Sympathetic neurons are a powerful driver of myocyte function in cardiovascular disease

ABSTRACT Many therapeutic interventions in disease states of heightened cardiac sympathetic activity are targeted to the myocytes. However, emerging clinical data highlights a dominant role

in disease progression by the neurons themselves. Here we describe a novel experimental model of the peripheral neuro-cardiac axis to study the neuron’s ability to drive a myocyte cAMP

phenotype. We employed a co-culture of neonatal ventricular myocytes and sympathetic stellate neurons from normal (WKY) and pro-hypertensive (SHR) rats that are sympathetically

hyper-responsive and measured nicotine evoked cAMP responses in the myocytes using a fourth generation FRET cAMP sensor. We demonstrated the dominant role of neurons in driving the myocyte

ß-adrenergic phenotype, where SHR cultures elicited heightened myocyte cAMP responses during neural activation. Moreover, cross-culturing healthy neurons onto diseased myocytes rescued the

diseased cAMP response of the myocyte. Conversely, healthy myocytes developed a diseased cAMP response if diseased neurons were introduced. Our results provide evidence for a dominant role

played by the neuron in driving the adrenergic phenotype seen in cardiovascular disease. We also highlight the potential of using healthy neurons to turn down the gain of neurotransmission,

akin to a smart pre-synaptic ß-blocker. SIMILAR CONTENT BEING VIEWED BY OTHERS MYOCARDIAL TRPC6-MEDIATED ZN2+ INFLUX INDUCES BENEFICIAL POSITIVE INOTROPY THROUGH Β-ADRENOCEPTORS Article Open

access 26 October 2022 SELECTIVE INDUCTION OF HUMAN AUTONOMIC NEURONS ENABLES PRECISE CONTROL OF CARDIOMYOCYTE BEATING Article Open access 11 June 2020 VAGUS NERVE STIMULATION OPTIMIZED

CARDIOMYOCYTE PHENOTYPE, SARCOMERE ORGANIZATION AND ENERGY METABOLISM IN INFARCTED HEART THROUGH FOXO3A-VEGF SIGNALING Article Open access 12 November 2020 INTRODUCTION Many therapeutic

interventions in states of heightened adrenergic activity associated with cardiovascular disease are targeted at the myocyte, suggesting these cells are of primary importance in driving the

disease process1,2. However, emerging clinical evidence suggests that removal of sympathetic nerves that innervate the heart (cardiac stellectomy) improves morbidity and mortality caused by

arrhythmias and sudden cardiac death3, although the ability of the neuron to drive the myocyte phenotype in disease has not been firmly established. Nevertheless cardiac sympathetic

hyperactivity is a well established early hallmark of heart failure4,5, post myocardial infarction6 and hypertension, both in humans7,8,9,10,11 and in the spontaneously hypertensive rat

(SHR)12,13. In the pro-hypertensive SHR, the sympathetic stellate neurons that predominantly innervate the heart14 show increased membrane Ca2+ currents15,16, intracellular Ca2+ transients17

and significant impairment of the noradrenaline reuptake transporter (NET)18 that all contribute to enhanced noradrenaline (NA) release13,19,20. This heightened sympathetic activity at the

end organ results in ß-adrenergic hyper-responsiveness of the myocyte21,22,23. In addition, sino-atrial cells21 and ventricular myocytes22 from the SHR also display increased basal and

stimulated heart rate13,19, linked to significantly greater basal and NA stimulated L-type Ca2+ currents21,22. Since the disease phenotype resides in two spatial domains, the relative

contribution each makes to dysautonomia remains unclear, even though the (patho-) physiology of the individual ion channels and signalling molecules on the single neuron and single myocytes

as separate systems are well described. Surprisingly relatively little is known about the cell-to-cell interaction that takes place in disease24,25. What is now becoming clear is that

sympathetic neurons play a larger role in modulating the behaviour of myocytes than previously thought8,26,27. This occurs both via anterograde signalling28, but also through eliciting

changes in the expression of ion channels and receptors on the myocyte membrane that are critically involved in myocyte function29,30,31, and more recently, through changes in the structure

