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  • Gao, Hui  (2)
  • Kubo, Hajime  (2)
  • Medizin  (2)
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  • Medizin  (2)
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  • 1
    In: Circulation Research, Ovid Technologies (Wolters Kluwer Health), Vol. 109, No. suppl_1 ( 2011-12-09)
    Kurzfassung: The source of Ca 2+ to hypertrophic signaling after myocardial infarction (MI) is not clearly defined. Transient Receptor Potential Canonical (TRPC) channels could be an important source of hypertrophic Ca 2+ after MI. The objective of this study was to determine if TRPC 4 is a major source of Ca 2+ influx mediating cardiac dysfunction after MI. Methods: Cardiac-specific transgenic mice that express a dominant-negative (dn) TRPC4 that reduces the activity of the TRPC1/4/5 subfamily of channels in the heart were used. MI was produced and in-vivo cardiac function was measured with ECHO. Myocytes were isolated and isoproterenol (ISO) effects on LTCC Current ( I Ca-L ), fractional shortening (FS) and Ca 2+ transients were measured 6 weeks after MI. Results: Baseline ejection fraction (EF) and fractional shortening (FS) were greater in (dn) TRPC4 vs. WT mice. Two weeks after MI, EF and FS were significantly decreased in all animals (WT: 37.1% and 18.2%; (dn) TRPC4: 41.7% and 20.5%), but there was no significant difference between WT and (dn) TRPC4 mice. Six weeks after MI, EF and FS were significant greater in (dn) TRPC4 compared with WT mice (WT: 37.4% and 18.2%; (dn) TRPC4: 52.2% and 27.4%). Heart weight and lung weight were significantly increased after 2 weeks MI, but there were significant lower heart and lung weight in (dn) TRPC4 vs. WT mice after 6 weeks MI. I Ca-L [[Unsupported Character - Codename & shy;]] after 6 weeks MI was smaller than that in sham myocytes, and there was no significant difference between (dn) TRPC4 and WT myocytes. Contractions and Ca 2+ transients were significantly greater in sham and post-MI (dn) TRPC4 vs. WT myocytes. ISO increased contractions and Ca 2+ transients to a similar extent in all myocytes. Conclusions: (dn) TRPC4 mice have greater baseline cardiac and myocyte function. While initial effects of MI were similar to control, there was improved function in these mice by 6 weeks. These results suggest that blocking TRPC4 after MI may reduce pathological cardiac remodeling.
    Materialart: Online-Ressource
    ISSN: 0009-7330 , 1524-4571
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2011
    ZDB Id: 1467838-X
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    Online-Ressource
    Online-Ressource
    Ovid Technologies (Wolters Kluwer Health) ; 2012
    In:  Circulation Research Vol. 111, No. suppl_1 ( 2012-08-03)
    In: Circulation Research, Ovid Technologies (Wolters Kluwer Health), Vol. 111, No. suppl_1 ( 2012-08-03)
    Kurzfassung: T-type Ca²[[Unable to Display Character: + ]] channels (TTCC) are primarily expressed in fetal/neonatal cardiomyocytes and their functional role is not well defined. Here we explored the idea that Ca 2+ influx through TTCC regulates myocyte proliferation. The fact that Mibefradil (TTCC and L-type calcium channel (LTCC) antagonist) inhibits smooth muscles proliferation supports this idea. Our hypothesis is: Blocking TTCC will reduce neonatal cardiomyocyte proliferation. Wild type (WT) and α1G TTCC knockout (α1G-/-) neonatal mice ventricular myocytes (NMVMs) were used. Patch clamp was used to measure TTCC. Flow cytometry was used to determine cell cycle distribution. 1. On day 1 (after birth), TTCC was detected in 35% WT NMVMs (n=31), whereas only 4% α1G-/- NMVMs have TTCC (n=25). On day 7, no TTCC was detected in both WT (n=16) and α1G-/- (n=27). 2. In vivo: On day 1 there’s no significant difference in cell cycle distribution: [88.2%±2.7% in G1/G0, 8.1%±2.8% in G2/M, 3.2%±0.1% in S; n=12] in WT vs. [90.6%±1.6% in G1/G0, 5.7%±1.5% in G2/M, 3.7%±0.3% in S; n=20] in α1G-/-. On day 7 there’s a significant difference: [52.3%±1.6% in G1/G0, 47.7%±1.6% in G2/M; n=28] in WT vs. [68.2%±2.1% in G1/G0, 31.9%±2.1% in G2/M; n=20] in α1G-/-, p 〈 0.05. 3. In vitro: Mono and binucleated myocytes percentage was measured: On day 1 there’s no significant difference. On day 7 there were more binucleated cells in WT: 51%±4% mono and 49%±4% binucleated in WT (n=495) vs. 80%±3% mono and 20%±3% binucleated in α1G-/- (n=1107), p 〈 0.05. Cell surface area (CSA) (um²) in α1G-/- (n=164) was smaller than WT (n=109): 860.3±323.3 in WT vs. 716.7±274.9 in α1G-/- in mono (p 〈 0.005), 1333.9±534.0 in WT vs. 1016.6±315.4 in α1G-/- in binucleated (p 〈 0.001). In 2-month old mice there’s a difference in percentage of mono and binucleated myocytes: [7.3%±3.7% mono, 92.7%±3.6% binucleated; n=687] in WT vs. [30.8%±6.1% mono, 69.2%±6.1% binucleated; n=793] in α1G-/-, p 〈 0.05. CSA in α1G-/- was smaller than in WT: 2267.4±1119.7 in WT vs. 1784.6±683.9 in α1G-/- in mononulceated (p 〈 0.0001), 2419.2±712.4 in WT vs. 2048.3±671.1 in α1G-/- in binucleated (p 〈 0.0001). There is large amount of DNA synthesis in NMVMs after birth, by day 7 most of the WT NMVMs are arrested in G2 and become binucleated. Myocyte without α1G TTCCs did not exit from the cell cycle normally.
    Materialart: Online-Ressource
    ISSN: 0009-7330 , 1524-4571
    RVK:
    Sprache: Englisch
    Verlag: Ovid Technologies (Wolters Kluwer Health)
    Publikationsdatum: 2012
    ZDB Id: 1467838-X
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
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