HEREGULIN ACTIVATION OF EXTRACELLULAR ACIDIFICATION IN MAMMARY-CARCINOMA CELLS IS ASSOCIATED WITH EXPRESSION OF HER2 AND HER3

HER2, the erbB-2/neu proto-oncogene product, is a 185-kDa transmembrane glycoprotein related to the epidermal growth factor receptor. Overexpression of HERB was reported in several human adenocarcinomas, including mammary and ovarian carcinomas. A family of glycoproteins, the heregulin/neu differentiation factors, was characterized and implicated as the Ligands for HERS. Recently, it has been shown that HERB alone is not sufficient to reconstitute high affinity heregulin receptors and that HER3 or HER4 may be the required components of the heregulin receptors on mammary carcinoma cells (Sliwkowski, M. X., Schaefer, G., Akita, R. W., Lofgren, J. A, Fitzpatrick, V. D., Nuijens, A., Fendly, B. M., Cerione, R. A., Vandlen, R. L., and Carraway, K. L., III (1994) J. Biol. Chem. 269, 14661-14665; Plowman, G. D., Green, J. M., Culouscou, J. -M., Carlton, G. W., Rothwell, V. M., and Buckley, W. (1993) Nature 366, 473-475). Using the Cytosensor(R) to measure the extracellular acidification rate, we have examined the effects of recombinant human heregulin-alpha on three mammary carcinoma cell lines expressing HER2 (MDA-MB-453, SK-BR-3, and MCF-7), an ovarian carcinoma cell line expressing HERB (SH-OV-3), and CHO-K1 and 293-EBNA cells stably transfected with HERB. By reverse transcription polymerase chain reaction and Western blotting, we found that the breast cells also express HER3 and that the ovarian line co-expresses the HER4 message. A dramatic increase in the acidification rate was observed for the mammary carcinoma cells co-expressing high levels of HERS and HER3. In contrast, the ovarian cells expressing high levels of HERB and low levels of HER4 or CHO-K1 and 293-EBNA cells expressing HERB alone were not responsive to heregulin. When these same transfected cells were exposed to monoclonal anti-HER2 antibody followed by anti-IgG to cause aggregation of the HERB molecules, an increase in the acidification rate was observed, indicating coupling of transfected HERB to the signal transduction pathway. Transfection of HER2 into MCF-7 cells, on the other hand, gave 4-fold enhanced acidification responses. These data, together with the previously reported high affinity heregulin binding and activation of tyrosine phosphorylation in HERB and HER3 co-transfected cells support the role of HERB and HER3 as components of the heregulin receptor in breast cells.