of the neuro-cardiac junction31,32. To fully understand the importance of sympathetic neurotransmission on end-organ function and how it might be altered in disease28, we developed a model

system to study the peripheral neuro-cardiac axis itself, rather than the cells in isolation. We also used a novel cAMP FRET (Förster Resonance Energy Transfer) sensor to measure post

synaptic sympathetic drive when we cross-cultured normal neurons onto diseased myocytes and vice versa as we attempted to modulate the myocyte phenotype. Here we addressed the following

questions: (i) does sympathetic hyperactivity observed in the single neuron and single myocyte, translate into a native co-culture of functionally coupled sympathetic stellate neurons and

ventricular myocytes? (ii) Is the neuron or the myocyte the primary driver of the cardiac adrenergic phenotype associated with the pro-hypertensive state? RESULTS THE CO-CULTURE PHENOTYPE

AND CROSS-CULTURE FORMATION The myocytes were densely innervated by the sympathetic neurons (Fig. 1a), analogous to that observed _in vivo_33. Immunofluorescence confirmed the cellular

phenotypes with sarcomeric alpha-actinin denoting the myocytes, and tyrosine hydroxylase (TH) denoting the sympathetic neurons. The sympathetic neurons displayed the characteristic punctate

staining of the varicosities, indicative of sites of synapse formation28,34 (Fig. 1a). Visual innervation was observed in all cultures that were recorded from. The cross-culture formation is

detailed in Fig. 1b. The was no visual difference in the appearance of the WKYnSHRm or the SHRnWKYm when compared to the WKYnWKYm and SHRnSHRm (24, 42, 60 and 102 images respectively – data

not shown). THE MYOCYTES FROM THE PRO-HYPERTENSIVE SHR ARE OVER-RESPONSIVE TO BETA ADRENERGIC STIMULATION To test the ß-adrenergic responsiveness of the myocytes, we bath applied the

ß-agonist isoprenaline and measured the changes in cAMP levels using FRET. Isoprenaline treatment of the myocytes revealed that the SHR myocytes were significantly hyper-responsive when

compared to the WKY myocytes at isoprenaline concentrations ≥3 nM (Fig. 2). The responses increased over the concentrations tested and plateaued between 30 nM and 100 nM. THE CO-CULTURES

FROM THE PRO-HYPERTENSIVE SHR (SHRNSHRM) ARE HYPER-RESPONSIVE TO NICOTINIC ACTIVATION Following the addition of nicotine to the co-culture, myocyte cAMP levels increased rapidly before

returning to baseline confirming that the two cells were functionally connected. The myocytes from the pro-hypertensive SHRnSHRm co-cultures showed significantly larger nicotine-evoked cAMP

responses when compared to the WKYnWKYm at 1 μM (55.89 ± 7.292%, n = 28 vs 5.952 ± 1.623%, n = 24, p < 0.0001) and 10 μM (44.02 ± 5.310%, n = 36 vs 17.05 ± 3.715%, n = 29, p < 0.0002)

nicotine (see Fig. 3b,c). At 100 μM the responses of the two co-cultures were the same (38.25 ± 6.105%, n = 20 vs 39.35 ± 3.283%, n = 27, p = 0.87. Figure 3d). At the higher concentrations

of nicotine (300 and 500 μM), significantly reduced responses were found in both co-cultures that were not significantly different from each other (results not shown). Both co-cultures

responded identically to maximal activation of the sensor with 100 μM IBMX (a general phosphodiesterase - PDE - inhibitor) and 25 μM forskolin (WKY: 241.2 ± 5.94% n = 76 cells. SHR: 239.0 ± 

5.74% n = 87 cells, p = 0.79). Furthermore, roughly half of the SHRnSHRm co-cultures portrayed double peaks (see arrow on Fig. 3d) of cAMP elevation. This double peak behaviour was not

observed in any of the WKYnWKYm co-cultures. MYOCYTE CAMP RESPONSES IN THE CO-CULTURES ARE MEDIATED BY THE Β1 ADRENERGIC RECEPTOR. The application of the β1 selective antagonist metoprolol

