Development of Monoclonal Antibody PMab-269 Against California Sea Lion Podoplanin

The development of protein-specific antibodies is essential for understanding a wide variety of biological phenomena. Parasitic and viral infections and cancers are known to occur within California sea lion ( Zalophus californianus ) populations. However, sensitive and specific monoclonal antibodies...

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Veröffentlicht in:Monoclonal antibodies in immunodiagnosis and immunotherapy 2021-06, Vol.40 (3), p.124-133
Hauptverfasser: Tanaka, Tomohiro, Asano, Teizo, Sano, Masato, Takei, Junko, Hosono, Hideki, Nanamiya, Ren, Nakamura, Takuro, Yanaka, Miyuki, Harada, Hiroyuki, Fukui, Masato, Suzuki, Hiroyoshi, Uchida, Kazuyuki, Nakagawa, Takayuki, Kato, Yukinari, Kaneko, Mika K
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Sprache:eng
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Zusammenfassung:The development of protein-specific antibodies is essential for understanding a wide variety of biological phenomena. Parasitic and viral infections and cancers are known to occur within California sea lion ( Zalophus californianus ) populations. However, sensitive and specific monoclonal antibodies (mAbs) for the pathophysiological analysis of California sea lion tissues have not yet been developed. A type I transmembrane glycoprotein, podoplanin (PDPN), is a known diagnostic marker of lymphatic endothelial cells. We have previously developed several anti-PDPN mAbs in various mammalian species, with applications in flow cytometry, Western blotting, and immunohistochemistry. In this study, we established a novel mAb against California sea lion PDPN (seaPDPN), clone PMab-269 (mouse IgG 1 , kappa), using a Cell-Based Immunization and Screening method. PMab-269 is specifically detected in seaPDPN-overexpressed Chinese hamster ovary (CHO)-K1 cells using flow cytometry and Western blotting. Moreover, PMab-269 clearly identified pulmonary type I alveolar cells, renal podocytes, and colon lymphatic endothelial cells in California sea lion tissues using immunohistochemistry. These findings demonstrate the usefulness of PMab-269 for the pathophysiological analysis of lung, kidney, and lymphatic tissues of the California sea lion.
ISSN:2167-9436
2167-9436
DOI:10.1089/mab.2021.0011