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The control of epidermal stem cells (holoclones) in the treatment of massive full-thickness burns with autologous keratinocytes cultured on fibrin.

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TLDR
In this article, the authors show that if new keratinocyte culture technologies and/or delivery systems are proposed, a careful evaluation of epidermal stem cell preservation is essential for the clinical performance of this lifesaving technology.
Abstract
Background. Cell therapy is an emerging therapeutic strategy aimed at replacing or repairing severely damaged tissues with cultured cells. Epidermal regeneration obtained with autologous cultured keratinocytes (cultured autografts) can be life-saving for patients suffering from massive full-thickness burns. However, the widespread use of cultured autografts has been hampered by poor clinical results that have been consistently reported by different burn units, even when cells were applied on properly prepared wound beds. This might arise from the depletion of epidermal stem cells (holoclones) in culture. Depletion of holoclones can occur because of (i) incorrect culture conditions, (ii) environmental damage of the exposed basal layer of cultured grafts, or (iii) use of new substrates or culture technologies not pretested for holoclone preservation. The aim of this study was to show that, if new keratinocyte culture technologies and/or "delivery systems" are proposed, a careful evaluation of epidermal stem cell preservation is essential for the clinical performance of this lifesaving technology.

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Citations
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Journal ArticleDOI

p63 identifies keratinocyte stem cells

TL;DR: It is shown by clonal analysis that p63 is abundantly expressed by epidermal and limbal holoclones, but is undetectable in paraclones, and will be of practical importance for the clinical application of epithelial cultures in cell therapy as well as for studies on epithelial tumorigenesis.
Journal ArticleDOI

Morphogenesis and Renewal of Hair Follicles from Adult Multipotent Stem Cells

TL;DR: The results indicate that the clonogenic keratinocytes are closely related, if not identical, to the multipotent stem cells, and that the regulation of whisker growth necessitates a precise control of stem cell trafficking.
Journal ArticleDOI

Limbal stem-cell therapy and long-term corneal regeneration

TL;DR: Culture of limbal stem cells represent a source of cells for transplantation in the treatment of destruction of the human cornea due to burns and success--that is, the generation of normal epithelium on donor stroma--was associated with the percentage of p63-bright holoclone-forming stem cells in culture.
Journal ArticleDOI

Stem cells in tissue engineering.

TL;DR: The identification and isolation of stem cells from a number of tissues provides appropriate targets for prospective gene therapies and has the potential to significantly alter the perspective of tissue engineering.
Journal ArticleDOI

Epidermal stem cells of the skin.

TL;DR: This work discusses the fundamental characteristics of epidermal SCs of the adult skin, the methods recently designed to isolate these cells, the genes preferentially expressed in the multipotent SC niche, and the signaling pathways involved in SC niche formation, SC maintenance, and activation.
References
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Journal ArticleDOI

Serial cultivation of strains of human epidermal keratinocytes: the formation of keratinizing colonies from single cells.

TL;DR: Human diploid epidermis epidermal cells have been successfully grown in serial culture and it is possible to isolate keratinocyte clones free of viable fibroblasts, and human diploids keratinocytes appear to have a finite culture lifetime.
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Existence of slow-cycling limbal epithelial basal cells that can be preferentially stimulated to proliferate: implications on epithelial stem cells.

TL;DR: Using 3H-thymidine labeling, a subpopulation of corneal epithelial basal cells are identified in the peripheral cornea in a region called limbus that are normally slow cycling, but can be stimulated to proliferate in response to wounding and to a tumor promotor, TPA.
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Long-term restoration of damaged corneal surfaces with autologous cultivated corneal epithelium

TL;DR: It is shown that corneal progenitor cells are localised in the limbus, that cultured limbal cells generate cohesive sheets of authentic cornean epithelium, and that autologous cultured corneals restored the corNEal surface of two patients with complete loss of the Corneal-limbus epithelio.
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Three clonal types of keratinocyte with different capacities for multiplication

TL;DR: Colony-forming human epidermal cells are heterogeneous in their capacity for sustained growth and the incidence of the different clonal types is affected by aging, since cells originating from the epidermis of older donors give rise to a lower proportion of holoclones and a higher proportion of paraclones.
Journal ArticleDOI

Growth of cultured human epidermal cells into multiple epithelia suitable for grafting.

TL;DR: It will be shown here that large amounts of cultured epithelium can be generated from a small piece of epidermis in a short time.
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