(10 μM) blocked all nicotine evoked cAMP responses (Fig. 4a) in the SHRnSHRm and WKYnWKYm co-cultures at all nicotine concentration and in all cells tested (n = 60 cells). To confirm the

absence of contaminating intra-cardiac neurons in the myocytes culture, we tested the cAMP response to nicotine, and performed immunofluorescence on myocytes culture alone. Nicotine

application (1–500 μM) to the myocytes did not change cAMP levels in any cells tested (WKY n = 9, SHR n = 20 cells) (Fig. 4b). Immunofluorescence staining for tyrosine hydroxylase (TH) and

choline acetyltransferase (ChAT) confirmed the absence of sympathetic or parasympathetic intra-cardiac neurons in the myocytes cultured alone (Fig. 4c). ARE THE CARDIAC SYMPATHETIC STELLATE

NEURONS THE PRINCIPLE DRIVERS BEHIND THE CARDIAC AUTONOMIC DYSFUNCTION ASSOCIATED WITH THE PRO-HYPERTENSIVE STATE? To test the role played by the sympathetic neurons in the cardiac

sympathetic hyper-activity, the nicotine-evoked cAMP responses of the cross-cultures (WKYnSHRm and SHRnWKYm were compared to the WKYnWKYm and SHRnSHRm co-cultures. We found that in the

WKYnSHRm cross-cultures (Fig. 5b), the normal WKY neurons rescued the cAMP responses of the pro-hypertensive SHR myocytes (Fig. 5c,d). The nicotine-evoked cAMP responses of the myocytes in

the WKYnSHRm were significantly smaller than those from the SHRnSHRm (15.67 ± 1.936%, n = 24 vs 44.02 ± 5.310%, n = 36, p < 0.0001) and not significantly different from that of the

WKYnWKYm cultures (15.67 ± 1.936%, n = 24 vs 17.05 ± 3.715%, n = 29, p = 0.757). Further, in the SHRnWKYm cross-culture (Fig. 5e), the pro-hypertensive SHR neurons were able to induce induce

a ‘diseased’ cAMP response in the otherwise healthy WKY myocytes (Fig. 5f,g). The nicotine-evoked cAMP responses of the myocytes from the SHRnWKYm culture were substantially (though not

significantly) larger than those of the WKYnWKYm culture. However, this response was not statistically different from those of the diseased SHRnSHRm culture (31.37 ± 5.194%, n = 42 vs 44.02 

± 5.310%, n = 36, p = 0.094), indicating the diseased neurons had partially recapitulated the SHRnSHRm cAMP phenotype. DISCUSSION The novel findings presented here are: (i) the cardiac

sympathetic dysfunction identified in the single diseased neuron and myocyte translates into coupled co-cultures; (ii) the myocytes of the pro-hypertensive SHRs have an enhanced cAMP

response to ß-adrenergic stimulation; (iii) cross-culturing healthy neurons onto diseased myocytes rescues the myocyte phenotype. Conversely, healthy myocytes can develop a diseased

phenotype if diseased neurons are introduced, suggesting the neurons are the dominant drivers behind the sympathetic phenotype in pro-hypertensive states. The SHRnSHRm co-culture showed

significantly elevated myocyte cAMP responses when compared to the WKYnWKYm culture. Interestingly the response to nicotine was consistently elevated in the SHRnSHRm co-cultures, but had a

graded appearance in the WKYnWKYm cultures, both reaching a maximum at 100 μM nicotine (Fig. 3e). This could suggest differential sensitivity to nicotine with a potentially larger amount of

NA being released per unit of nicotine. This is aligned with the large body of evidence in both human9,35,36 and animal models13,15,20 of hypertension showing increased NA release. It is

clear that both the vascular bed and the heart of SHRs have significantly higher expression of nerve growth factor (NGF)37. As such, it is conceivable that increased NGF expression could

result in increased innervation25,38 in the SHR animals, since hyper-innervation has been demonstrated in the stroke-prone SHRs both prior to, and after the development of hypertension39.

