Published online before print June 7, 2007, doi: 10.1161/CIRCRESAHA.107.155721
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
© 2007 American Heart Association, Inc.
Cellular Biology |
Gene Therapy to Inhibit the Calcium Channel ß Subunit
Physiological Consequences and Pathophysiological Effects in Models of Cardiac Hypertrophy
From the Division of Cardiology (E.C., G.A.R.C., E.K., M.M., H.C.C., E.M.), Johns Hopkins University School of Medicine, Baltimore, Md.
Correspondence to Eduardo Marbán, MD, PhD, 858 Ross Building, 720 Rutland Avenue. Baltimore, MD 21205. E-mail marban{at}jhmi.edu
 |
Abstract |
|---|
 Top Abstract IntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
Calcium cycling figures prominently in excitation-contraction coupling and in various signaling cascades involved in the development of left ventricular hypertrophy. We hypothesized that genetic suppression of the L-type calcium channel accessory ß-subunit would modulate calcium current and suppress cardiac hypertrophy. A short hairpin RNA template sequence capable of mediating the knockdown of the L-type calcium channel accessory ß-subunit gene was incorporated into a lentiviral vector (PPT.CG.H1.ß2). Transduction of ventricular myocytes in vivo with the active short hairpin RNA partially inhibited the L-type calcium current. In neonatal rat cardiomyocytes, L-type calcium channel accessory ß-subunit gene knockdown reduced calcium transient amplitude. Similarly, [3H]leucine incorporation was attenuated in PPT.CG.H1.ß2-transduced neonatal rat cardiomyocytes compared with nonsilencing controls in a phenylephrine-induced hypertrophy model. In vivo gene transfer attenuated the hypertrophic response in an aortic-banded rat model of left ventricular hypertrophy, with reduced left ventricular wall thickness and heart weight/body weight ratios in PPT.CG.H1.ß2-injected rats at four weeks post transduction. Fractional shortening was preserved in rats treated with PPT.CG.H1.ß2. These findings indicate that knockdown of L-type calcium channel accessory ß-subunit is capable of attenuating the hypertrophic response both in vitro and in vivo without compromising systolic performance. Suppression of the calcium channel ß subunit may represent a novel and useful therapeutic strategy for left ventricular hypertrophy.
Key Words: hypertrophy • calcium • gene therapy
|
Introduction |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
Calcium cycling in the heart is triggered by calcium influx through L-type calcium channels.1 Such calcium channels are present and functionally important not only in cardiac myocytes but also in diverse smooth muscles and in neurons. Enhancement of calcium-regulated signaling pathways contributes to the development of left ventricular hypertrophy (LVH).2 Thus, calcium channel inhibition represents a logical approach to treatment of LVH. Gene therapy allows for more directed and organ-specific delivery and thus may avoid undesired systemic effects, which may account in part for the limited clinical benefit observed with these agents.3
L-type calcium channels are heteromultimers of various subunits. The accessory ß subunit (LTCCß) not only favors the trafficking of the calcium channel to the surface membrane, but also enhances the probability of channel opening4–7 resulting in increased calcium current. Interestingly, upregulation of a splice variant of the LTCCß (ß2a) has been previously described in failing human cardiomyocytes.8 Whether or not ß subunits are upregulated in hypertrophy, we hypothesized that suppression of LTCCß might represent an attractive means to inhibit calcium influx, attenuate calcium-dependent signaling and ultimately prevent or treat LVH.
Using RNA interference technology to selectively modulate the expression of the gene of interest, we studied the physiological effects of LTCCß modulation in native cardiac cells, and the effects in a cellular model of hypertrophy. To further investigate the effects of LTCCß downregulation in cardiac hypertrophy, we performed in vivo gene transfer of an "advanced" generation lentiviral vector capable of permanently modulating the expression of LTCCß. A rat pressure-overload LVH model was implemented to test the potential beneficial effect of modulating the expression of the L-type calcium channel accessory ß subunit.
|
Materials and Methods |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
For a detailed Materials and Methods, please see the online data supplement available at http://circres.ahajournals.org.
