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Wound healing of human embryonic stem cell-derived retinal pigment epithelial cells is affected by maturation stage

BACKGROUND: Wound healing of retinal pigment epithelium (RPE) is a complex process that may take place in common age-related macular degeneration eye disease. The purpose of this study was to evaluate whether wounding and wound healing has an effect on Ca(2+) dynamics in human embryonic stem cell (h...

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Detalles Bibliográficos
Autores principales: Abu Khamidakh, Amna E., Rodriguez-Martinez, Alejandra, Kaarniranta, Kai, Kallioniemi, Anne, Skottman, Heli, Hyttinen, Jari, Juuti-Uusitalo, Kati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069779/
https://www.ncbi.nlm.nih.gov/pubmed/30064430
http://dx.doi.org/10.1186/s12938-018-0535-z
Descripción
Sumario:BACKGROUND: Wound healing of retinal pigment epithelium (RPE) is a complex process that may take place in common age-related macular degeneration eye disease. The purpose of this study was to evaluate whether wounding and wound healing has an effect on Ca(2+) dynamics in human embryonic stem cell (hESC)-RPEs cultured different periods of time. METHODS: The 9-day-cultured or 28-day-cultured hESC-RPEs from two different cell lines were wounded and the dynamics of spontaneous and mechanically induced intracellular Ca(2+) activity was measured with live-cell Ca(2+) imaging either immediately or 7 days after wounding. The healing time and speed were analyzed with time-lapse bright field microscopy. The Ca(2+) activity and healing speed were analysed with image analysis. In addition the extracellular matrix deposition was assessed with confocal microscopy. RESULTS: The Ca(2+) dynamics in hESC-RPE monolayers differed depending on the culture time: 9-day-cultured cells had higher number of cells with spontaneous Ca(2+) activity close to freshly wounded edge compared to control areas, whereas in 28-day-cultured cells there was no difference in wounded and control areas. The 28-day-cultured, wounded and 7-day-healed hESC-RPEs produced wide-spreading intercellular Ca(2+) waves upon mechanical stimulation, while in controls propagation was restricted. Most importantly, both wave spreading and spontaneous Ca(2+) activity of cells within the healed area, as well as the cell morphology of 28-day-cultured, wounded and thereafter 7-day-healed areas resembled the 9-day-cultured hESC-RPEs. CONCLUSIONS: This acquired knowledge about Ca(2+) dynamics of wounded hESC-RPE monolayers is important for understanding the dynamics of RPE wound healing, and could offer a reliable functionality test for RPE cells. The data presented in here suggests that assessment of Ca(2+) dynamics analysed with image analysis could be used as a reliable non-invasive functionality test for RPE cells. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12938-018-0535-z) contains supplementary material, which is available to authorized users.