Cereblon regulates NK cell cytotoxicity and migration via Rac1 activation.
Eur J Immunol
; 51(11): 2607-2617, 2021 11.
Article
em En
| MEDLINE
| ID: mdl-34392531
ABSTRACT
Rearrangement of the actin cytoskeleton is critical for cytotoxic and immunoregulatory functions as well as migration of natural killer (NK) cells. However, dynamic reorganization of actin is a complex process, which remains largely unknown. Here, we investigated the role of the protein Cereblon (CRBN), an E3 ubiquitin ligase complex co-receptor and the primary target of the immunomodulatory drugs, in NK cells. We observed that CRBN partially colocalizes with F-actin in chemokine-treated NK cells and is recruited to the immunological synapse, thus suggesting a role for this protein in cytoskeleton reorganization. Accordingly, silencing of CRBN in NK cells results in a reduced cytotoxicity that correlates with a defect in conjugate and lytic synapse formation. Moreover, CRBN depletion significantly impairs the ability of NK cells to migrate and reduces the enhancing effect of lenalidomide on NK cell migration. Finally, we provided evidence that CRBN is required for activation of the small GTPase Rac1, a critical mediator of cytoskeleton dynamics. Indeed, in CRBN-depleted NK cells, chemokine-mediated or target cell-mediated Rac1 activation is significantly reduced. Altogether our data identify a critical role for CRBN in regulating NK cell functions and suggest that this protein may mediate the stimulatory effect of lenalidomide on NK cells.
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Texto completo:
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Base de dados:
MEDLINE
Assunto principal:
Células Matadoras Naturais
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Movimento Celular
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Proteínas rac1 de Ligação ao GTP
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Citotoxicidade Imunológica
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Ubiquitina-Proteína Ligases
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Proteínas Adaptadoras de Transdução de Sinal
Limite:
Humans
Idioma:
En
Ano de publicação:
2021
Tipo de documento:
Article