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. 2020 Dec 11;11:552613. doi: 10.3389/fimmu.2020.552613

Table 1.

Functional studies of signaling molecules in carbon nanotube (CNT)-induced pulmonary immune responses using knockout (KO) mice.

KO mice CNTs Effects Findings in KO mice References
IL-1R KO long, rod-like MWCNTs
(XNRI MWNT-7)
OD: >50 nm L: ~13 µm long, tangled MWCNTs OD: 8–15 nm L: 10–50 µm
acute inflammation Long, rod-like MWCNTs, but not long, tangled MWCNTs, increase neutrophils in BAL and pro-inflammatory cytokine and chemokine expression in lung tissues 16 h post-exposure in WT mice, which are attenuated in IL-1R KO mice.
Long, rod-like MWCNTs induce Th2-type inflammation on day 28 post-exposure in WT mice, which is not affected in IL-1R KO mice.
(29)
IL-1R KO MWCNTs (XNRI MWNT-7)
D: 49±13.4 nm L: 3.86±1.94 µm
acute inflammation MWCNT-induced acute inflammation is suppressed in IL-1R KO mice 24 h post-exposure, compared with WT mice, whereas IL-1R KO does not suppress inflammation on day 28 post-exposure, determined by the numbers of total cells, mononuclear cells, and neutrophils and the levels of IL-6, IL-12p40, and CXCL1 in BAL. (30)
caspase-1 KO MWCNTs (FA-21)
D: 27 nm L: 5–15 µm
acute inflammation The level of IL-1β, the number of total cells, and the number of neutrophils in BAL are significantly increased by MWCNTs on day 1 post-exposure in WT mice, but not in caspase-1 KO mice.
The number of eosinophils in BAL is significantly increased by MWCNTs on day 1 post-exposure in WT mice, which is not affected in caspase-1 KO mice.
(31)
ST2 KO MWCNTs
D: 22.5±1.3 nm L: 10–100 µm
chronic inflammation
type 2 immune response
The induction of inflammation, fibrosis, and functional damage by MWCNTs in the lung on day 30 post-exposure is inhibited in mast cell-deficient KitW-sh mice and ST2 KO mice, compared with WT mice. Reconstitution of KitW-sh mice with WT BMMCs restores these MWCNT-induced pathological outcomes, whereas that with ST2 KO BMMCs does not. (32)
IL-13 KO MWCNTs (FA-21)
D: 27 nm L: 5–15 µm
type 2 immune response MWCNTs increase eosinophils in WLL 24 h post-exposure in WT mice, but not in IL-13 KO mice. (33)
IL-33 KO MWCNTs (FA-21)
D: 27 nm L: 5–15 µm
type 2 immune response MWCNTs increase eosinophils in WLL 24 h post-exposure in WT mice, but not in IL-33 KO mice. (33)
IL-33 KO MWCNTs
D: 22.5±1.3 nm L: 10–100 µm
chronic inflammation
type 2 immune response
The number of eosinophils in BAL is increased by MWCNTs on day 30 post-exposure in WT mice, which is attenuated in IL-33 KO mice.
MWCNTs induce fibrosis near the airways in WT mice, but not in IL-33 KO mice, on day 30 post-exposure.
(34)
STAT6 KO MWCNTs (XNRI MWNT-7)
D: 49±13.4 nm L: 3.86±1.94 µm
type 2 immune response The level of IL-5 is elevated by MWCNTs in the BAL from WT mice, but not in the BAL from STAT6 KO mice, 24 h post-exposure.
MWCNT-induced fibrotic phenotype is weakened in STAT6 KO lung tissues, compared with WT lung tissues, on day 28 post-exposure.
(30)

D, diameter; L, length; OD, outside diameter; WLL, whole lung lavage.