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Depletion of NK Cells Improves Cognitive Function in the Alzheimer Disease Mouse Model
Author(s) -
Yuanyue Zhang,
Ivan Ting Hin Fung,
Poornima Sankar,
Xiangyu Chen,
Lisa S. Robison,
LongYun Ye,
Shanti S. D’Souza,
Abigail E. Salinero,
Marcy Kuentzel,
Sridar V. Chittur,
Wenzheng Zhang,
Kristen L. Zuloaga,
Qi Yang
Publication year - 2020
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.2000037
Subject(s) - disease , cognition , function (biology) , alzheimer's disease , neuroscience , medicine , psychology , biology , microbiology and biotechnology
Despite mounting evidence suggesting the involvement of the immune system in regulating brain function, the specific role of immune and inflammatory cells in neurodegenerative diseases remain poorly understood. In this study, we report that depletion of NK cells, a type of innate lymphocytes, alleviates neuroinflammation, stimulates neurogenesis, and improves cognitive function in a triple-transgenic Alzheimer disease (AD) mouse model. NK cells in the brains of triple-transgenic AD mouse model (3xTg-AD) mice exhibited an enhanced proinflammatory profile. Depletion of NK cells by anti-NK1.1 Abs drastically improved cognitive function of 3xTg-AD mice. NK cell depletion did not affect amyloid β concentrations but enhanced neurogenesis and reduced neuroinflammation. Notably, in 3xTg-AD mice depleted of NK cells, microglia demonstrated a homeostatic-like morphology, decreased proliferative response and reduced expression of neurodestructive proinflammatory cytokines. Together, our results suggest a proinflammatory role for NK cells in 3xTg-AD mice and indicate that targeting NK cells might unlock novel strategies to combat AD.

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