Mesenchymal–epithelial interactions in the skin

We investigated whether or not the topographic regulation of melanocyte differentiation is determined by mesenchymal–epithelial interactions via fibroblast-derived factors. The melanocyte density in palmoplantar human skin (i.e., skin on the palms and the soles) is five times lower than that found in nonpalmoplantar sites. Palmoplantar fibroblasts significantly suppressed the growth and pigmentation of melanocytes compared with nonpalmoplantar fibroblasts. Using cDNA microarray analysis, fibroblasts derived from palmoplantar skin expressed high levels of dickkopf 1 (DKK1; an inhibitor of the canonical Wnt signaling pathway), whereas nonpalmoplantar fibroblasts expressed higher levels of DKK3. Transfection studies revealed that DKK1 decreased melanocyte function, probably through β-catenin–mediated regulation of microphthalmia-associated transcription factor activity, which in turn modulates the growth and differentiation of melanocytes. Thus, our results provide a basis to explain why skin on the palms and the soles is generally hypopigmented compared with other areas of the body, and might explain why melanocytes stop migrating in the palmoplantar area during human embryogenesis.

[1]  R. Buscà,et al.  Cyclic AMP a key messenger in the regulation of skin pigmentation. , 2000, Pigment cell research.

[2]  R. Irion Aliens in the Neighborhood? , 2004, Science.

[3]  S. Regis,et al.  Analysis of the glucocerebrosidase gene and mutation profile in 144 Italian gaucher patients , 2002, Human mutation.

[4]  V. Hearing,et al.  A standardized protocol for assessing regulators of pigmentation. , 1999, Analytical biochemistry.

[5]  K. Yoshikawa,et al.  Regulation of keratin 9 in nonpalmoplantar keratinocytes by palmoplantar fibroblasts through epithelial-mesenchymal interactions. , 1999, The Journal of investigative dermatology.

[6]  Sharon A Miller,et al.  UV‐induced DNA damage and melanin content in human skin differing in racial/ethnic origin , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[7]  T. Jessell,et al.  The status of Wnt signalling regulates neural and epidermal fates in the chick embryo , 2001, Nature.

[8]  DATABASE: Heads or Tails , 2004, Science.

[9]  Yan Li,et al.  LDL-receptor-related protein 6 is a receptor for Dickkopf proteins , 2001, Nature.

[10]  U. Rüther,et al.  The Wnt antagonist Dickkopf‐1 is regulated by Bmp signaling and c‐Jun and modulates programmed cell death , 2002, The EMBO journal.

[11]  A. M. Arias Epithelial Mesenchymal Interactions in Cancer and Development , 2001, Cell.

[12]  C. Niehrs,et al.  Dickkopf-1 is a member of a new family of secreted proteins and functions in head induction , 1998, Nature.

[13]  J. Annereau,et al.  Regulation of melanocortin 1 receptor expression at the mRNA and protein levels by its natural agonist and antagonist , 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[14]  Sridhar Ramaswamy,et al.  Bcl2 Regulation by the Melanocyte Master Regulator Mitf Modulates Lineage Survival and Melanoma Cell Viability , 2002, Cell.

[15]  S. Ramaswamy,et al.  MLANA/MART1 and SILV/PMEL17/GP100 are transcriptionally regulated by MITF in melanocytes and melanoma. , 2003, The American journal of pathology.

[16]  Jiang Shou,et al.  Human Dkk-1, a gene encoding a Wnt antagonist, responds to DNA damage and its overexpression sensitizes brain tumor cells to apoptosis following alkylation damage of DNA , 2002, Oncogene.

[17]  U. Rüther,et al.  Bmp, Fgf and Wnt signalling in programmed cell death and chondrogenesis during vertebrate limb development: the role of Dickkopf-1. , 2002, The International journal of developmental biology.

[18]  R. Nusse,et al.  Developmental biology: Making head or tail of Dickkopf , 2001, Nature.

[19]  David Botstein,et al.  Diversity, topographic differentiation, and positional memory in human fibroblasts , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[20]  Sarah E. Millar,et al.  Characterization of Wnt gene expression in developing and postnatal hair follicles and identification of Wnt5a as a target of Sonic hedgehog in hair follicle morphogenesis , 2001, Mechanisms of Development.

