Abstract

Epithelial glycoprotein 330 (gp330) is structurally similar to the multifunctional alpha 2-macroglobulin receptor/low density lipoprotein receptor-related protein (alpha 2MR/LRP), gp330 and alpha 2MR/LRP bind Ca2+ with high affinity, and both receptors bind and mediate endocytosis of alpha 2MR-associated protein (RAP). In the present report, we describe that affinity-purified gp330 from rabbit renal cortex binds plasminogen activator inhibitor type-1 (PAI-1) complexed with urokinase-type plasminogen activator (uPA). alpha 2M-methylamine, which binds with high affinity to alpha 2MR/LRP, did not bind to gp330. The apparent Kd for binding of uPA.PAI-1 complexes was about 0.8 nM at 4 degrees C. The binding was calcium-dependent and inhibited by recombinant RAP (rRAP) and tissue type plasminogen activator-PAI-1 complexes. Thin sections of rabbit renal proximal tubules bound 125I-labeled uPA.PAI-1 and rRAP in the apical part of proximal tubules corresponding to the localization of gp330. The binding of 125I-uPA.PAI-1 complexes in tubules was abolished by excess unlabeled rRAP, and a rRAP-inhibitable endocytosis and degradation of labeled uPA.PAI-1 complexes was demonstrated by perfusion of isolated rabbit proximal tubules. The results establish an endocytotic function of gp330 and suggest that gp330 is an important component of the fibrinolytic system in gp330-containing epithelial as found in, for example, kidney and lung.

Highlights

  • From the SZnstitute of Medical Biochemistry, TDepartment of Cell Biology,Znstitute of Anatomy, and I)Zmtituteof Molecular Biology, University of Aarhus, DK-8000Aarhus C, Denmark

  • Gp330 from rabbit renal cortex binds plasminogen ac-associated protein (RAP), inhibits the binding of a2M-protivator inhibitor type-1 (PAI-1) complexed with uro- teinase complexes (9-ll), plasminogen activator-plasminogen kinase-type plasminogen activator. azM-meth-' activator inhibitor type-1complexes (PA.PAI-1) [12,13,14] and ylamine, which bindws ith high affinity to azMR/LRP, lipoproteins [10] toa2MR/LRP

  • The binding was calcium-dependent and inhibited by recombinant RAP and tissue type plasminogen activator-PAI-1 complexes.Thinsections ofrabbit renal proximal tubules boundlZ6I-labeleduPA-PAI-1 and rRAP in the apical part of proximal tubules corresponding to the localization of gp330

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Summary

Introduction

From the SZnstitute of Medical Biochemistry, TDepartment of Cell Biology,Znstitute of Anatomy, and I)Zmtituteof Molecular Biology, University of Aarhus, DK-8000Aarhus C, Denmark. The binding of 'z61-uPA*PAI-1complexes in tubulews as abolished by excess unlabeledrRAP,and a rRAP-inhibitable immunocytochemical studies have revealed an intracellular localization [7,8,9]. Complexes was demonstrated by perfusion of isolated The present study shows a high affinity, Ca2+-dependent rabbit proximal tubules.

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