Short Hairpin RNA Design and Vector Production
A series of short interference RNA duplexes (siRNAs) against the D2 conserved domain9 of LTCCß were designed according to published algorithms10 and synthesized. The three most active sequences and one scrambled, nonsilencing (NS) sequence were designed into a short hairpin RNA (shRNA) oligonucleotide. These three active shRNAs and one NS-shRNA sequence were screened using heterologous transfection and flow cytometry analysis (FACS) as described in the next section. The entire shRNA expression cassette was incorporated into a lentiviral vector plasmid (provided by Dr Inder Verma, Salk Institute, San Diego, Calif) (Figure 1A). For the heterologous cotransfection experiments (see below) CMV-green fluorescent protein (GFP) was removed resulting in shRNA vectors PPT.H1.ß2 and PPT.H1.NS. For viral vector production from these plasmids, the four-plasmid transient transfection of 293 cells was performed as previously described.11–13 For in vivo gene transfer efficiency experiments, the cDNA for nuclear-localized ß-galactosidase (LacZnls) was subcloned in place of the GFP gene and vector produced as described.
|
90%.
Cotransfection Heterologous Expression
To establish the knockdown efficacy of the PPT.CG.H1.ß2 sequences, HEK293 cells were cotransfected with pLTCCß–GFP and equimolar ratios of the vector plasmids PPT.H1.ß2 or PPT.H1.NS. Twenty-four hours after transfection, ß2-GFP expression was established by fluorescence microscopy and quantified by flow cytometric analysis.The most active shRNA against the LTCCß (target DNA sequence: 5'- AAC ATG AGG CTA CAG CAT GAA -3') was used for both in vitro and in vivo experiments.
Primary Culture of Neonatal Rat Cardiac Ventricular Myocytes
Neonatal rat cardiac myocytes (NRCMs) were isolated from 1 to 2 day-old rats and cultured as previously described.14,15 The cells were maintained at 37°C in the presence of 5% CO2 in a humidified incubator.
Single Cell Electrophysiology
Myocytes were isolated from the left ventricle of adult rats, in a Langerdorff perfusion system as previously described.16 A xenon arc lamp was used to view GFP fluorescence and therefore recognize transduced cells. Membrane currents were recorded using the whole-cell patch clamp technique.
Calcium Transients
NRCMs were plated into 35 mm glass bottom dishes and analyzed 72 hours after transduction. Calcium transients (Rhod2 AM) were measured at 37°C during field stimulation at 1.5 Hz to ensure consistent diastolic intervals. Images were acquired on an inverted confocal laser-scanning microscope. Transduced cells, recognized by GFP fluorescence, were randomly selected for recording of calcium transients.
Cell Area and [3H]Leucine Incorporation
For cell area measurements, NRCMs were plated in 35 mm glass-bottom dishes. Cells were serum starved for 24 hours, after which they were incubated in phenylephrine (PE). Images were acquired and cell area measurements were performed offline using Image-J software. Transduced cells were recognized by GFP fluorescence.
For [3H]leucine incorporation, 72 hours after transduction cells were incubated for 24 hours with 2µCi/mL of [3H]leucine with and without PE. Cell lysates were solubilized and the incorporated radioactivity was determined by liquid scintillation counting.
In Vivo Cardiac Gene Transfer and Aortic Banding
Adult rats were assigned to receive PPT.CG.H1.B2, PPT.CG.H1.NS, or sham intervention. After baseline echocardiographic recordings, rats were anesthetized. Lentivirus vector was injected into the LV cavity while the aorta and pulmonary artery were cross-clamped for 50 seconds. After the aorto/pulmonary cross clamp was released, the ascending aorta was banded with a 0.58 mm (internal diameter) tantalum clip as previously described.17 In sham-operated animals, 150 µL of normal saline was injected into the LV cavity while the aorta and pulmonary artery were cross-clamped for 50 seconds. In vivo transduction efficiency was assessed by X-Gal staining of PPT.CMV-LacZnls injected animals.
Quantitative Reverse-Transcription PCR
Four weeks after in vivo gene delivery, total RNA was isolated from rat hearts. For quantification of steady state mRNA levels the TaqMan gene expression assay was used. Primers and probes against the LTCCß, ß-myosin heavy chain (ß-MHC), and atrial natriuretic peptide (ANP) were designed. Quantitative PCR was performed using a 7900HT Sequence Detection System (Applied Biosystems, Foster City, Calif).
Western Blots
For Cav 1.2 expression, protein was isolated from tissue lysates as previously described.18 Samples were separated by 8% Tris-glycine SDS gel electrophoresis. Proteins were transferred to polyvinylidene sulfonyl fluoride membranes and blocked for 1 hour.A rabbit Cav1.2 antibody (Alomone Labs) was incubated overnight at 4°C. Densitometry analysis was performed to assess 
1C / tubulin ratios from sham, NS RNAi, and ß RNAi groups.
