: Our data indicated that the cold digestion conditions yielded higher cell numbers and more viable cells than the conventional methods. Furthermore, the subcultured HEKs also adhered and grew better after four hours of a 0.25% trypsin cold digestion or after six hours of a 0.25% dispase cold digestion. These procedures produced higher numbers of HEK passages than that commonly seen experienced with conventional methods.Conclusion: The data from the current study demonstrated that the optimal subculture condition for passaging and growing HEKs in vitro is four hours digestion with 0.25% trypsin.

Optimal subculture methods for passaging and growing human epidermal keratinocytes

Department of Dermatology, Third affiliated hospital of Third Military Medical University, Research Institute of wound healing and tissue engineering of Chongqing, Chongqing 400042,

Asian Biomedicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Background: Human epidermal keratinocytes (HEKs) cover the outer layer of the skin and play a key role in wound repair. Although the methods for isolation and...

Optimal subculture methods for passaging and growing human epidermal keratinocytes

Article Category: Original article

Publicado en línea: 04 feb 2017

Páginas: 635 - 641

DOI: https://doi.org/10.5372/1905-7415.0505.084

Palabras clave
Cell subculture, cold digestion, culture conditions, HEKs, human epidermal keratinocytes

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Optimal subculture methods for passaging and growing human epidermal keratinocytes

Article Category: Original article

Publicado en línea: 04 feb 2017

Páginas: 635 - 641

DOI: https://doi.org/10.5372/1905-7415.0505.084

Palabras claveCell subculture, cold digestion, culture conditions, HEKs, human epidermal keratinocytes

© 2017

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.

Palabras clave
Cell subculture, cold digestion, culture conditions, HEKs, human epidermal keratinocytes