[21]  K. Robison,et al.  Functional and structural diversity of the human Dickkopf gene family. , 1999, Gene.

[22]  T. Yamashita,et al.  Analysis of genes induced in peripheral nerve after axotomy using cDNA microarrays , 2002, Journal of neurochemistry.

[23]  Christof Niehrs,et al.  Kremen proteins are Dickkopf receptors that regulate Wnt/β-catenin signalling , 2002, Nature.

[24]  Stephen L. Lessnick,et al.  β-Catenin–induced melanoma growth requires the downstream target Microphthalmia-associated transcription factor , 2002, The Journal of Cell Biology.

[25]  R. Phipps,et al.  Fibroblast heterogeneity: existence of functionally distinct Thy 1(+) and Thy 1(-) human female reproductive tract fibroblasts. , 2001, The American journal of pathology.

[26]  M. Tachibana,et al.  MITF: a stream flowing for pigment cells. , 2000, Pigment cell research.

[27]  C. Clarke,et al.  Spontaneous abortion and fetal abnormality in subsequent pregnancy. , 1978, British medical journal.

[28]  D. Raible,et al.  Environmental signals and cell fate specification in premigratory neural crest , 2000, BioEssays : news and reviews in molecular, cellular and developmental biology.

[29]  E. Ziff,et al.  Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf , 2001, Mechanisms of Development.

[30]  C. Erickson,et al.  Neural crest development: the interplay between morphogenesis and cell differentiation. , 1998, Current topics in developmental biology.

[31]  C. Marcelle,et al.  Ectodermal Wnt Function as a Neural Crest Inducer , 2002, Science.

[32]  D. Raible,et al.  Direct regulation of nacre, a zebrafish MITF homolog required for pigment cell formation, by the Wnt pathway. , 2000, Genes & development.

[33]  Kazuhiro Takahashi,et al.  Melanocyte-specific Microphthalmia-associated Transcription Factor Isoform Activates Its Own Gene Promoter through Physical Interaction with Lymphoid-enhancing Factor 1* , 2002, The Journal of Biological Chemistry.

[34]  V. Ferrans,et al.  Production of melanocyte-specific antibodies to human melanosomal proteins: expression patterns in normal human skin and in cutaneous pigmented lesions. , 2001, Pigment cell research.

[35]  Y. Tsuji,et al.  Selective down-regulation of tyrosinase family gene TYRP1 by inhibition of the activity of melanocyte transcription factor, MITF. , 2002, Nucleic acids research.

[36]  Christof Niehrs,et al.  Kremen proteins are Dickkopf receptors that regulate Wnt/beta-catenin signalling. , 2002, Nature.

[37]  James A. Vaught,et al.  microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family. , 1994, Genes & development.

[38]  J. Jorcano,et al.  Cytokeratin No. 9, an epidermal type I keratin characteristic of a special program of keratinocyte differentiation displaying body site specificity , 1986, The Journal of cell biology.

[39]  G. Szabó,et al.  The Number of Melanocytes in Human Epidermis , 1954, British medical journal.

[40]  R. Krumlauf,et al.  Role of the Isthmus and FGFs in Resolving the Paradox of Neural Crest Plasticity and Prepatterning , 2002, Science.

[41]  K. Yoshikawa,et al.  Cutaneous Wound Healing: An Update , 2001, The Journal of dermatology.

[42]  B. Schaffhauser,et al.  Epithelial Mesenchymal Transition by C-Fos Estrogen Receptor Activation Involves Nuclear Translocation of β-Catenin and Upregulation of β-Catenin/Lymphoid Enhancer Binding Factor-1 Transcriptional Activity , 2000, The Journal of cell biology.

[43]  S. Shibahara,et al.  Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene , 1995, Molecular and cellular biology.

[44]  V. Swope,et al.  Long-term proliferation of human melanocytes is supported by the physiologic mitogens alpha-melanotropin, endothelin-1, and basic fibroblast growth factor. , 1995, Experimental cell research.

[45]  M. Kraus,et al.  Isolation and Biochemical Characterization of the Human Dkk-1 Homologue, a Novel Inhibitor of Mammalian Wnt Signaling* , 1999, The Journal of Biological Chemistry.

