Nejvíce citovaný článek - PubMed ID 3047139
Fibroblasts actively participate in cellular immune responses in connective tissues, when activated by signals abundant at inflammatory sites, i.e. cytokines and bacterial products. This is manifested by the generation of proinflammatory cytokines and by presenting antigens to proliferating T cells. The array of cytokines generated by immune-activated fibroblasts is determined by the stimulant and is controlled at multiple regulatory levels, such as transcription, translation, posttranslational modifications, the signal transduction pathways which are activated, the timing of expression as well as compartmentation within the producing cell. In general, cytokines with potential of tissue damage, i.e. IL-1 alpha and, to a lesser extent, IL-6, are more tightly regulated than cytokines with restricted target cell specificity (i.e. CSFs). Deviations in the pattern of expression of IL-1 alpha in pathological conditions affecting connective tissues are described; a long-lasting suppression of IL-1 alpha production was observed in dermal fibroblasts of mice suffering from chronic graft-vs.-host disease (cGVHD), while some oncogene-transformed fibroblastoid cell lines were shown to generate this cytokine in a constitutive manner and as a result expressed reduced tumorigenicity. The latter is due to the adjuvant effects of IL-1 alpha, expressed by the malignant cells, which induce potent antitumor specific immune responses which ultimately lead to its eradication. Understanding the molecular mechanisms which control cytokine production in fibroblasts may enrich our knowledge of connective tissue homeostasis and deviations from it in pathological states. The latter may also lead to the development of novel therapeutical means for controlling chronic inflammatory diseases or malignancies.
- MeSH
- aktivace lymfocytů MeSH
- buňky 3T3 MeSH
- cytokiny biosyntéza farmakologie MeSH
- embryo savčí cytologie MeSH
- faktory stimulující kolonie biosyntéza MeSH
- fibroblasty účinky léků imunologie metabolismus MeSH
- homeostáza MeSH
- interleukin-1 biosyntéza MeSH
- interleukin-6 biosyntéza MeSH
- kultivované buňky MeSH
- messenger RNA biosyntéza MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- nemoc štěpu proti hostiteli imunologie patologie MeSH
- pojivová tkáň imunologie patologie fyziologie MeSH
- prezentace antigenu MeSH
- radiační chiméra MeSH
- rekombinantní proteiny farmakologie MeSH
- T-lymfocyty imunologie MeSH
- transformované buněčné linie MeSH
- transfuze leukocytů MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cytokiny MeSH
- faktory stimulující kolonie MeSH
- interleukin-1 MeSH
- interleukin-6 MeSH
- messenger RNA MeSH
- rekombinantní proteiny MeSH