Echocardiography
Rats were anesthetized and transthoracic 2-D and M-mode images were acquired using a high-resolution 25 MHZ scan head attached to a rail system to assure standardization of imaging acquisition between animals. All images were recorded in a VisualSonics Vevo 660 high resolution rodent imaging system. Echocardiograms were performed at baseline, 2 and 4-week time points after vector transduction/aortic banding.
Invasive Blood Pressure Measurement
Blood pressure was measured invasively four weeks after aortic banding in PPT.CG.H1.ß2 and PPT.CG.H1.NS transduced animals. After rats were anesthetized, a fluid filled catheter was advanced until the aortic root (distal to the aortic band). Blood pressure was recorded and subsequently analyzed offline.
Statistics
Continuous variables are expressed as mean±standard error of the mean. Statistical analyses were performed using repeated measures ANOVA and Student paired t test, where appropriate. P<0.05 was considered to be indicative of statistical significance.
|
Results |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
In Vitro Effect of shRNA on LTCCß Expression
The gene-silencing capacity of the shRNA was initially tested in a heterologous expression system. Twenty four hours after transfection with p.LTCCß-GFP,
85% of HEK293 cells were positive for GFP fluorescence. As evidenced by fluorescent microscopy, cotransfection of PPT.H1.ß2 significantly decreased GFP expression relative to cells cotransfected with PPT.H1.NS (Figure 1B). To quantify the gene-silencing efficacy of our construct, cells were subjected to FACS analysis. In two separate experiments, PT.H1.ß2 reduced the mean fluorescence intensity of pLTCCß-GFP cotransfected cells by 64.6±7.5% compared with PPT.H1.NS cotransfected cells (Figure 1B).
Effect of LTCC ß2 Gene Suppression on Adult Cell Electrophysiology
We have recently reported that the over expression of a small G-protein (Gem) in the heart has a dramatic effect on peak ICa.19 The Gem effects on ICa are because of binding and subsequent trapping of the endogenous ß subunit.20 Accordingly we would predict that inhibition of ß subunit expression will inhibit L-type calcium current (ICa,L). To test this prediction, we measured ICa,L in adult rat ventricular cardiomyocytes. Lentiviral vector was injected into the left ventricle of rat hearts, and 5 days later cells were isolated for patch clamp studies. Only GFP positive (transduced) cells were recorded. Genetic suppression of LTCCß in transduced rat cells decreased ICa,L from a peak density of –9.31±1.52 pA/pF at 10 mV (n=11) in PPT.CG.H1.NS transduced (control, or NS RNAi) cells to –3.85±0.53 pA/pF at 10 mV (n=10) in PPT.CG.H1.B2 (ß2 RNAi, Figure 2, A and B). LTCCß gene knockdown was specific in that it did not affect another endogenous cation-selective inward current (the Na current, INa) in the ventricular myocytes; Figure 2 reveals no differences in INa between NS RNAi and ß2 RNAi groups (C and D).
|
Effects of LTCC ß2 Gene Silencing on Calcium Handling
Suppression of LTCC would be predicted to attenuate intracellular calcium cycling. For calcium transient recordings, NRCMs were transduced with either PPT.CG.H1.B2 or PPT.CG.H1.NS at a multiplicity of infection (MOI) of 50 to achieve a transduction efficiency greater than 90% by fluorescence microscopy (Figure 1C). Seventy-two hours later, calcium transient amplitude was reduced by 34% in ß2 RNAi cells (n=101) compared with NS RNAi (n=102) controls (F/Fo=8.54±0.61 versus F/Fo=13.05±0.55, P<0.01) (Figure 3).
|
Effect of LTCC ß2 Gene Knockdown on Cardiac Hypertrophy In Vitro
As a first step to investigate the role of posttranscriptional gene silencing of LTCC ß2 on cardiac hypertrophy, we used the PE-induced NRCM hypertrophy model. Seventy-two hours after transduction (MOI of 50), cells were serum-starved for 24 hours and PE stimulation was initiated. After 48 hours, cell size was 54% smaller in ß2 RNAi cells (n=53) compared with NS RNAi controls (n=56) (P<0.01) (Figure 3, D and E). Given that cultured cells can undergo changes in cell volume and area not necessarily related to the development of hypertrophy, we also measured [3H]leucine incorporation after 24 hours stimulation with PE. PE-stimulated [3H]leucine incorporation was suppressed in ß2 RNAi cells (99.3±13% of control, n=9) compared with NS RNAi cells (173.6±18% of control, n=9) (P<0.05) (Figure 3F). No differences in beating frequencies were observed between groups (data not shown), therefore ruling out an indirect effect of beat frequency on hypertrophy.
