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Evidence for CD34/SMA positive cells in the left main coronary artery in atherogenesis

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62157124%3A16370%2F16%3A43874488" target="_blank" >RIV/62157124:16370/16:43874488 - isvavai.cz</a>

  • Výsledek na webu

    <a href="http://dx.doi.org/10.1016/j.acthis.2016.04.005" target="_blank" >http://dx.doi.org/10.1016/j.acthis.2016.04.005</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.acthis.2016.04.005" target="_blank" >10.1016/j.acthis.2016.04.005</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Evidence for CD34/SMA positive cells in the left main coronary artery in atherogenesis

  • Popis výsledku v původním jazyce

    Regression of atherosclerosis is a key aspect of preventing further coronary artery disease and understanding which cell type forms smooth muscle cells in atherosclerotic fibrous caps will aid in reducing CAD. Atherogenesis is a complex interplay of cells migrating and proliferating into the vascular wall. CD34 positive hemapoetic stem cells are believed to not transform into vascular smooth muscle cells (SMC). The current study hypothesised that there would be no evidence for CD34(+)/alpha SMC actin(+) cells in atherosclerotic coronary arteries. Aims: To identify CD34(+)/alpha actin positive cells in the fibrous cap and wall of atherosclerotic plaques in the coronary artery. Methods: Male New Zealand White rabbits were fed a diet containing 0.5% cholesterol and 1% methionine for 4 weeks, then 9 weeks of normal diet to induce regression. Immunohistochemistry was used to detect CD34(+) haematopoietic progenitor cells and SMC actin. Results: In the fibrous cap, the majority of cells were CD34(-)/alpha SMC actin(+) spindle shaped cells. However very rare populations of CD34(+)/alpha SMC actin(+) and CD34(+)/alpha SMC actin(-) cells were also present but these cells were not spindle shaped. Conclusion: Our study found that CD34(+)/alpha SMC actin spindle shaped cells were absent from the fibrous cap. Moreover, the predominant cell population were the vascular smooth muscle cells (CD34(-)/alpha SMC actin(+)) but (CD34(+)/alpha SMC actin(+)) cells were also present. This model could be used to understand the role of each SMC population subtype to hasten atherosclerotic regression in the coronary artery.

  • Název v anglickém jazyce

    Evidence for CD34/SMA positive cells in the left main coronary artery in atherogenesis

  • Popis výsledku anglicky

    Regression of atherosclerosis is a key aspect of preventing further coronary artery disease and understanding which cell type forms smooth muscle cells in atherosclerotic fibrous caps will aid in reducing CAD. Atherogenesis is a complex interplay of cells migrating and proliferating into the vascular wall. CD34 positive hemapoetic stem cells are believed to not transform into vascular smooth muscle cells (SMC). The current study hypothesised that there would be no evidence for CD34(+)/alpha SMC actin(+) cells in atherosclerotic coronary arteries. Aims: To identify CD34(+)/alpha actin positive cells in the fibrous cap and wall of atherosclerotic plaques in the coronary artery. Methods: Male New Zealand White rabbits were fed a diet containing 0.5% cholesterol and 1% methionine for 4 weeks, then 9 weeks of normal diet to induce regression. Immunohistochemistry was used to detect CD34(+) haematopoietic progenitor cells and SMC actin. Results: In the fibrous cap, the majority of cells were CD34(-)/alpha SMC actin(+) spindle shaped cells. However very rare populations of CD34(+)/alpha SMC actin(+) and CD34(+)/alpha SMC actin(-) cells were also present but these cells were not spindle shaped. Conclusion: Our study found that CD34(+)/alpha SMC actin spindle shaped cells were absent from the fibrous cap. Moreover, the predominant cell population were the vascular smooth muscle cells (CD34(-)/alpha SMC actin(+)) but (CD34(+)/alpha SMC actin(+)) cells were also present. This model could be used to understand the role of each SMC population subtype to hasten atherosclerotic regression in the coronary artery.

Klasifikace

  • Druh

    J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

  • CEP obor

    CE - Biochemie

  • OECD FORD obor

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2016

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    ACTA HISTOCHEMICA

  • ISSN

    0065-1281

  • e-ISSN

  • Svazek periodika

    118

  • Číslo periodika v rámci svazku

    4

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    5

  • Strana od-do

    413-417

  • Kód UT WoS článku

    000378958100012

  • EID výsledku v databázi Scopus