Transfection of a variety of cell lines with HERV-W env induced cellular fusion that was reduced when the cell

cultures were treated with an antibody against the HERV-W Env protein.21,26 In addition, induction of fusion of BeWo cells (a human trophoblastic choriocarcinoma cell line) by forskolin was associated with increased expression of syncytin.21 Moreover, inhibition of syncytin 1 expression in primary trophoblast cells reduced the number and size of syncytia formed during culture.30 The Env glycoprotein of HERV-FRD, termed syncytin 2, is structurally similar to syncytin 1 (see Fig. 2); however, it entered the primate genome before the split of the New World and the Old World Monkeys more than 40 million years ago, while syncytin

1 entered the primate genome approximately 25 millions DNA Damage inhibitor years ago and is not present in Old World Monkeys.31 Syncytin 2 also elicits cell fusion when transiently transfected into several different cell lines.32 Interestingly, the two syncytins display different properties as both are fusogenic, but syncytin 2 has immunosuppressive properties unlike syncytin 1.33 The Env protein of ERV3 is also present in syncytiotrophoblasts and was the first ERV Env for which a potential physiological function was described.34 Although it has a long open reading frame, the protein is prematurely terminated by the presence of a stop codon in the transmembrane region (Fig. 2),

which truncates the hydrophobic domain that is required for anchoring to the Bortezomib cost cell membrane.35 It also lacks a leader and a fusion peptide and, although it harbors a region with the characteristics of an immunosuppressive domain, its function is likely diminished by the lack of membrane anchorage.36 ERV3 Env does not elicit cell fusion, although its expression increases in BeWo cells treated with forskolin. When ERV3 Env is stably expressed in undifferentiated BeWo cells, it induces changes characteristic of trophoblast differentiation, such as increased levels of chorionic gonadotropin, growth inhibition, and altered morphology.37 Considering that the ERV3 Env is expressed in a variety of normal tissues heptaminol and particularly in hormone-producing organs, including adrenal and sebaceous glands and testis, it may play a general role in hormone production.36 However, 1% of 150 healthy Caucasian individuals were found to be homozygous for a premature stop codon that would theoretically result in a severely truncated non-functional protein;38 thus, it is debatable whether the ERV3 Env has a critical biological function. Two murine ERV env genes, syncytin-A (Gm52) and syncytin-B (D930020E02Rik), were identified and found to be expressed in the syncytiotrophoblast component of the labyrinthine zone of the mouse placenta.20 Both are highly fusogenic in transfection assays.