Lentiviral Vector Mediates Efficient In Vivo Gene Transfer and Knockdown of the LTCCß In Vivo
We and others have previously shown the efficacy of LV injection and aorto-pulmonary cross clamping for in vivo adenoviral vector-mediated gene delivery to the heart.21,22 Recently, advanced-generation lentiviral vectors have also been reported to efficiently transduce the rat heart by the same vector delivery technique.23 We therefore implemented a banding model of LVH in the rat and compared 3 groups: sham-operated (not-banded), ß2 RNAi, and NS RNAi groups. The transduction efficiency achieved in the current study was 50% as established by X-gal staining four weeks after injection of PPT.CMV.LacZnls (Figure 4, A and B). Four weeks after aortic banding, LTCCß2 mRNA levels were increased by 2-fold in NS RNAi (n=7) animals compared with Sham / not banded animals (n=6). Importantly, the LTCCß2 mRNA levels were reduced by 23% in ß2 RNAi rats (n=7) compared with nonsilencing controls (n=7) (Figure 4C). To assess the extent of knockdown of the LTCCß2 protein, Western blots were performed on tissue lysates and membrane preparations. Despite the use of commercial and a custom-made antibody, combined with sensitive detection systems, we were unable to achieve adequate signals from the endogenous expression of LTCCß2 in adult rat heart. As a result, quantification of LTCCß2 changes at the protein level was not possible. To rule out the possibility of an off-target effect of our RNAi, Cav1.2 protein expression was measured from tissue lysates. No changes in Cav1.2 expression were observed in Sham, NS RNAi, ß2 RNAi groups (Figure 4D).
|
In Vivo Effect of LTCC ß2 Suppression on Cardiac Hypertrophy
No significant differences in baseline characteristics were observed between the three study groups (Table). During follow up, ß2 RNAi animals exhibited an attenuated hypertrophy response compared with NS RNAi controls. Four weeks after aortic banding, left ventricular wall thickness (LVWT) was 33% smaller in ß2 RNAi rats (n=6) compared with NS RNAi controls (n=7; Figure 5, A and B, and Table). Moreover, heart weight/body weight ratios (HW/BW), were also decreased (4.55±0.16 versus 5.64±0.22, P<0.05) (Figure 5C and Table). Consistent with these findings, the mRNA levels of ß-MHC and ANP were reduced by 26% and 52% respectively in ß2 RNAi rats (n=7) compared with nonsilencing controls (n=7) (Figure 6A and B). The systemic blood pressure (distal to the aortic banding) was comparable in the NS RNAi and ß2 RNAi groups (145/88 mm Hg versus 143/89 mm Hg respectively, n=5 in each group) (Figure 6C). Thus, differences in afterload do not confound the observed changes in the hypertrophic response.
