HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Processing of CD109 by furin and its role in the regulation of TGF-beta signaling.

Abstract
CD109 is a glycosylphosphatidylinositol (GPI)-anchored glycoprotein, whose expression is upregulated in squamous cell carcinomas of the lung, esophagus, uterus and oral cavity. CD109 negatively regulates transforming growth factor (TGF)-beta signaling in keratinocytes by directly modulating receptor activity. In this study, we further characterized CD109 regulation of TGF-beta signaling and cell proliferation. We found that CD109 is produced as a 205 kDa glycoprotein, which is then processed in the Golgi apparatus into 180 kDa and 25 kDa proteins by furin (furinase). 180 kDa CD109 associated with GPI-anchored 25 kDa CD109 on the cell surface and was also secreted into the culture medium. To investigate whether furinase cleavage of CD109 is necessary for its biological activity, we mutated arginine 1273 in the CD109 furinase cleavage motif (amino acid 1270-RRRR-1273) to serine (R1273S). Interestingly, CD109 R1273S neither significantly impaired TGF-beta signaling nor affected TGF-beta-mediated suppression of cell growth, although it was expressed on the cell surface as a 205 kDa protein. Consistent with this finding, the 180 kDa and 25 kDa CD109 complex, but not CD109 R1273S, associated with the type I TGF-beta receptor. These findings indicate that processing of CD109 into 180 kDa and 25 kDa proteins by furin, followed by complex formation with the type I TGF-beta receptor is required for the regulation of TGF-beta signaling in cancer cells and keratinocytes.
AuthorsS Hagiwara, Y Murakumo, S Mii, T Shigetomi, N Yamamoto, H Furue, M Ueda, M Takahashi
JournalOncogene (Oncogene) Vol. 29 Issue 15 Pg. 2181-91 (Apr 15 2010) ISSN: 1476-5594 [Electronic] England
PMID20101215 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antibodies
  • Antigens, CD
  • CD109 protein, human
  • Culture Media
  • Epitopes
  • GPI-Linked Proteins
  • Glycoproteins
  • Neoplasm Proteins
  • Smad Proteins
  • Transforming Growth Factor beta
  • Furin
Topics
  • Animals
  • Antibodies (immunology)
  • Antigens, CD (biosynthesis, chemistry, immunology, metabolism)
  • Cell Line
  • Cell Membrane (metabolism)
  • Cell Proliferation
  • Culture Media (metabolism)
  • Epitopes (immunology)
  • Furin (metabolism)
  • GPI-Linked Proteins
  • Glycoproteins (biosynthesis, chemistry, immunology, metabolism)
  • Glycosylation
  • Golgi Apparatus (metabolism)
  • Humans
  • Molecular Weight
  • Neoplasm Proteins (biosynthesis, chemistry, immunology, metabolism)
  • Neoplasms (pathology)
  • Protein Transport
  • Signal Transduction
  • Smad Proteins (metabolism)
  • Solubility
  • Transforming Growth Factor beta (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: