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Naoto Matsuki

Researcher at Vanderbilt University

Publications -  9
Citations -  2123

Naoto Matsuki is an academic researcher from Vanderbilt University. The author has contributed to research in topics: Cell & T-cell receptor. The author has an hindex of 7, co-authored 9 publications receiving 2056 citations. Previous affiliations of Naoto Matsuki include Pennsylvania State University.

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Reversible Defects in Natural Killer and Memory Cd8 T Cell Lineages in Interleukin 15–Deficient Mice

TL;DR: Critical roles for IL-15 in the development of specific lymphoid lineages are revealed and the ability to rescue lymphoid defects inIL-15−/− mice by IL- 15 administration represents a powerful means by which to further elucidate the biological roles of this cytokine.
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Distinct Roles of Dendritic Cells and B Cells in Va14Ja18 Natural T Cell Activation In Vivo

TL;DR: It is reported that dendritic cells (DC) play a critical role in αGalCer-mediated activation of iNKT cells and subsequent transactivation of NK cells, and the differential immune outcome based on the type of APC that displays glycolipid Ags in vivo has implications for the design of therapies that harness the immunoregulatory functions of inKT cells.
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Lipid Protein Interactions: The Assembly of CD1d1 with Cellular Phospholipids Occurs in the Endoplasmic Reticulum

TL;DR: It is predicted that cellular lipids occlude the hydrophobic Ag-binding groove of CD1 during assembly until they are exchanged for a glycolipid Ag(s) within the recycling compartment for display on the plasma membrane, akin to the function of invariant chain in MHC class II assembly.
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NF-κB Controls Cell Fate Specification, Survival, and Molecular Differentiation of Immunoregulatory Natural T Lymphocytes

TL;DR: It is demonstrated that antiapoptotic signals relayed by NF-κB critically control cell fate specification and molecular differentiation of iNKT cells and, hence, reveal a novel role for such signals within the immune system.
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Another View of T Cell Antigen Recognition: Cooperative Engagement of Glycolipid Antigens by Va14Ja18 Natural TCR

TL;DR: It is discovered that the Vb repertoire of iNKT cells impacts recognition and Ag avidity, and that stimulation with suboptimal avidity Ag results in preferential expansion of high-affinity iN KT cells.