|
|
|
LTCC ß2 Knockdown Does Not Impair Systolic Performance
Downregulation of LTCCß, by affecting calcium influx and release from intracellular stores, may impair excitation-contraction coupling and systolic function. To exclude this possibility, animals were followed up to detect signs of congestive heart failure and cardiac function was studied noninvasively by high-resolution echocardiography. No signs of respiratory distress, fluid retention, or differences in body weight, ventricular heart rate were detected between groups (Figure 7, A and B and Table). Moreover, during follow-up, left ventricular diastolic diameter and shortening fraction were comparable in ß2 RNAi and NS RNAi transduced rats (Figure 7, C and D and Table). This null effect may reflect attenuation of calcium cycling pathways ordinarily upregulated in cardiac hypertrophy.24,25
|
|
Discussion |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
The fundamental role of calcium influx through the LTCC in normal excitation-contraction coupling, and the significance of calcium mishandling in heart disease, have recently been reviewed.1 The importance of the LTCC as a therapeutic target for LVH has been confirmed in many animal models that demonstrate reduction in hypertrophy by calcium channel blockers.26,27 However, there are only limited data on the effect of L-type calcium channel blockade on cardiac hypertrophy beyond blood pressure control.2,28,29 Clinically, calcium channel antagonists decrease blood pressure and induce regression of LVH, but prolongation of survival with these agents has not been demonstrated3 except in the ASCOT-BPLA trial.29 Blockade of noncardiac channels explains many of the undesired effects (eg, systemic hypotension, constipation, edema) of these agents and could also account for the dubious benefit on cardiovascular mortality. We have previously shown that genetic calcium channel blockade can be achieved in the heart, by overexpressing the small G-protein, Gem, by adenoviral gene transfer.19 Here, by incorporating a shRNA expression cassette into an "advanced" generation lentiviral vector we were able to target the LTCCß in a gene specific manner and achieve long-term modulation of cardiac calcium influx. Gene-silencing of LTCCß in NRCMs decreased calcium transients by 34%, demonstrating the importance of the endogenous levels of LTTCß for the regulation of calcium handling. In a cellular model of hypertrophy, downregulation of LTCCß expression prevented an increase in relative cell size and abrogated PE-induced protein synthesis. These in vitro findings contribute to the body of evidence supporting the key role of calcium-regulated signaling pathways in the development of cardiac hypertrophy.2
In pressure-overload conditions, enhanced calcium-regulated signaling also plays a central role in the development of LVH.2,30 Although initially considered a "compensatory" response projected to normalize wall stress and facilitate systolic performance,31 recent studies have challenged this premise.30,32 The inhibition of calcium-regulated signaling pathways has been shown to abolish pressure overload-induced LVH without compromising systolic function.32 Hence, the development of LVH is not essential for maintained systolic function in the presence of pressure overload. Conversely, suppression of hypertrophy need not undermine contractile performance. In our in vivo study system, we found an increase in: LTCCß, ß-MHC, and ANP mRNA levels 4 weeks after aortic banding. Interestingly, modulation of LTCCß attenuated the development of LVH as demonstrated by a relative decrease in LVWT and HW/BW. The reduced transcription of ANP and ß-MHC in the ß suppressive group found in our model is consistent with the changes found both in the echocardiographic and HW/BW measurements. The attenuated hypertrophic response in the setting of a "fixed" aortic constriction, together with the absence of a difference in systemic blood pressure between the nonsilencing and ß suppressive groups, support a direct cardiac effect of LTCCß knockdown independent of changes in peripheral vascular resistance.
Although a depressed cardiac contractility might be expected from LTCCß gene silencing, no changes in systolic performance, as assessed by echocardiographic shortening fraction, were detected during follow-up. Moreover, no signs of impaired cardiac performance such as respiratory distress, or fluid retention were detected. In concordance with our findings, a reduction of ICaL with preserved cardiac contractility by endogenous ß subunit trapping has previously been reported by Serikov et al in a transgenic mouse model.33 Our results may be explained by a partial reduction of LTCCß expression that is sufficient to prevent the activation of calcium-regulated signaling pathways and therefore the development of LVH, without impairing normal excitation-contraction coupling. An alternative explanation for the preservation of systolic function may relate to an antiapoptotic effect of LTCCß knockdown. Overexpression of LTCCß by adenoviral gene transfer has recently shown to induce calcium overload and apoptosis in adult feline cardiomyocytes.34 Although an antiapoptotic affect of LTCCß modulation could explain our findings further studies would need to be performed to test this hypothesis. A compensatory increase in sarcoplasmic reticulum calcium loading may also result in preserved contractility in our model.
The present strategy, associated with a vector capable of persistently modulating the expression of LTCCß may represent a novel and specific therapy for LVH and other cardiac diseases associated with calcium mishandling. Hypertrophic obstructive cardiomyopathy (HOCM), for example, is conventionally treated with pharmacological calcium channel blockers and in selected cases surgical, and more recently nonsurgical septal reduction techniques as a means of ameliorating LV outflow obstruction.35–37 However, the utility of these therapies is limited by side effects, including inflammation, fibrosis, and arrhythmogenesis. On this basis, focal modulation of LTCCß by a vector capable of chronically suppressing gene expression may represent an attractive alternative therapy in HOCM. Regional modification of endogenous LTCCß may improve outflow obstruction by nondestructively reducing septal hypertrophy without impairing global cardiac hemodynamics.
We have demonstrated that LTCCß may be modulated by RNA interference following lentiviral vector-based shRNA expression both in vitro and in vivo. The physiological consequences of this were the reduction of the ICaL and an attenuated hypertrophic response in vitro and in vivo. The latter was associated with preserved cardiac systolic function. This study system represents a novel research tool for studying calcium-regulated signaling pathways. Furthermore, these findings advocate the LTCCß as a potentially novel therapeutic target for diverse cardiac diseases associated with calcium mishandling.
