Chisei Ra
National Institutes of Health
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Chisei Ra.
International Archives of Allergy and Immunology | 1991
Jean-Pierre Kinet; U. Blank; Anna T. Brini; M H Jouvin; Helmut Küster; O. Mejan; Chisei Ra
The high-affinity receptor for IgE (Fc epsilon RI) on mast cells and basophils is a tetrameric complex, alpha beta gamma 2. Here we summarize the latest developments on the structure and function of this receptor. By genetic transfer, we have engineered a cell line secreting substantial amounts of a peptide containing exclusively the extracellular domain of the alpha-subunit. This domain by itself is sufficient to mediate high-affinity binding of IgE. Glycosylation and the presence of the other subunits are not necessary for the binding function. The gamma-subunit of Fc epsilon RI is part of other receptors such as Fc gamma RIII and the T cell receptor, and therefore is likely to play an important although still undefined functional role. A detailed knowledge of how the receptor interacts with IgE and induces cellular degranulation may lead to the design of new therapeutic approaches to allergic diseases. The potential strategies are discussed.
International Archives of Allergy and Immunology | 1989
Henry Metzger; Ulrich Blank; Jean-Pierre Kinet; Jarema Peter Kochan; Chisei Ra; Juan Rivera; K. White
The cDNAs for two of the subunits of the receptor with high affinity for IgE have been isolated and sequenced. That for the IgE-binding alpha subunit predicts a polypeptide with a single transmembrane segment. The predicted extracellular amino terminal portion, comprised of 180 residues, is homologous to the corresponding region of Fc gamma receptors and contains two truncated immunoglobulin-like domains. The cDNA for beta predicts a peptide with four transmembrane segments, but its sequence is unrelated to known proteins. Experiments to isolate the cDNA for the gamma subunit have begun; when completed, cotransfection of the three genes will be attempted to get expression, a process that has not so far been successful for the individual subunits. Such expression will permit further analysis of the receptors function and ultimately may provide information on how best to intervene clinically in the activation of mast cells and basophils.
Nature | 1989
Ulrich Blank; Chisei Ra; Miller L; K. White; Henry Metzger; Jean-Pierre Kinet
Nature | 1989
Chisei Ra; Marie-Hélène Jouvin; Ulrich Blank; Jean-Pierre Kinet
Journal of Biological Chemistry | 1989
Chisei Ra; Marie-Hélène Jouvin; Jean-Pierre Kinet
Nature | 1990
David G. Orloff; Chisei Ra; Stuart J. Frank; Richard D. Klausner; Jean-Pierre Kinet
Journal of Biological Chemistry | 1991
Ulrich Blank; Chisei Ra; Jean-Pierre Kinet
Proceedings of the National Academy of Sciences of the United States of America | 1988
Jean-Pierre Kinet; Ulrich Blank; Chisei Ra; K. White; Henry Metzger; Jarema Peter Kochan
European Journal of Immunology | 1989
Chisei Ra; Kiyoshi Furuichi; Juan Rivera; J. Michael Mullins; Chaviva Isersky; Kenneth N. White
European Journal of Immunology | 1990
Bosco M. C. Chan; Chisei Ra; Weining Hu; Karol D. McNeill; Hugh R. P. Miller; Dean Befus; Jean-Pierre Kinet; Arnold Froese