Metabolic dysfunction and inflammatory disease: the role of stromal fibroblasts.
Metabolic dysfunction and inflammatory disease: the role of stromal fibroblasts.
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DOI:
10.1111/febs.15644
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发表时间:
2021-10
期刊:
影响因子:
--
通讯作者:
Jones SW
中科院分区:
文献类型:
--
作者:
Farah H;Young SP;Mauro C;Jones SW
Stromal fibroblasts are central mediators of chronic inflammatory disease. Changes to fibroblast metabolism (including glycolysis, oxidative phosphorylation, pentose phosphate pathway, glutamine metabolism and lactate transport) fuels and underpins the switch in fibroblast phenotype towards an inflammatory‐activated phenotype that drives chronic inflammation. Cancer‐associated fibroblasts drive tumour progression, activated synoviocytes drive joint inflammation, and activated myoblasts drive fibrotic disorders including chronic kidney disease, pulmonary fibrosis, heart disease and liver disease. Mesenchymal stromal fibroblasts have emerged as key mediators of the inflammatory response and drivers of localised inflammation, in part through their interactions with resident and circulating immune cells at inflammatory sites. As such, they have been implicated in a number of chronic inflammatory conditions as well as in tumour progression through modifying the microenvironment. The connection between metabolic changes and altered phenotype of fibroblasts in inflammatory microenvironments has clear implications for our understanding of how chronic inflammation is regulated and for the development of new anti‐inflammatory therapeutics. In this review, we consider the evidence that changes to fibroblast metabolic state underpin chronic inflammation. We examine recent research on fibroblast metabolism in inflammatory microenvironments and consider their involvement in inflammation, providing insight into the role of fibroblasts and metabolism in mediating inflammatory disease progression namely cancer, arthritis and fibrotic disorders including chronic kidney disease, pulmonary fibrosis, heart disease and liver disease.
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影响因子:
11.2
作者:
Bavik, C;Coleman, I;Nelson, PS
通讯作者:
Nelson, PS
DOI:
10.1083/jcb.201704053
发表时间:
2017-11-06
期刊:
The Journal of cell biology
影响因子:
--
作者:
Erdogan B;Ao M;White LM;Means AL;Brewer BM;Yang L;Washington MK;Shi C;Franco OE;Weaver AM;Hayward SW;Li D;Webb DJ
通讯作者:
Webb DJ
影响因子:
2.1
作者:
Cao W;Shi P;Ge JJ
通讯作者:
Ge JJ
影响因子:
--
作者:
Fu Y;Liu S;Yin S;Niu W;Xiong W;Tan M;Li G;Zhou M
通讯作者:
Zhou M
DOI:
10.1146/annurev-pathol-121808-102144
发表时间:
2010
期刊:
Annual review of pathology
影响因子:
--
作者:
Coppé JP;Desprez PY;Krtolica A;Campisi J
通讯作者:
Campisi J