Craniofacial Diseases Caused by Defects in Intracellular Trafficking

Genes (Basel). 2021 May 13;12(5):726. doi: 10.3390/genes12050726.

Abstract

Cells use membrane-bound carriers to transport cargo molecules like membrane proteins and soluble proteins, to their destinations. Many signaling receptors and ligands are synthesized in the endoplasmic reticulum and are transported to their destinations through intracellular trafficking pathways. Some of the signaling molecules play a critical role in craniofacial morphogenesis. Not surprisingly, variants in the genes encoding intracellular trafficking machinery can cause craniofacial diseases. Despite the fundamental importance of the trafficking pathways in craniofacial morphogenesis, relatively less emphasis is placed on this topic, thus far. Here, we describe craniofacial diseases caused by lesions in the intracellular trafficking machinery and possible treatment strategies for such diseases.

Keywords: craniofacial diseases; endocytosis; endosome/lysosome targeting; intracellular trafficking; secretory pathway.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Craniofacial Abnormalities / genetics*
  • Craniofacial Abnormalities / metabolism
  • Humans
  • Protein Transport
  • Secretory Pathway
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism*

Substances

  • Vesicular Transport Proteins