2020
DOI: 10.1073/pnas.1922729117
|View full text |Cite
|
Sign up to set email alerts
|

Engineering a potent receptor superagonist or antagonist from a novel IL-6 family cytokine ligand

Abstract: Interleukin-6 (IL-6) family cytokines signal through multimeric receptor complexes, providing unique opportunities to create novel ligand-based therapeutics. The cardiotrophin-like cytokine factor 1 (CLCF1) ligand has been shown to play a role in cancer, osteoporosis, and atherosclerosis. Once bound to ciliary neurotrophic factor receptor (CNTFR), CLCF1 mediates interactions to coreceptors glycoprotein 130 (gp130) and leukemia inhibitory factor receptor (LIFR). By increasing CNTFR-mediated binding to these cor… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
13
0

Year Published

2021
2021
2023
2023

Publication Types

Select...
7
1
1

Relationship

1
8

Authors

Journals

citations
Cited by 18 publications
(15 citation statements)
references
References 59 publications
2
13
0
Order By: Relevance
“…Like F152 and K155 of CNTF, the two conserved CLCF1 residues F178 and K181 also serve as key anchor points engaging LIFR residues (S310, N313, V315, I322, G324, and V326) (Fig. 2H), consistent with previous mutagenesis studies ( 18 , 20 ). CLCF1 helix B does not make significant contacts with the N-terminal loop of LIFR D4 as CNTF helix B does, because CLCF1 helix B is slightly shorter than CNTF helix B at the C-terminus.…”
Section: Resultssupporting
confidence: 89%
“…Like F152 and K155 of CNTF, the two conserved CLCF1 residues F178 and K181 also serve as key anchor points engaging LIFR residues (S310, N313, V315, I322, G324, and V326) (Fig. 2H), consistent with previous mutagenesis studies ( 18 , 20 ). CLCF1 helix B does not make significant contacts with the N-terminal loop of LIFR D4 as CNTF helix B does, because CLCF1 helix B is slightly shorter than CNTF helix B at the C-terminus.…”
Section: Resultssupporting
confidence: 89%
“…This might greatly impact the selectiveness of a given inhibitor's effect on downstream signalling, so that finer blockade of the effects of a specific cytokine might be achieved [305]. Also in line with this, a recent study showed that targeted mutagenesis of different residues in CLC, which mediate interactions in the CNTF-CNTFR-LIFR-gp130/IL6ST signalling complex, can yield novel recombinant variants with distinct functions [306].…”
Section: Therapeutic Targeting Of Gp130/il6st Signallingmentioning
confidence: 92%
“…Kim, Jun W et al have engineered CLCF1 variants that can inhibit or activate CNTFR. The application of it in atherosclerosis might be meaningful research ( 80 ).…”
Section: Interleukin-6 Family Members and Cardiovascular Diseasementioning
confidence: 99%