[46]  J. Taipale,et al.  The Hedgehog and Wnt signalling pathways in cancer , 2001, Nature.

[47]  Yoshiaki Kawano,et al.  Secreted antagonists of the Wnt signalling pathway , 2003, Journal of Cell Science.

[48]  M. Udey,et al.  Characterization of Wnt gene expression in murine skin: possible involvement of epidermis-derived Wnt-4 in cutaneous epithelial-mesenchymal interactions. , 1998, Experimental cell research.

[49]  Kazuhiro Takahashi,et al.  Induction of Melanocyte-specific Microphthalmia-associated Transcription Factor by Wnt-3a* , 2000, The Journal of Biological Chemistry.

[50]  F. Zhan,et al.  The role of the Wnt-signaling antagonist DKK1 in the development of osteolytic lesions in multiple myeloma. , 2003, The New England journal of medicine.

[51]  C. Niehrs,et al.  Dickkopf1 and the Spemann-Mangold head organizer. , 2001, The International journal of developmental biology.

[52]  Hosoon Choi,et al.  Wnt-5a inhibits the canonical Wnt pathway by promoting GSK-3–independent β-catenin degradation , 2003, The Journal of cell biology.

[53]  V. Hearing,et al.  Reconstituted 3-dimensional human skin of various ethnic origins as an in vitro model for studies of pigmentation. , 2003, Analytical biochemistry.

[54]  V. Hearing,et al.  Stimulation of melanoblast pigmentation by 8-methoxypsoralen:the involvement of microphthalmia-associated transcription factor, the protein kinase a signal pathway, and proteasome-mediated degradation. , 2002, The Journal of investigative dermatology.

[55]  L. Wolpert Developmental Biology , 1968, Nature.

[56]  K. Devriendt,et al.  Human piebaldism: six novel mutations of the proto‐oncogene KIT , 2002, Human mutation.

[57]  J. I. Izpisúa Belmonte,et al.  Dickkopf1 is required for embryonic head induction and limb morphogenesis in the mouse. , 2001, Developmental cell.

[58]  R. Moon,et al.  Dishevelled activates Ca2+ flux, PKC, and CamKII in vertebrate embryos , 2003, The Journal of cell biology.

[59]  Kazuhiro Takahashi,et al.  Microphthalmia‐associated transcription factor interacts with LEF‐1, a mediator of Wnt signaling , 2002, The EMBO journal.

[60]  V. Falanga,et al.  Lack of co-ordinate expression of the alpha1(I) and alpha1(III) procollagen genes in fibroblast clonal cultures. , 2000, The British journal of dermatology.

[61]  D. Fisher,et al.  Ser298 of MITF, a mutation site in Waardenburg syndrome type 2, is a phosphorylation site with functional significance. , 2000, Human molecular genetics.

[62]  A. M. Arias,et al.  Wnt signalling: pathway or network? , 1999, Current opinion in genetics & development.

[63]  D. Prockop,et al.  The Wnt Signaling Inhibitor Dickkopf-1 Is Required for Reentry into the Cell Cycle of Human Adult Stem Cells from Bone Marrow* , 2003, Journal of Biological Chemistry.

[64]  S. Shibahara,et al.  A big gene linked to small eyes encodes multiple Mitf isoforms: many promoters make light work. , 1998, Pigment cell research.

[65]  W. Pavan,et al.  Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor. , 1997, Development.

[66]  R. Page,et al.  Heterogeneity of normal human diploid fibroblasts: isolation and characterization of one phenotype. , 1984, Science.

[67]  N. Fusenig,et al.  c-Jun and JunB Antagonistically Control Cytokine-Regulated Mesenchymal–Epidermal Interaction in Skin , 2000, Cell.

[68]  S. Millar,et al.  WNT signals are required for the initiation of hair follicle development. , 2002, Developmental cell.

[69]  L. Zhou,et al.  Lack of co‐ordinate expression of the α1(I) and α1(III) procollagen genes in fibroblast clonal cultures , 2000 .

[70]  R. Spritz Piebaldism, Waardenburg syndrome, and related disorders of melanocyte development. , 1997, Seminars in cutaneous medicine and surgery.