Bidirectional factors impact the migration of NK cells to draining lymph node in aged mice during influenza virus infection.

Abstract:

:Natural killer (NK) cells play an important role in controlling several viral diseases. Our previous studies demonstrated an age-dependent susceptibility to mousepox due to defective NK cell responses and trafficking. However, the mechanisms that underlie the age-related impairment in NK cell migration have yet to be identified. In the present study, we demonstrated that after influenza A virus (IAV) infection, NK cells from aged mice (17-19months old) failed to accumulate in draining lymph node (D-LN). We found that both environmental and intrinsic factors played roles for this defect. After infection, increase of chemokine transcripts, especially CXCL9, 10 and 11, which are important for NK cells homing to D-LN, was significantly lower in the D-LN of aged mice compared with those of young mice. Further, the expression levels of β2-integrins and β-actins, which play critical roles in NK cells homing to D-LN failed to be up-regulated in NK cells from aged mice. Finally, actin polymerization rates in NK cells from aged mice were also delayed compared to that of the young mice after IAV infection. Taken together, our data indicate that bi-directional factors play essential roles in the defective NK cell trafficking to the D-LN in the aged mice after IAV infection.

journal_name

Exp Gerontol

journal_title

Experimental gerontology

authors

Duan X,Lu J,Wang H,Liu X,Wang J,Zhou K,Jiang W,Wang Y,Fang M

doi

10.1016/j.exger.2017.06.021

subject

Has Abstract

pub_date

2017-10-01 00:00:00

pages

127-137

eissn

0531-5565

issn

1873-6815

pii

S0531-5565(17)30307-8

journal_volume

96

pub_type

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