Limitations
The present study serves as a proof of concept of the role of RNA interference in modulating the expression of LTCCß, regulating calcium influx and preventing LVH. Novel and less invasive gene delivery techniques will have to be developed to translate the present strategy to humans. In addition, further mechanistic studies are recquired to elucidate any potential antihypertrophic effects of LTCCß knockdown that are independent of the effects on the ICa,L.
|
Acknowledgments |
|---|
Sources of Funding
Supported by the Donald W. Reynolds Foundation. E.M. holds the Michel Mirowski, MD, Professorship of Cardiology of the Johns Hopkins University.
Disclosures
None.
|
Footnotes |
|---|
This manuscript was sent to Hans Michael Piper, Consulting Editor, for review by expert referees, editorial decision, and final disposition.
Original received December 21, 2006; resubmission received May 10, 2007; accepted May 30, 2007.
|
References |
|---|
|
TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
|---|
1. Bers DM. Cardiac excitation-contraction coupling. Nature. 2002; 415: 198–205.[CrossRef][Medline] [Order article via Infotrieve]
2. Molkentin JD, Lu JR, Antos CL, Markham B, Richardson J, Robbins J, Grant SR, Olson EN. A calcineurin–dependent transcriptional pathway for cardiac hypertrophy. Cell. 1998; 93: 215–228.[CrossRef][Medline] [Order article via Infotrieve]
3. Klingbeil AU, Schneider M, Martus P, Messerli FH, Schmieder RE. A meta-analysis of the effects of treatment on left ventricular mass in essential hypertension. Am J Med. 2003; 115: 41–46.[CrossRef][Medline] [Order article via Infotrieve]
4. Chien AJ, Zhao X, Shirokov RE, Puri TS, Chang CF, Sun D, Rios E, Hosey MM. Roles of a membrane-localized ß subunit in the formation and targeting of functional L-type Ca2+ channels. J Biol Chem. 1995; 270: 30036–30044.
5. Van Petegem F, Clark KA, Chatelain FC, Minor DL, Jr. Structure of a complex between a voltage-gated calcium channel ß-subunit and an -subunit domain. Nature. 2004; 429: 671–675.[CrossRef][Medline]
[Order article via Infotrieve]
6. Chen YH, Li MH, Zhang Y, He LL, Yamada Y, Fitzmaurice A, Shen Y, Zhang H, Tong L, Yang J. Structural basis of the 1-ß subunit interaction of voltage-gated Ca2+ channels. Nature. 2004; 429: 675–680.[CrossRef][Medline]
[Order article via Infotrieve]
7. Chien AJ, Carr KM, Shirokov RE, Rios E, Hosey MM. Identification of palmitoylation sites within the L-type calcium channel ß2a subunit and effects on channel function. J Biol Chem. 1996; 271: 26465–26468.
8. Hullin R, Khan IF, Wirtz S, Mohacsi P, Varadi G, Schwartz A, Herzig S. Cardiac L-type calcium channel ß-subunits expressed in human heart have differential effects on single channel characteristics. J Biol Chem. 2003; 278: 21623–21630.
9. Colecraft HM, Alseikhan B, Takahashi SX, Chaudhuri D, Mittman S, Yegnasubramanian V, Alvania RS, Johns DC, Marban E, Yue DT. Novel functional properties of Ca(2+) channel ß subunits revealed by their expression in adult rat heart cells. J Physiol. 2002; 541: 435–452.
10. Reynolds A, Leake D, Boese Q, Scaringe S, Marshall WS, Khvorova A. Rational siRNA design for RNA interference. Nat Biotechnol. 2004; 22: 326–330.[CrossRef][Medline] [Order article via Infotrieve]
11. Kizana E, Ginn SL, Allen DG, Ross DL, Alexander IE. Fibroblasts can be genetically modified to produce excitable cells capable of electrical coupling. Circulation. 2005; 111: 394–398.
12. Zufferey R, Donello JE, Trono D, Hope TJ. Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J Virol. 1999; 73: 2886–2892.
