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Dendritic cells in subcutaneous and epicardial adipose tissue of subjects with type 2 diabetes, obesity, and coronary artery disease

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F19%3A00078037" target="_blank" >RIV/00023001:_____/19:00078037 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/19:10394874 RIV/00064165:_____/19:10394874

  • Result on the web

    <a href="https://www.hindawi.com/journals/mi/2019/5481725/" target="_blank" >https://www.hindawi.com/journals/mi/2019/5481725/</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1155/2019/5481725" target="_blank" >10.1155/2019/5481725</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Dendritic cells in subcutaneous and epicardial adipose tissue of subjects with type 2 diabetes, obesity, and coronary artery disease

  • Original language description

    Dendritic cells (DCs) are professional antigen-presenting cells contributing to regulation of lymphocyte immune response. DCs are divided into two subtypes: CD11c-positive conventional or myeloid (cDCs) and CD123-positive plasmacytoid (pDCs) DCs. The aim of the study was to assess DCs (HLA-DR+ lineage-) and their subtypes by flow cytometry in peripheral blood and subcutaneous (SAT) and epicardial (EAT) adipose tissue in subjects with (T2DM, n=12) and without (non-T2DM, n=17) type 2 diabetes mellitus undergoing elective cardiac surgery. Subjects with T2DM had higher fasting glycemia (8.6 +/- 0.7 vs. 5.8 +/- 0.2mmol/l, p&lt;0.001) and glycated hemoglobin (52.0 +/- 3.4 vs. 36.9 +/- 1.0mmol/mol, p&lt;0.001) and tended to have more pronounced inflammation (hsCRP: 9.8 +/- 3.1 vs. 5.1 +/- 1.9mg/ml, p=0.177) compared with subjects without T2DM. T2DM was associated with reduced total DCs in SAT (1.57 +/- 0.65 vs. 4.45 +/- 1.56% for T2DM vs. non-T2DM, p=0.041) with a similar, albeit insignificant, trend in EAT (0.996 +/- 0.33 vs. 2.46 +/- 0.78% for T2DM vs. non-T2DM, p=0.171). When analyzing DC subsets, no difference in cDCs was seen between any of the studied groups or adipose tissue pools. In contrast, pDCs were increased in both SAT (13.5 +/- 2.0 vs. 4.6 +/- 1.9% of DC cells, p=0.005) and EAT (29.1 +/- 8.7 vs. 8.4 +/- 2.4% of DC, p=0.045) of T2DM relative to non-T2DM subjects as well as in EAT of the T2DM group compared with corresponding SAT (29.1 +/- 8.7 vs. 13.5 +/- 2.0% of DC, p=0.020). Neither obesity nor coronary artery disease (CAD) significantly influenced the number of total, cDC, or pDC in SAT or EAT according to multiple regression analysis. In summary, T2DM decreased the amount of total dendritic cells in subcutaneous adipose tissue and increased plasmacytoid dendritic cells in subcutaneous and even more in epicardial adipose tissue. These findings suggest a potential role of pDCs in the development of T2DM-associated adipose tissue low-grade inflammation.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30202 - Endocrinology and metabolism (including diabetes, hormones)

Result continuities

  • Project

    <a href="/en/project/NV15-26854A" target="_blank" >NV15-26854A: The role of epicardial adipose tissue in heart disease: novel mechanisms of action and its therapeutic modulation</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Mediators of inflammation [online]

  • ISSN

    0962-9351

  • e-ISSN

  • Volume of the periodical

    2019

  • Issue of the periodical within the volume

    May 9

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    7

  • Pages from-to

    "art. no. 5481725"

  • UT code for WoS article

    000468514100001

  • EID of the result in the Scopus database

    2-s2.0-85068368035