This was postulated to be caused by hyperactivity of the stellate ganglion and could help explain the increased incidence of arrhythmias associated with hypertension40,41. However, over

excitability of the myocytes themselves could also play a part. Indeed, when exposed to increasing concentrations of the ß-adrenergic agonist isoprenaline (0.1–100 nM), the SHR myocytes

generated significantly larger cAMP responses when compared to the WKY controls at concentrations ≥ 3 nM (Fig. 2). This is consistent with previous reports demonstrating ß-adrenergic

over-activity associated with the hypertensive state19,21,22,42,43. This was linked to larger basal- and ß-adrenoreceptor stimulated L-type Ca2+ currents in pacemaking cells21 and

ventricular myocytes22. The latter may contribute to the increased arrhythmogenic actions of isoprenaline23. A study assessing myocardial adrenoreceptors and adenylate cyclase (AC) activity

in the developing pro-hypertensive SHRs (0–125 days post birth) demonstrated that whilst ß-adrenergic receptor expression was unchanged between the pro-SHR and WKY, a significant increase in

the isoprenaline- and forskolin-induced activity of AC was identified in SHR myocytes42. Consistent with that work, a more recent study confirmed these findings and identified significantly

increased chronotropic responses of neonatal SHR myocytes to isoprenaline43. This could explain the increased isoprenaline-induced cAMP responses of the neonatal SHR myocytes seen in our

study. Moreover, plating un-cultured thoracolumbar explants of the SHR onto WKY myocytes supports the notion the myocyte is the dominant driver2, although these neurons do not solely

innervate the heart and could be contaminated by preganglionic, acetylcholine releasing cells. Interestingly, the increased heart rate responses to isoprenaline are only present in adult

animals with established hypertension19,21, and not in the pro-hypertensive four-week old animals13, in contrast to the sympathetic phenotype17. Intriguingly, the increased heart rate

responsiveness is correlated with the development of increased sympathetic drive17 which could suggest that the ß-adrenergic hyper-activity comes about as a result of neuronal dysfunction10.

Our results are not consistent with the myocyte being the dominant driver. Given the persistent differences of the myocyte response to isoprenaline at the higher, un-physiological

concentrations, one would expect the nicotine-evoked responses of the co-cultures to stay different and not reach a common maximum. Is it possible that a more dominant role is played by the

sympathetic neuron, and that the neuronal response to autonomic stimulation takes precedence over any myocyte phenotype? To test this, we developed two cross-cultures; the WKYnSHRm and the

SHRnWKYm and exposed them to the same experimental protocol as the WKYnWKYm and SHRnSHRm. To prevent the risk of false negatives due to under-stimulation of the WKYnWKYm co-cultures, and to

maximise the chance of resolving the cross-culture phenotypes, 10 μM nicotine was chosen for the cross-culture studies. At this concentration there were clear nicotine evoked cAMP responses

from all co-cultures and a significant pro-hypertensive phenotype present in the SHRnSHRm co-cultures. We found that in the WKYnSHRm cross-culture, the normotensive neuron was able to

attenuate the elevated cAMP responses in the SHR myocyte, to similar levels to the WKYnWKYm co-cultures (Fig. 5c,d). Moreover, in the SHRnWKYm cross-culture the pro-hypertensive neurons were

able to induce a diseased cAMP phenotype in the otherwise healthy WKY myocytes (Fig. 5f,g). Together these results demonstrate that neurons are the principle drivers of post synaptic

excitability in this model of cardiac sympathetic hyper-responsiveness associated with the pro-hypertensive state, and support mounting evidence from our laboratory13,15,17 and

others7,8,9,10,27,44,45,46 that neurons may play a more dominant role than previously thought. The precise mechanism whereby the healthy neuron protects the diseased myocyte is not fully

established, but is probably related to the neuron releasing less transmitter for a given depolarisation. What is the molecular mechanism of the neuronal hyper-responsiveness? The data

provided here suggest that altered NA release from the sympathetic neuron could account for the differences seen between the WKYnWKYm and SHRnSHRm and its reversal in the cross-cultures

since responses were blocked by metoprolol. Indeed, plasma NA levels form an important prognostic marker in the development of hypertension and heart failure9,10,28,47 and an indicator of

