Phospholipase Cdelta1 is required for skin stem cell lineage commitment

EMBO J. 2003 Jun 16;22(12):2981-91. doi: 10.1093/emboj/cdg302.

Abstract

Phosphoinositide-specific phospholipase C (PLC) is a key enzyme in phosphoinositide turnover and is involved in a variety of physiological functions. Here we report that PLCdelta(1)-deficient mice undergo progressive hair loss in the first postnatal hair cycle. Epidermal hyperplasia was observed, and many hairs in the skin of PLCdelta(1)-deficient mice failed to penetrate the epidermis and became zigzagged owing to occlusion of the hair canal. Two major downstream signals of PLC, calcium elevation and protein kinase C activation, were impaired in the keratinocytes and skin of PLCdelta(1)-deficient mice. In addition, many cysts that had remarkable similarities to interfollicular epidermis, as well as hyperplasia of sebaceous glands, were observed. Furthermore, PLCdelta(1)-deficient mice developed spontaneous skin tumors that had characteristics of both interfollicular epidermis and sebaceous glands. From these results, we conclude that PLCdelta(1) is required for skin stem cell lineage commitment.

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cell Differentiation / physiology*
  • Cell Lineage
  • Epidermal Cells*
  • Epidermal Cyst / metabolism
  • Epidermal Cyst / pathology
  • Epidermis / pathology
  • Gene Targeting
  • Hair Diseases / genetics
  • Hair Diseases / metabolism
  • Hair Follicle / cytology
  • Hair Follicle / pathology
  • Hair Follicle / physiology
  • Humans
  • Hyperplasia
  • Isoenzymes / genetics
  • Isoenzymes / metabolism*
  • Keratinocytes / cytology
  • Keratinocytes / physiology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phospholipase C delta
  • Protein Kinase C / metabolism
  • Sebaceous Glands / cytology
  • Sebaceous Glands / metabolism
  • Sebaceous Glands / pathology
  • Signal Transduction / physiology
  • Skin / cytology*
  • Skin / growth & development
  • Skin / pathology
  • Stem Cells / physiology*
  • Type C Phospholipases / genetics
  • Type C Phospholipases / metabolism*

Substances

  • Isoenzymes
  • Protein Kinase C
  • Type C Phospholipases
  • Phospholipase C delta
  • Calcium