HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Review: Lutheran/B-CAM: a laminin receptor on red blood cells and in various tissues.

Abstract
The Lutheran blood group glycoprotein (Lu), also known as basal cell adhesion molecule (B-CAM), is a transmembrane receptor with five immunoglobulin-like domains in its extracellular region; it is therefore classified as a member of the immunoglobulin (Ig) gene family. Lu/B-CAM is observed not only on red blood cells, but also on a subset of muscle and epithelial cells in various tissues. Recently, several groups have reported that Lu/B-CAM is a novel receptor for laminin a5. The laminin a5 chain is a component of the laminin-511 (alpha 5 beta 1 gamma 1), -521 (alpha 5 beta 2 gamma 1), and -523 (alpha 5 beta 2 gamma 3) heterotrimers and is expressed throughout the mammalian body. We also have shown that Lu/B-CAM is co-localized with laminin alpha 5 in various tissues. Although the biological role of Lu/B-CAM remains unclear, the specific binding of Lu/B-CAM to laminin alpha 5 suggests that it plays an important role in developmental and physiological processes. It also is necessary to investigate further the interaction between Lu/B-CAM and laminin a5 in pathological processes, including sickle cell disease and cancer.
AuthorsYamato Kikkawa, Jeffrey H Miner
JournalConnective tissue research (Connect Tissue Res) Vol. 46 Issue 4-5 Pg. 193-9 ( 2005) ISSN: 0300-8207 [Print] England
PMID16546822 (Publication Type: Journal Article, Review)
Chemical References
  • BCAM protein, human
  • Cell Adhesion Molecules
  • Laminin
  • Lutheran Blood-Group System
  • Neoplasm Proteins
  • Receptors, Laminin
  • laminin alpha5
Topics
  • Anemia, Sickle Cell (genetics)
  • Animals
  • Cell Adhesion Molecules (genetics, metabolism, pharmacology)
  • Cell Membrane (metabolism)
  • Epithelial Cells (metabolism)
  • Erythrocytes (chemistry, metabolism)
  • Humans
  • Laminin (metabolism)
  • Lutheran Blood-Group System
  • Muscle Cells (metabolism)
  • Neoplasm Proteins (genetics, metabolism, pharmacology)
  • Protein Binding (physiology)
  • Protein Structure, Tertiary (physiology)
  • Receptors, Laminin (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: