EndoPDI, a Novel Protein-disulfide Isomerase-like Protein That Is Preferentially Expressed in Endothelial Cells Acts as a Stress Survival Factor

• Published in: The Journal of biological chemistry Vol. 278; no. 47; pp. 47079 - 47088
• Main Authors: Sullivan, Dianne C., Huminiecki, Lucasz, Moore, John W., Boyle, Joseph J., Poulsom, Richard, Creamer, Daniel, Barker, Jonathan, Bicknell, Roy
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 21.11.2003; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid Motifs; Amino Acid Sequence; Apoptosis; DNA, Complementary; EndoPDI protein; Endothelial Cells - enzymology; Enzyme Induction; Humans; Hypoxia - enzymology; Hypoxia - pathology; Molecular Sequence Data; Molecular Weight; Neoplasm Proteins - biosynthesis; Neoplasm Proteins - chemistry; Neoplasm Proteins - physiology; Protein Disulfide-Isomerases - biosynthesis; Protein Disulfide-Isomerases - chemistry; Protein Disulfide-Isomerases - physiology; Sequence Alignment; Thioredoxins; Tissue Distribution
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M308124200

We have identified a novel protein-disulfide isomerase and named it endothelial protein-disulfide isomerase (EndoPDI) because of its high expression in endothelial cells. Isolation of the full-length cDNA showed EndoPDI to be a 48 kDa protein that has three APWCGHC thioredoxin motifs in contrast to the two present in archetypal PDI. Ribonuclease protection and Western analysis has shown that hypoxia induces EndoPDI mRNA and protein expression. In situ hybridization analysis showed that EndoPDI expression is rare in normal tissues, except for keratinocytes of the hair bulb and syncytiotrophoblasts of the placenta, but was present in the endothelium of tumors and in other hypoxic lesions such as atherosclerotic plaques. We have compared the function of EndoPDI to that of PDI in endothelial cells using specific siRNA. PDI was shown to have a protective effect on endothelial cells under both normoxia and hypoxia. In contrast, EndoPDI has a protective effect only in endothelial cells exposed to hypoxia. The loss of EndoPDI expression under hypoxia caused a significant decrease in the secretion of adrenomedullin, endothelin-1, and CD105; molecules that protect endothelial cells from hypoxia-initiated apoptosis. The identification of an endothelial PDI further extends this increasing multigene family and EndoPDI, unlike archetypal PDI, may be a molecule with which to target tumor endothelium.