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High MAPK p38 activity and low level of IL-10 in intermittent claudication as opposed to stable angina
Örebro universitet, Akademin för naturvetenskap och teknik.ORCID-id: 0000-0001-5069-6120
Örebro universitet, Hälsoakademin.
Örebro universitet, Hälsoakademin.ORCID-id: 0000-0003-1067-8627
Örebro universitet, Hälsoakademin.
Vise andre og tillknytning
2010 (engelsk)Inngår i: International Journal of Angiology, ISSN 0392-9590, E-ISSN 1827-1839, Vol. 29, nr 4, s. 331-337Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

AIM:

The aim of the present pilot study was to relate the activity of MAPK p38 with the levels of pro- and anti-inflammatory cytokines in a small cohort of patients with either stable angina (N=5) or intermittent claudication (N=5) compared to healthy controls (N=10).

METHODS:

The activity of MAPK p38 was determined in peripheral blood mononuclear cells, isolated from whole blood by western blot using phospho-specific anti-MAPK p38 antibodies. Cytokine levels of 11 pro- and anti-inflammatory cytokines were determined from the serum using flow cytometry.

RESULTS:

We found a significant elevation of the MAPK p38 activity in the intermittent claudication group (P=0.0027) compared with the healthy control group whereas the stable angina group showed similar MAPK p38 activity as the healthy control group. The IL-10 level in serum found in the stable angina group was significantly higher compared with both the healthy control group (P=0.0116) and the intermittent claudication group (P=0.0317).

CONCLUSION:

Our results imply that there is a casual relationship between increased levels of the anti-inflammatory cytokines IL-10 and IL-4 and the activity of the MAPK p38. Possibly has IL-10 a protective role that down-regulates the activity of MAPK p38 and thereby further inflammatory processes in stable angina patients.

sted, utgiver, år, opplag, sider
Torino: Minerva Medica , 2010. Vol. 29, nr 4, s. 331-337
Emneord [en]
p38 mitogen-activated protein kinases, Interleukin-10, Intermittent claudication
HSV kategori
Forskningsprogram
Kardiologi
Identifikatorer
URN: urn:nbn:se:oru:diva-12845ISI: 000283516700007PubMedID: 20671651OAI: oai:DiVA.org:oru-12845DiVA, id: diva2:384731
Tilgjengelig fra: 2011-01-10 Laget: 2011-01-03 Sist oppdatert: 2017-12-11bibliografisk kontrollert
Inngår i avhandling
1. Regulatory aspects of innate immune responses
Åpne denne publikasjonen i ny fane eller vindu >>Regulatory aspects of innate immune responses
2011 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Activation of innate immunity is regulated by a variety of signaling molecules within the immune cells. The present thesis was aimed to improve our understanding of innate signaling mechanism and their possible use as bio-indicators of exposure and disease. The first part of the thesis deals with the involvement of TOM1L1 (Target of Myb1 like 1) in innate immune signaling and regulation of inflammatory cytokines in immune cells (study I and II). The initial event of T-cells activation depend on the recruitment of Src family kinases Fyn and Lck, leading to interleukine-2 (IL-2) production in T cells. Understanding the regulatory aspects of IL-2 induction in T-cells is of importance as IL-2 is a key regulator for T-cell proliferation and survival. Interaction screening indicated the ability of TOM1L1 protein to interact with Fyn, and Lck, that is important for IL-2 production in Jurkat T-cells. TOM1L1 silencing decreased the levels of CD3/CD28 dependent induction of IL-2 in Jurkat T-cells, and LPS dependent induction of TNF-α in THP-1. Furthermore, overexpression of TOM1L1 in Jurkat T-cells causes an increase of STAT3 expression. This was accompanied by an increase in the levels of IL-1β dependent induction of IL-6 and TNF-α in THP-1 cells. These results indicate that TOM1L11 participate in regulation of innate immune response. The second part of the thesis deals with development of innate immune signaling responses used as a diagnosis tools for disease and exposure (study III and IV). Inflammatory diseases are associated with innate immune reactions. In response to inflammation, the immune cells release inflammatory cytokines such as IL-1-β, IL-2, IL-6, IL-10, TNF-α and CXCL8. These cytokines are regulated by stress related kinases include MAP kinase proteins such as ERK1-2, JNK, and MAPK p38, through activation of transcription factors AP-1, ATF-2, and NF-AT. In a clinical study, it was observed that activated MAPK p38 has a potential role in the regulation of IL-10 expression in intermittent claudication. However, expression of IL-10 and MAPK p38 was opposed in stable angina group. Therefore, targeting MAPK p38 in inflammatory disease such as cardiovascular diseases, diabetes, and rheumatoid arthritis might be useful in development of treatment strategies. Innate immune reactions can also be used to monitor stress related inflammatory responses following environmental exposure of immune cells. Inflammatory responses of exposure were studied by in vitro exposure to waters from sewage treatment works and recipient waters. The analysis shows that exposure to inland waters can result in activated immune responses and that these responses are both site dependent and vary over time.

sted, utgiver, år, opplag, sider
Örebro: Örebro universitet, 2011. s. 56
Serie
Örebro Studies in Life Science ; 9
Emneord
Innate immunity, TOM1L1, inflammatory responses
HSV kategori
Forskningsprogram
Biologi
Identifikatorer
urn:nbn:se:oru:diva-21384 (URN)978-91-7668-816-8 (ISBN)
Disputas
2011-10-31, Musikhögskolan, hörsal M, Fakultetsgatan 1, Örebro, 10:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2012-01-30 Laget: 2012-01-27 Sist oppdatert: 2017-10-17bibliografisk kontrollert

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