2021
DOI: 10.1016/j.cyto.2021.155458
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A primer on cytokines

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Cited by 49 publications
(49 citation statements)
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“…In human fibrosarcoma-derived cell line, INF-gamma induces expression of Smad7 mediated by phosphorylation and activation of the transcription factor STAT1 through JAK1 thereby preventing the interaction of Smad3 with TGF-β receptor ( Majoros et al, 2017 ). Signal-transduction pathways induced by JAK/STAT and TGF-β signaling may be affected by transmodulating interactions between Smads and STATs ( Chauhan et al, 2021 ). In conclusion, apart from regulating T-lymphocyte activation, TGF-β cross connects with JAK/STAT signaling to regulate plethora of pathophysiological process via Smads which includes activation of hematopoiesis, TGF-β fibrogenic responses in hepatic stellate cells, transcription of genes regulating EMT and regulating pluropotency and differentiations of cells ( Figure 7 ).…”
Section: Introductionmentioning
confidence: 99%
“…In human fibrosarcoma-derived cell line, INF-gamma induces expression of Smad7 mediated by phosphorylation and activation of the transcription factor STAT1 through JAK1 thereby preventing the interaction of Smad3 with TGF-β receptor ( Majoros et al, 2017 ). Signal-transduction pathways induced by JAK/STAT and TGF-β signaling may be affected by transmodulating interactions between Smads and STATs ( Chauhan et al, 2021 ). In conclusion, apart from regulating T-lymphocyte activation, TGF-β cross connects with JAK/STAT signaling to regulate plethora of pathophysiological process via Smads which includes activation of hematopoiesis, TGF-β fibrogenic responses in hepatic stellate cells, transcription of genes regulating EMT and regulating pluropotency and differentiations of cells ( Figure 7 ).…”
Section: Introductionmentioning
confidence: 99%
“…This feature is driven through helpful and effective mutations within these genes, which may lead to a coevolutionary adaptation in host-pathogen interactions. In this regard, the results of a survey showed that out of 25 genes with highest evolutionary divergence in humans, seven genes belong to cytokines (e.g., ILs) [ 43 , 66 ]. Interestingly, despite the occurrence of evolutionary divergence among cytokine genes (such as IL genes), some structural resemblance can still be seen.…”
Section: Genomics Of Ilsmentioning
confidence: 99%
“…The sharing of cytokine receptor chains and signalling pathways provides a mechanism for functional redundancy. The existence of more than one receptor for that cytokine can explain the pleiotropic effects of a single cytokine [8], while the expression and distribution of cytokine receptors among the different cell types determine the specificity of cytokine activity [9]. The combinatorial array of cell type-specific and context-specific expression of cytokines and receptor complexes is responsible for various host protective immunity, organ development and metabolism, haematopoiesis, tumorigenesis, development, and inflammation [10].…”
Section: Type I Cytokine Receptorsmentioning
confidence: 99%