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Polyphosphate, the physiological metabolic fuel for corneal cells: a potential biomaterial for ocular surface repair

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Abstract

The regeneration of the epithelium, covering the avascular cornea, involves the processes of differentiation, proliferation and migration of cells originating from the corneal epithelial stem cells. We ask the question if these energy-consuming processes can be fueled by the physiological, inorganic polyphosphate (polyP), the main energy storage/donor molecule in the extracellular space. The ex vivo results reveal that addition of polyP, in the form of soluble Na-polyP, to the culture medium elicits a strong stimulatory effect on cell viability/growth and migration of corneal epithelial cells. Microscopic analyses of partially denuded cornea specimens show that in the presence of polyP, but not in polyP-free controls, cells are migrating centripetally from the corneal limbus towards the corneal center. In vitro experiments using human corneal epithelial cells reveal an even stronger stimulatory effect on growth rates by calcium-polyP microparticles (Ca-polyP-MP) that mimic the physiological form of polyP in the platelets compared to particle-free Na-polyP, most likely by the transformation of Ca-polyP-MP into a biologically active coacervate. The increase in cell proliferation is paralleled with an increased expression of mucin 1. Our results suggest that polyP, in the form of the water-soluble Na-polyP, has the potential to be applicable as a biomimetic tear fluid to maintain and restore the integrity of the corneal epithelium.

Graphical abstract: Polyphosphate, the physiological metabolic fuel for corneal cells: a potential biomaterial for ocular surface repair

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Publication details

The article was received on 14 Aug 2019, accepted on 21 Oct 2019 and first published on 23 Oct 2019


Article type: Paper
DOI: 10.1039/C9BM01289C
Biomater. Sci., 2019, Advance Article

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    Polyphosphate, the physiological metabolic fuel for corneal cells: a potential biomaterial for ocular surface repair

    X. Wang, A. Gericke, M. Ackermann, S. Wang, M. Neufurth, H. C. Schröder, N. Pfeiffer and W. E. G. Müller, Biomater. Sci., 2019, Advance Article , DOI: 10.1039/C9BM01289C

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