Confocal microscopy analysis of native, full length and B-domain deleted coagulation factor VIII trafficking in mammalian cells

Sven Becker; Jeremy C. Simpson; Rainer Pepperkok; Stefan Heinz; Christian Herder; Manuel Grez; Erhard Seifried; Torsten Tonn

doi:10.1160/TH03-06-0360

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2004; 92(01): 23-35
DOI: 10.1160/TH03-06-0360

Blood Coagulation, Fibrinolysis and Cellular Haemostasis

Schattauer GmbH

Confocal microscopy analysis of native, full length and B-domain deleted coagulation factor VIII trafficking in mammalian cells

Authors

Sven Becker

¹Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Baden-Wuerttemberg-Hesse, Frankfurt/Main, Germany
Jeremy C. Simpson

²European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
Rainer Pepperkok

²European Molecular Biology Laboratory (EMBL), Heidelberg, Germany
Stefan Heinz

¹Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Baden-Wuerttemberg-Hesse, Frankfurt/Main, Germany
Christian Herder

¹Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Baden-Wuerttemberg-Hesse, Frankfurt/Main, Germany

³Chemotherapeutisches Forschungsinstitut Georg-Speyer Haus, Frankfurt/Main, Germany
Manuel Grez

³Chemotherapeutisches Forschungsinstitut Georg-Speyer Haus, Frankfurt/Main, Germany
Erhard Seifried

¹Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Baden-Wuerttemberg-Hesse, Frankfurt/Main, Germany
Torsten Tonn

¹Institute for Transfusion Medicine and Immunohematology, Red Cross Blood Donor Service Baden-Wuerttemberg-Hesse, Frankfurt/Main, Germany

Abstract

Summary

In mammalian cells, factor VIII (FVIII) secretion depends upon its interaction with chaperones of the endoplasmic reticulum (ER) and requires a unique ATP-dependent step to dissociate aggregates formed within the ER. To further elucidate mechanisms which might account for the inefficient secretion of recombinant FVIII (rFVIII), we have analyzed the pathways of recombinant full length (rFVIII-FL) and B-domain deleted (rFVIIIΔB) FVIII and compared these to the secretion route of native FVIII in primary hepatocytes. Using confocal laser scanning microscopy in combination with a pulse chase of a known secretion marker, we describe the trafficking route of FVIII, which upon release from the ER – where it colocalizes with calnexin – is transported to the Golgi complex in vesiculartubular transport complexes (VTCs) which could be further identified as being COP I coated. However, a large portion of rFVIII is retained in the ER and additionally in structures which could not be assigned to the ER, Golgi complex or intermediate compartment. Moderate BiP transcription levels indicate that this observed retention of FVIII does not reflect cellular stress due to an overexpression of FVIII-protein in transduced cells. Moreover, a pulse of newly synthesized rFVIII protein is released within 4 hrs, indicating that once rFVIII is released from the ER there is no further limitation to its secretion. Our data provide new details about the secretory route of FVIII, which may ultimately help to identify factors currently limiting the efficient and physiological expression of FVIII in gene therapy and manufacture.

Keywords

Coagulation - co-factors - intracellular transport - vesicular tubular carriers - COPI

Full Text

References

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