Construction of a bilayered dermal equivalent containing human papillary and reticular dermal fibroblasts: use of fluorescent vital dyes.

Bilayered dermal equivalents were constructed by seeding human papillary and reticular dermal fibroblasts into separate layers of type I collagen and allowing these layers to gel into a single entity. That these bilayered gels had fused was established through histologic examination and from the fact that these gels, when detached, contracted as a single unit. Papillary and reticular dermal fibroblasts remained in their respective layers as established by differentially labeling these dermal cells with fluorescent vital dyes l,l'-dioctacecyl-3,3,3',3'-tetramethylindocabocyanine perchlorate, DiIC(18)(3) (Dil), and 3,3'-dioctadecyloxacarbocyanine perchlorate, DiOC(18)(3) (DiO). The labeling with these vital dyes did not interfere with the ability of the cells to proliferate or to contract floating type I collagen gels. Thus, these bilayered gels can provide the means of creating dermal equivalents that contain a variety of different dermal cell types to assess their relative abilities, either alone or in various combinations, to support keratinocyte proliferation and differentiation and to contribute, eventually, to the formation of a multilayered skin equivalent.

[1]  A I Caplan,et al.  A chemically defined medium supports in vitro proliferation and maintains the osteochondral potential of rat marrow-derived mesenchymal stem cells. , 1995, Experimental cell research.

[2]  L. C. Keller,et al.  Dermal fibroblasts activate keratinocyte outgrowth on collagen gels. , 1994, Journal of cell science.

[3]  D. Roop,et al.  Retinoic acid suppression of loricrin expression in reconstituted human skin cultured at the liquid-air interface. , 1994, The Journal of investigative dermatology.

[4]  S. Yuspa,et al.  Reconstitution of hair follicle development in vivo: determination of follicle formation, hair growth, and hair quality by dermal cells. , 1993, The Journal of investigative dermatology.

[5]  B. O’Malley,et al.  DiI as a marker for cellular transplantation into solid organs. , 1992, BioTechniques.

[6]  S. Guerret,et al.  Cell migration influences collagen gel contraction. , 1992, Journal of submicroscopic cytology and pathology.

[7]  B. Rollins,et al.  Human keratinocyte growth‐promoting activity on the surface of fibroblasts , 1991, Journal of cellular physiology.

[8]  A. Malmström,et al.  Proliferation of cultured fibroblasts is inhibited by L‐Iduronate—containing glycosaminoglycans , 1991, Journal of cellular physiology.

[9]  C. Stern,et al.  The marginal zone and its contribution to the hypoblast and primitive streak of the chick embryo. , 1990, Development.

[10]  E. W. Rubel,et al.  Neuronal tracing with DiI: decalcification, cryosectioning, and photoconversion for light and electron microscopic analysis. , 1990, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[11]  S. Fraser,et al.  Pathways of trunk neural crest cell migration in the mouse embryo as revealed by vital dye labelling. , 1990, Development.

[12]  M. G. Honig,et al.  Dil and DiO: versatile fluorescent dyes for neuronal labelling and pathway tracing , 1989, Trends in Neurosciences.

[13]  E. Adachi,et al.  Growth rate of human fibroblasts is repressed by the culture within reconstituted collagen matrix but not by the culture on the matrix. , 1989, Matrix.

[14]  R. Oliver,et al.  Whisker growth induced by implantation of cultured vibrissa dermal papilla cells in the adult rat. , 1986, Journal of embryology and experimental morphology.

[15]  I. Schafer,et al.  Comparative observation of fibroblasts derived from the papillary and reticular dermis of infants and adults: Growth kinetics, packing density at confluence and surface morphology , 1985, Mechanisms of Ageing and Development.

[16]  L. Dubertret,et al.  The contractility of fibroblasts in a collagen lattice is reduced by corticosteroids. , 1984, The Journal of investigative dermatology.

[17]  E Bell,et al.  The reconstitution of living skin. , 1983, The Journal of investigative dermatology.

[18]  T. Allen,et al.  The contraction of collagen matrices by dermal fibroblasts. , 1983, Journal of ultrastructure research.

[19]  E J Holborow,et al.  Fading of immunofluorescence during microscopy: a study of the phenomenon and its remedy. , 1982, Journal of immunological methods.

[20]  E Bell,et al.  Living tissue formed in vitro and accepted as skin-equivalent tissue of full thickness. , 1981, Science.

[21]  G. Grove,et al.  Human skin fibroblasts derived from papillary and reticular dermis: differences in growth potential in vitro. , 1979, Science.

[22]  R. Oliver,et al.  Dermal cell populations show variable competence in epidermal cell support: stimulatory effects of hair papilla cells. , 1991, Journal of cell science.

[23]  F. Grinnell,et al.  Spatial regulation of fibroblast proliferation: an explanation for cell regression at the end of the wound repair. , 1991, Progress in clinical and biological research.

[24]  L. Weiss,et al.  Histology : cell and tissue biology , 1983 .

[25]  M. L. Godeau,et al.  [The skin]. , 1977, Soins; la revue de reference infirmiere.