13. Fleming J, Ginn SL, Weinberger RP, Trahair TN, Smythe JA, Alexander IE. Adeno-associated virus and lentivirus vectors mediate efficient and sustained transduction of cultured mouse and human dorsal root ganglia sensory neurons. Hum Gene Ther. 2001; 12: 77–86.[CrossRef][Medline] [Order article via Infotrieve]
14. Akao M, Ohler A, O’Rourke B, Marban E. Mitochondrial ATP-sensitive potassium channels inhibit apoptosis induced by oxidative stress in cardiac cells. Circ Res. 2001; 88: 1267–1275.
15. Johns DC, Nuss HB, Marban E. Suppression of neuronal and cardiac transient outward currents by viral gene transfer of dominant-negative Kv4.2 constructs. J Biol Chem. 1997; 272: 31598–31603.
16. Hoppe UC, Marban E, Johns DC. Distinct gene-specific mechanisms of arrhythmia revealed by cardiac gene transfer of two long QT disease genes, HERG and KCNE1. Proc Natl Acad Sci U S A. 2001; 98: 5335–5340.
17. Del Monte F, Butler K, Boecker W, Gwathmey JK, Hajjar RJ. Novel technique of aortic banding followed by gene transfer during hypertrophy and heart failure. Physiol Genomics. 2002; 9: 49–56.
18. Ganesan AN, Maack C, Johns DC, Sidor A, O’Rourke B. ß-adrenergic stimulation of L-type Ca2+ channels in cardiac myocytes requires the distal carboxyl terminus of 1C but not serine 1928. Circ Res. 2006; 98: e11–e18.
19. Murata M, Cingolani E, McDonald AD, Donahue JK, Marban E. Creation of a genetic calcium channel blocker by targeted gem gene transfer in the heart. Circ Res. 2004; 95: 398–405.
20. Beguin P, Nagashima K, Gonoi T, Shibasaki T, Takahashi K, Kashima Y, Ozaki N, Geering K, Iwanaga T, Seino S. Regulation of Ca2+ channel expression at the cell surface by the small G-protein kir/Gem. Nature. 2001; 411: 701–706.[CrossRef][Medline] [Order article via Infotrieve]
21. Miake J, Marban E, Nuss HB. Functional role of inward rectifier current in heart probed by Kir2.1 overexpression and dominant-negative suppression. J Clin Invest. 2003; 111: 1529–1536.[CrossRef][Medline] [Order article via Infotrieve]
22. del Monte F, Hajjar RJ. Efficient viral gene transfer to rodent hearts in vivo. Methods Mol Biol. 2003; 219: 179–193.[Medline] [Order article via Infotrieve]
23. Bonci D, Cittadini A, Latronico MV, Borello U, Aycock JK, Drusco A, Innocenzi A, Follenzi A, Lavitrano M, Monti MG, Ross J Jr, Naldini L, Peschle C, Cossu G, Condorelli G. ‘Advanced’ generation lentiviruses as efficient vectors for cardiomyocyte gene transduction in vitro and in vivo. Gene Ther. 2003; 10: 630–636.[CrossRef][Medline] [Order article via Infotrieve]
24. Carvalho BM, Bassani RA, Franchini KG, Bassani JW. Enhanced calcium mobilization in rat ventricular myocytes during the onset of pressure overload-induced hypertrophy. Am J Physiol Heart Circ Physiol. 2006; 291: H1803–H1813.
25. Fowler MR, Naz JR, Graham MD, Bru-Mercier G, Harrison SM, Orchard CH. Decreased Ca2+ extrusion via Na+/Ca2+ exchange in epicardial left ventricular myocytes during compensated hypertrophy. Am J Physiol Heart Circ Physiol. 2005; 288: H2431–H2438.
26. Richard S, Leclercq F, Lemaire S, Piot C, Nargeot J. Ca2+ currents in compensated hypertrophy and heart failure. Cardiovasc Res. 1998; 37: 300–311.
