An Epithelial-Derived, Integral Membrane, Kunitz-Type Serine Protease Inhibitor in Breast Cancer

Abstract

HAI-1 was initially identified as cognate inhibitor of matriptase, a membrane-bound serine protease. Paradoxically HAI-1 is also required for matriptase activation, a process that requires sphingosine 1-phosphate (S1P)-mediated translocation of the protease to cell-cell junctions in human mammary epithelial cells. in the current report, we further explored how HAI-1 regulates this protease. First we observed that following SIP treatment HAI-1 was co-translocated with matriptase to cell-cell junctions and that the cellular ratio of HAI-1 to matriptase was maintained during this process. However, when this ratio was changed by cell treatment with HAI-1 siRNA or anti-HAI-1 mAb M19, spontaneous activation of matriptase occurred in the absence of S1P-induced translocation; S1P-induced matriptase activation was also enhanced. These results support a role for HAI-1 in protection of cell from uncontrolled matriptase activation. We next expressed matriptase, either alone or with HAI-1 in breast cancer cells that do not endogenously express either protein. A defect in matriptase trafficking to the cell surface occurred if wild type matriptase was expressed in the absence of HAI-1; this defect appeared to result from matriptase toxicity to cells. Coexpression with matriptase of wild type HAI-I, but not HAI-I mutants altered in its Kunitz domain 1, corrected the trafficking defect. in contrast, catalytically defective matriptase mutants were normal in their trafficking in the absence of HAI-1. These results are also consistent with a role for HAI-1 to prevent inappropriate matriptase proteolytic activity during its protein synthesis and trafficking. Taken together, these results support multiple roles for HAI-1 to regulate matriptase, including its proper expression, intracellular trafficking, activation, and inhibition.

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Document Details

Document Type
Technical Report
Publication Date
Aug 01, 2005
Accession Number
ADA442974

Entities

People

  • Chen-yong Lin

Organizations

  • Georgetown University

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Blood Coagulation
  • Breast Cancer
  • Cells
  • Chemistry
  • Department Of Defense
  • Enzyme Inhibitors
  • Epithelial Cells
  • Growth Factors
  • Inhibitors
  • Integrals
  • Intercellular Junctions
  • Membranes
  • Neoplasms
  • Neutral Amino Acids
  • Proteins
  • Tissues

Fields of Study

  • Biology
  • Computer science

Readers

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  • Molecular Biology and Genetics