Figure 9.
Figure 9. Schematic representation of p97 regulation of plasminogen and cell migration. This schematic representation summarizes the results obtained for p97 in the present study. (A) The interaction of pro-uPA and plasminogen with soluble activity increases the activation of plasminogen. This induction could be inhibited by the mAb L235, which recognizes a conformational epitope on p97. (B) The addition of mAb L235 reduces the plasminolytic activity on HMEC-1 cell surface and results in an inhibition of cell migration. (C) The interaction of plasminogen and pro-uPA with membrane-bound p97 (mb p97) is diminished when exogenous, competing human recombinant p97 is added. This also caused a decrease in the activation of plasminogen (plg) and leads to an inhibition of cell migration. This representation of the interaction between p97 and pro-uPA indicates that the balance between membrane bound and soluble p97 may be crucial for cell migration.

Schematic representation of p97 regulation of plasminogen and cell migration. This schematic representation summarizes the results obtained for p97 in the present study. (A) The interaction of pro-uPA and plasminogen with soluble activity increases the activation of plasminogen. This induction could be inhibited by the mAb L235, which recognizes a conformational epitope on p97. (B) The addition of mAb L235 reduces the plasminolytic activity on HMEC-1 cell surface and results in an inhibition of cell migration. (C) The interaction of plasminogen and pro-uPA with membrane-bound p97 (mb p97) is diminished when exogenous, competing human recombinant p97 is added. This also caused a decrease in the activation of plasminogen (plg) and leads to an inhibition of cell migration. This representation of the interaction between p97 and pro-uPA indicates that the balance between membrane bound and soluble p97 may be crucial for cell migration.

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