| Literature DB >> 28742439 |
Tomoyuki Nakano1, Satoshi Ogasawara2, Toshiaki Tanaka1, Yasukazu Hozumi3, Satoru Mizuno4, Eri Satoh4, Fumio Sakane4, Naoki Okada5, Akinobu Taketomi5, Ryusuke Honma2, Takuro Nakamura6, Noriko Saidoh6, Miyuki Yanaka6, Shunsuke Itai6, Saori Handa6, Yao-Wen Chang6, Shinji Yamada6, Mika K Kaneko6, Yukinari Kato6,7, Kaoru Goto1.
Abstract
Diacylglycerol kinase (DGK) is responsible for the enzymatic conversion of diacylglycerol to phosphatidic acid. Since both diacylglycerol and phosphatidic acid serve as signaling molecules, DGK is regarded as a hub between diacylglycerol-mediated and phosphatidic acid-mediated signaling. One of the 10 DGK isozymes, DGKα, is shown to be involved in T cell function. Transfection studies using tagged expression vectors revealed that DGKα localizes to the cytoplasm and nucleus and translocates to the plasma membrane in response to T cell receptor stimulation. However, a limited number of studies reported the localization of native protein of DGKα in tissues and cells. In this study, we immunized mice with recombinant DGKα and developed several anti-DGKα monoclonal antibodies (mAbs). One of the established anti-DGKα mAbs is a clone DaMab-2 (mouse IgG1, kappa). In enzyme-linked immunosorbent assay, DaMab-2 recognized only DGKα, and did not react with the other isozymes, such as DGKγ, DGKζ, DGKη, and DGKδ. Importantly, DaMab-2 is very useful in immunocytochemical analysis of human cultured cells, indicating that DaMab-2 is advantageous to analyze the localization and function of DGKα.Entities:
Keywords: DGKα; immunocytochemical analysis; monoclonal antibody
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Year: 2017 PMID: 28742439 DOI: 10.1089/mab.2017.0023
Source DB: PubMed Journal: Monoclon Antib Immunodiagn Immunother ISSN: 2167-9436