Promotion of experimental autoimmune encephalomyelitis upon neutrophil granulocytes' stimulation with formyl-methionyl-leucyl-phenylalanine (fMLP) peptide. (September 2015)
- Record Type:
- Journal Article
- Title:
- Promotion of experimental autoimmune encephalomyelitis upon neutrophil granulocytes' stimulation with formyl-methionyl-leucyl-phenylalanine (fMLP) peptide. (September 2015)
- Main Title:
- Promotion of experimental autoimmune encephalomyelitis upon neutrophil granulocytes' stimulation with formyl-methionyl-leucyl-phenylalanine (fMLP) peptide
- Authors:
- Kilic, Ahmet Kasim
Esendagli, Gunes
Sayat, Guliz
Talim, Beril
Karabudak, Rana
Kurne, Asli Tuncer - Abstract:
- <abstract> <title>Abstract</title> <p>It has been acknowledged that neutrophil granulocytes, the common mediators of immune responses against extracellular bacteria, can also intercede autoimmune reactions such as experimental autoimmune encephalomyelitis (EAE). Formyl-methionyl-leucyl-phenylalanine (fMLP) is a microbial peptide that can be well-tolerated when intravenously administered and can directly lead to activation and accumulation of neutrophils into the blood circulation. Here, this antigenic peptide was injected to the mice at the induction of EAE, and the immunological and pathological outcomes were assessed. As a peripheral immune organ, spleen of the animals that received fMLP contained considerably high percentages of Gr-1<sup>hi</sup>Ly7/4<sup>hi</sup> mature neutrophils. In the sera samples, only a slight difference was determined in Th1/Th2/Th17-related cytokine levels. Expression of CXCR1 or CXCR2 chemokine receptors was not significantly modulated in EAE with or without fMLP which might indicate a direct role for this antigenic peptide on neutrophil accumulation. Even though fMLP administration did not propone the clinical (symptomatic) onset of the disease, the animals showed severe body conditions with higher EAE scores. Accordingly, the expression of TNF-α and CXCL1 inflammatory mediators in the brain was increased in fMLP–EAE group. In conclusion, with its potent capacity to mobilize neutrophils and to stimulate innate immune cells, fMLP peptide can be<abstract> <title>Abstract</title> <p>It has been acknowledged that neutrophil granulocytes, the common mediators of immune responses against extracellular bacteria, can also intercede autoimmune reactions such as experimental autoimmune encephalomyelitis (EAE). Formyl-methionyl-leucyl-phenylalanine (fMLP) is a microbial peptide that can be well-tolerated when intravenously administered and can directly lead to activation and accumulation of neutrophils into the blood circulation. Here, this antigenic peptide was injected to the mice at the induction of EAE, and the immunological and pathological outcomes were assessed. As a peripheral immune organ, spleen of the animals that received fMLP contained considerably high percentages of Gr-1<sup>hi</sup>Ly7/4<sup>hi</sup> mature neutrophils. In the sera samples, only a slight difference was determined in Th1/Th2/Th17-related cytokine levels. Expression of CXCR1 or CXCR2 chemokine receptors was not significantly modulated in EAE with or without fMLP which might indicate a direct role for this antigenic peptide on neutrophil accumulation. Even though fMLP administration did not propone the clinical (symptomatic) onset of the disease, the animals showed severe body conditions with higher EAE scores. Accordingly, the expression of TNF-α and CXCL1 inflammatory mediators in the brain was increased in fMLP–EAE group. In conclusion, with its potent capacity to mobilize neutrophils and to stimulate innate immune cells, fMLP peptide can be used to aggravate immune reactions in EAE. This observation may indicate that the strength of innate immune responses particularly at the induction phase of EAE might influence the clinical course of the disease.</p> </abstract> … (more)
- Is Part Of:
- Autoimmunity. Volume 48:Number 6(2015)
- Journal:
- Autoimmunity
- Issue:
- Volume 48:Number 6(2015)
- Issue Display:
- Volume 48, Issue 6 (2015)
- Year:
- 2015
- Volume:
- 48
- Issue:
- 6
- Issue Sort Value:
- 2015-0048-0006-0000
- Page Start:
- 423
- Page End:
- 428
- Publication Date:
- 2015-09
- Subjects:
- Autoimmunity -- Periodicals
Autoimmune diseases -- Periodicals
571.973 - Journal URLs:
- http://informahealthcare.com/journal/aut ↗
http://informahealthcare.com ↗
http://www.gbhap.com/journals/350/350-top.htm ↗ - DOI:
- ↗
- Languages:
- English
- ISSNs:
- 0891-6934
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1828.345000
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British Library STI - ELD Digital store - Ingest File:
- 3171.xml