کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2190687 1097809 2012 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Phospholemman is a negative feed-forward regulator of Ca2+ in β-adrenergic signaling, accelerating β-adrenergic inotropy
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Phospholemman is a negative feed-forward regulator of Ca2+ in β-adrenergic signaling, accelerating β-adrenergic inotropy
چکیده انگلیسی

Sympathetic stimulation enhances cardiac contractility by stimulating β-adrenergic signaling and protein kinase A (PKA). Recently, phospholemman (PLM) has emerged as an important PKA substrate capable of regulating cytosolic Ca2+ transients. However, it remains unclear how PLM contributes to β-adrenergic inotropy. Here we developed a computational model to clarify PLM's role in the β-adrenergic signaling response. Simulating Na+ and sarcoplasmic reticulum (SR) Ca2+ clamps, we identify an effect of PLM phosphorylation on SR unloading as the key mechanism by which PLM confers cytosolic Ca2+ adaptation to long-term β-adrenergic receptor (β-AR) stimulation. Moreover, we show that phospholamban (PLB) opposes and overtakes these actions on SR load, forming a negative feed-forward loop in the β-adrenergic signaling cascade. This network motif dominates the negative feedback conferred by β-AR desensitization and accelerates β-AR-induced inotropy. Model analysis therefore unmasks key actions of PLM phosphorylation during β-adrenergic signaling, indicating that PLM is a critical component of the fight-or-flight response.

1.SR Ca2+ load specifies the size of Ca2+ transients during CICR.2.PLB increases SR load by biasing diastolic Ca2+ extrusion toward SERCA.3.PLM decreases SR load by driving Na+ extrusion and biasing diastolic Ca2+ extrusion toward NCX.4.Ca2+ adaptation occurs because Na+/K+ dynamics lag behind SERCA dynamics.5.Receptor desensitization weakly contributes to Ca2+ adaptation, highlighting a negative feed-forward loop formed by PLB and PLM. This negative feed-forward network motif accelerates β-adrenergic inotropy.Figure optionsDownload high-quality image (178 K)Download as PowerPoint slideHighlights
► PLM confers cytosolic Ca2+ adaptation via manipulation of SR load.
► PLM and PLB form a negative feed-forward loop in β-adrenergic signaling.
► PLM phosphorylation accelerates β-adrenergic stimulation enhanced contractility.
► PLM is therefore a fundamentally important part of the fight-or-flight response.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular and Cellular Cardiology - Volume 52, Issue 5, May 2012, Pages 1048–1055
نویسندگان
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