New insights into the molecular control of the lymphatic vascular system and its role in disease

J Invest Dermatol. 2006 Oct;126(10):2167-77. doi: 10.1038/sj.jid.5700464.

Abstract

The cutaneous lymphatic system plays an important role in the maintenance of tissue fluid homeostasis, in the afferent phase of the immune response, and in the metastatic spread of skin cancers. However, the lymphatic system has not received as much scientific attention as the blood vascular system, largely due to a lack of lymphatic-specific markers and to the dearth of knowledge about the molecular regulation of its development and function. The recent identification of genes that specifically control lymphatic development and the growth of lymphatic vessels (lymphangiogenesis), together with the discovery of new lymphatic endothelium-specific markers, have now provided new insights into the molecular mechanisms that control lymphatic growth and function. Moreover, studies of several genetic mouse models have set the framework for a new molecular model for embryonic lymphatic vascular development, and have identified molecular pathways whose mutational inactivation leads to human diseases associated with lymphedema. These scientific advances have also provided surprising evidence that malignant tumors can directly promote lymphangiogenesis and lymphatic metastasis, and that lymphatic vessels play a major role in cutaneous inflammation and in the cutaneous response to UVB irradiation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Chemokine CCL21
  • Chemokines, CC / physiology
  • Endothelium, Lymphatic / physiology
  • Glycoproteins / physiology
  • Humans
  • Lymphangiogenesis
  • Lymphatic Metastasis
  • Lymphatic Vessels / anatomy & histology
  • Lymphatic Vessels / embryology
  • Lymphatic Vessels / physiology*
  • Lymphedema / genetics
  • Lymphedema / therapy
  • Sarcoma, Kaposi / etiology
  • Vascular Endothelial Growth Factor C / physiology
  • Vascular Endothelial Growth Factor D / physiology
  • Vascular Endothelial Growth Factor Receptor-3 / physiology
  • Vesicular Transport Proteins

Substances

  • CCL21 protein, human
  • Ccl21c protein, mouse
  • Chemokine CCL21
  • Chemokines, CC
  • Glycoproteins
  • LYVE1 protein, human
  • Vascular Endothelial Growth Factor C
  • Vascular Endothelial Growth Factor D
  • Vesicular Transport Proteins
  • Vascular Endothelial Growth Factor Receptor-3