overall mortality10. The exact mechanisms behind this also remains unclear, in part due to difficulties in accurately measuring local NA release9,48,49. Early work demonstrated that

acetylcholine-induced currents in postganglionic sympathetic neurons had similar properties between the SHR and WKY rats50, suggesting that the autonomic phenotype is unlikely to be present

at the level of the nicotinic acetylcholine receptor (nAChR). More recent work has demonstrated significantly altered Ca2+ handling in the sympathetic neurons of the pro-SHR, manifested in

both increased intracellular Ca2+ transients17 and membrane N-type currents15 – both facilitating increased neurotransmission13. Emerging evidence suggests oxidative stress leading to

dysregulation of cyclic nucleotide signalling plays a major role behind the elevated Ca2+. These neurons show impaired nitric oxide (NO) - cGMP signalling resulting in lower cGMP levels and

disinhibition of neurotransmission51,52,53,54. Moreover we recently reported that the neuronal Ca2+ channel phenotype in the SHR is linked to a phosphodiesterase – cyclic nucleotide

impairment and failure of cGMP signalling to inhibit ICaN16. The neuro-cardiac synapse is a highly specialised zone28,31,55,56,57 that is structurally dependent on the activity of the

sympathetic neurons31. The activity-dependence of such processes could have significant relevance to conditions of autonomic imbalance such as hypertension and heart failure since emerging

evidence suggests the early hallmarks of the disease appear to present themselves in the nervous system13,15,17. Whether these conditions are associated with molecular remodelling of the

synaptic space in the early evolution of the disease process has not been firmly established. In conclusion, our results provide some of the first direct evidence for the dominant role

played by the neuron in the initiation and/or maintenance of cardiac sympathetic hyperactivity. We also highlight the potential of developing cell therapies targeted at the post ganglionic,

presynaptic neuron to turn down the gain of neurotransmission, akin to a smart pre-synaptic ß-blocker. METHODS ANIMAL MODELS In this study the spontaneously hypertensive rat (SHR) and its

normotensive genetic controls, Wistar Kyoto (WKY) were used, since it has a well established autonomic phenotype at all levels of the cardiac neural axis13,17,21,39,42,58. The SHR begins to

show development of clinical symptoms of hypertension from six week of age. All experiments were approved by Oxford University’s Animal Ethics Committee and carried out in accordance with

the UK Home Office Animals Scientific Procedures Act, 1986 (PPL 30/3131, David J. Paterson). CO-CULTURE OF SYMPATHETIC STELLATE NEURONS AND VENTRICULAR MYOCYTES MYOCYTE ISOLATION Neonatal

ventricular myocytes (P3) from SHR and WKY littermates were isolated by enzymatic digestions. Briefly, the hearts were removed and atria discarded to prevent the presence of potentially

contaminating intra-cardiac ganglions. The ventricles were cut into ~3 mm3 pieces and washed with ice cold Hanks Balanced Salt Solution (HBSS) before being enzymatically digested in a

trypsin solution (1 mg/ml in HBSS) rotating at 4 °C for four hours. A series of six, two-minute collagenase (1 mg/ml) digestions in a 37 °C water bath followed. The supernatant from the

first round of the collagenase was discarded without disrupting the cells. A further five, two minute incubations in collagenase was completed. After each one, the tissue was titrated 15

times (one/second) using a wide bored (~4 mm diameter) plastic pipette to release single cells. The supernatant containing the cells was placed in cold HBSS before more enzyme was added to

the tissues and the digestions continued. The resulting single cell suspension was filtered through a 40 μm filter (EASYstrainer, Greiner bio-one, UK) to remove any cell clusters before the

cells were centrifuged at 1000 revolutions per minute for eight minutes to pellet the cells. The pellet was re-suspended in five mL of myocyte plating media and placed into two 35 mm

non-coated petri dishes and pre-plated for one hour to remove fibroblasts at 37 °C, 5% CO2. Approximately 78 000 cells were plated per four-well plate, each containing four, six mm

coverslips coated with Poly-D-Lysine and laminin. This left room for the neurons to sit down in-between the myocytes and achieved a 75% confluent cell layer at day five. The myocyte-only

cultures were plated in myocyte media (17% M199, 68% DMEM, 5% fetal bovine serum, 10% horse serum, 1% Penicillin/streptomycin), whilst the myocyte cultures awaiting neurons were plated in

co-culture media (myocyte media + 50 ng/ml nerve growth factor, 2.5 S, Millipore). CARDIAC SYMPATHETIC NEURON ISOLATION The sympathetic stellate neurons were isolated as described in18.

