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Notes:

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Volume 8, Issue 3 (Suppl)

J Clin Cell Immunol, an open access journal

ISSN: 2155-9899

Euro Immunology 2017

June 29-July 01, 2017

June 29-July 01, 2017 Madrid, Spain

8

th

European

Immunology Conference

Distinct upstream role of type I IFN signaling in hematopoietic stem cell-derived and epithelial resident

cells for concerted recruitment of Ly-6C

hi

monocytes and NK cells via CCL2-CCL3 cascade

Seong Kug Eo, Jin Hyoung Kim, Ajit Mahadev Patil, Jin Young Choi, Seong Bum Kim

and

Erdenebileg Uyangaa

Chonbuk National University, South Korea

T

ype I interferon (IFN-I)-dependent orchestrated mobilization of innate cells in inflamed tissues is believed to play a critical role in

controlling replication and CNS-invasion of herpes simplex virus (HSV). However, the crucial regulators and cell populations that

are affected by IFN-I to establish the early environment of innate cells in HSV-infected mucosal tissues are largely unknown. Here, we

found that IFN-I signaling promoted the differentiation of CCL2-producing Ly-6C

hi

monocytes and IFN-

γ

/granzyme B-producing

NK cells, whereas deficiency of IFN-I signaling induced Ly-6C

lo

monocytes producing CXCL1 and CXCL2. More interestingly,

recruitment of Ly-6C

hi

monocytes preceded that of NK cells with the levels peaked at 24 h post-infection in IFN-I–dependent manner,

which was kinetically associated with the CCL2-CCL3 cascade response. Early Ly-6C

hi

monocyte recruitment was governed by CCL2

produced from hematopoietic stem cell (HSC)-derived leukocytes, whereas NK cell recruitment predominantly depended on CC

chemokines produced by resident epithelial cells. Also, IFN-I signaling in HSC-derived leukocytes appeared to suppress Ly-6G

hi

neutrophil recruitment to ameliorate immunopathology. Finally, tissue resident CD11b

hi

F4/80

hi

macrophages and CD11c

hi

EpCAM

+

dendritic cells appeared to produce initial CCL2 for migration-based self-amplification of early infiltrated Ly-6C

hi

monocytes upon

stimulation by IFN-I produced from infected epithelial cells. Ultimately, these results decipher a detailed IFN-I-dependent pathway

that establishes orchestrated mobilization of Ly-6C

hi

monocytes and NK cells through CCL2-CCL3 cascade response of HSC-derived

leukocytes and epithelium-resident cells. Therefore, this cascade response of resident-to-hematopoietic-to-resident cells that drives

cytokine-to-chemokine-to-cytokine production to recruit orchestrated innate cells is critical for attenuation of HSV replication in

inflamed tissues.

Biography

Seong Kug EO’s lab has focused on unveiling how hosts response to pathogen infection. They have used various infectious models to prove host responses upon

pathogenic infection. In recent, EO’s lab has found the detailed pathway that IFN-I signal pathway orchestrated environments to provide effective protection against

mucosal viral infection (PLoS Pathog., 2016). Moreover, EO’s lab is expert on viral acute encephalitis caused by flaviviral infection. They have got many reports to

unveil how immune system works on viral encephalitis caused by Japanese encephalitis virus (J. Neuroinflammation, 2014 and 2016).

vetvirus@chonbuk.ac.kr

Seong Kug EO et al., J Clin Cell Immunol 2017, 8:3(Suppl)

DOI: 10.4172/2155-9899-C1-037