27. Feron O, Salomone S, Godfraind T. Action of the calcium channel blocker lacidipine on cardiac hypertrophy and endothelin-1 gene expression in stroke-prone hypertensive rats. Br J Pharmacol. 1996; 118: 659–664.[Medline] [Order article via Infotrieve]
28. Lubic SP, Giacomini KM, Giacomini JC. The effects of modulation of calcium influx through the voltage-sensitive calcium channel on cardiomyocyte hypertrophy. J Mol Cell Cardiol. 1995; 27: 917–925.[CrossRef][Medline] [Order article via Infotrieve]
29. Dahlof B, Sever PS, Poulter NR, Wedel H, Beevers DG, Caulfield M, Collins R, Kjeldsen SE, Kristinsson A, McInnes GT, Mehlsen J, Nieminen M, O’Brien E, Ostergren J. Prevention of cardiovascular events with an antihypertensive regimen of amlodipine adding perindopril as required versus atenolol adding bendroflumethiazide as required, in the Anglo-Scandinavian Cardiac Outcomes Trial-Blood Pressure Lowering Arm (ASCOT-BPLA): a multicentre randomised controlled trial. Lancet. 2005; 366: 895–906.[CrossRef][Medline] [Order article via Infotrieve]
30. Hill JA, Karimi M, Kutschke W, Davisson RL, Zimmerman K, Wang Z, Kerber RE, Weiss RM. Cardiac hypertrophy is not a required compensatory response to short-term pressure overload. Circulation. 2000; 101: 2863–2869.
31. Grossman W, Jones D, McLaurin LP. Wall stress and patterns of hypertrophy in the human left ventricle. J Clin Invest. 1975; 56: 56–64.[Medline] [Order article via Infotrieve]
32. Esposito G, Rapacciuolo A, Naga Prasad SV, Takaoka H, Thomas SA, Koch WJ, Rockman HA. Genetic alterations that inhibit in vivo pressure-overload hypertrophy prevent cardiac dysfunction despite increased wall stress. Circulation. 2002; 105: 85–92.
33. Serikov V, Bodi I, Koch SE, Muth JN, Mikala G, Martinov SG, Haase H, Schwartz A. Mice with cardiac-specific sequestration of the ß-subunit of the L-type calcium channel. Biochem Biophys Res Commun. 2002; 293: 1405–1411.[CrossRef][Medline] [Order article via Infotrieve]
34. Chen X, Zhang X, Kubo H, Harris DM, Mills GD, Moyer J, Berretta R, Potts ST, Marsh JD, Houser SR. Ca2+ influx-induced sarcoplasmic reticulum Ca2+ overload causes mitochondrial-dependent apoptosis in ventricular myocytes. Circ Res. 2005; 97: 1009–1017.
35. Nielsen CD, Spencer WH, 3rd. Role of controlled septal infarct in hypertrophic obstructive cardiomyopathy. Cardiol Rev. 2002; 10: 108–118.[CrossRef][Medline] [Order article via Infotrieve]
36. Sigwart U. Non-surgical myocardial reduction for hypertrophic obstructive cardiomyopathy. Lancet. 1995; 346: 211–214.[CrossRef][Medline] [Order article via Infotrieve]
37. Chang SM, Nagueh SF, Spencer WH, 3rd, Lakkis NM. Complete heart block: determinants and clinical impact in patients with hypertrophic obstructive cardiomyopathy undergoing nonsurgical septal reduction therapy. J Am Coll Cardiol. 2003; 42: 296–300.
This article has been cited by other articles:
 |
|
 |
|
  N. Beetz, L. Hein, J. Meszaros, R. Gilsbach, F. Barreto, M. Meissner, U. C. Hoppe, A. Schwartz, S. Herzig, and J. Matthes Transgenic simulation of human heart failure-like L-type Ca2+-channels: implications for fibrosis and heart rate in mice Cardiovasc Res, December 1, 2009; 84(3): 396 - 406. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 C.-S. Chiang, C.-H. Huang, H. Chieng, Y.-T. Chang, D. Chang, J.-J. Chen, Y.-C. Chen, Y.-H. Chen, H.-S. Shin, K. P. Campbell, et al. The CaV3.2 T-Type Ca2+ Channel Is Required for Pressure Overload-Induced Cardiac Hypertrophy in Mice Circ. Res., February 27, 2009; 104(4): 522 - 530. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. Telemaque, S. Sonkusare, T. Grain, S. W. Rhee, J. R. Stimers, N. J. Rusch, and J. D. Marsh Design of Mutant {beta}2 Subunits as Decoy Molecules to Reduce the Expression of Functional Ca2+ Channels in Cardiac Cells J. Pharmacol. Exp. Ther., April 1, 2008; 325(1): 37 - 46. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 H. Wang, M. J. Kohr, D. G. Wheeler, and M. T. Ziolo Endothelial nitric oxide synthase decreases {beta}-adrenergic responsiveness via inhibition of the L-type Ca2+ current Am J Physiol Heart Circ Physiol, March 1, 2008; 294(3): H1473 - H1480. [Abstract] [Full Text] [PDF]
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||