Briefly, the right and left stellate ganglion were removed from four-week old male pro-hypertensive SHR and normotensive WKY rats. The ganglia were desheathed before being subjected to a

series of collagenase (1 mg/ml) and trypsin (2 mg/ml) at 37 °C and triturated to achieve single cell suspension. CO-CULTURE AND CROSS CULTURE FORMATION AND NOMENCLATURE Immediately following

their culture, the neurons were placed on top of the myocytes to create the normotensive co-culture (WKYnWKYm) and the hypertensive co-culture (SHRnSHRm). The cross-cultures were created by

plating WKY neurons on SHR myocytes (WKYnSHRm), and plating SHR neurons on WKY myocytes (SHRnWKYm). The cells were left to settle for 24 hours at 37 °C, 5% CO2 before cytosine arabinoside

(1 μM) was added to eliminate fibroblast growth. The cultures were maintained for five days to allow synaptic connections to form between the cells59. All cultures were exposed to identical

experimental protocols and care was taken to ensure the myocytes were innervated by a single neuron. Supplementary video S1 depicts a WKYnWKYm culture on day five post culture.

IMMUNOFLUORESCENCE Immunofluorescence was performed to confirm myocyte and sympathetic neuron phenotypes and to ensure the absence of cholinergic neurons. Cultures were fixed in 4%

paraformaldehyde for 10 minutes before being permeabilised and blocked for one hour using a solution containing 10% goat serum, 0.3% bovine serum albumin and 0.1% Triton X in PBS. Primary

antibodies to sarcomeric alpha actinin (myocyte marker, A7811, 1:650) and tyrosine hydroxylase (sympathetic neuron marker, ab152, Abcam, 1:250) and choline acetyl transferase (cholinergic

neuron marker, ab144P, Abcam, 1:500) were incubated over night at 4 °C. Alexafluor conjugated antibodies were incubated for two hours before the coverslips were washed and mounted using a

DAPI containing soft mount Vectashield (Vectorlabs). Imaging was done using a Live Cell Olympus confocal microscope. IMAGING OF THE CULTURE USING FÖRSTER RESONANCE ENERGY TRANSFER (FRET)

IMAGING The generation of cAMP in the myocytes in response to receptor activation was assayed using a novel adenoviral cAMP FRET sensor, Ad-Epac-SH187 16 as a measure of adrenergic drive in

the myocyte. INFECTION OF THE FRET SENSOR The myocytes were selectively infected with Ad-Epac-SH187. 3.6 × 105 particle forming units (PFUs) were added for three hours at 37 °C, 5% CO2

before the media was replaced and the cells placed back into the incubator. The cells were left for 24 hours before imaging to allow for adequate expression of the FRET sensor60. FRET

IMAGING OF CULTURES The cultures were perfused with tyrode solution (in mM; 135 NaCl, 4.5 KCl, 11 glucose, 20 HEPES, 1MgCl2, 2 CaCl2, pH 7.40 - containing drugs when appropriate) at 2.5 

ml/min and imaged using an inverted Nikon microscope connected to an OptoLED fluorescence imaging system (Cairn Research Ltd) equipped with a 40x oil-immersion objective, a CoolSnap HQ2

digital CCD camera (Photometics) and a beam-splitter (DV2, Photometrics) which included the emission filters for CFP and YFP acquisition (dichroic mirror 505DCXR). The cells were excited at

430 nm and CFP and YFP emissions were measured as a change in the ratio between 480/535 nm fluorescent emission intensities following a 100 ms excitation at 430 nm, every 15 seconds.

Background fluorescence was subtracted from emission intensities and intensity ratios were plotted against time. Mean FRET responses were expressed as the percentage change from baseline

(∆R/R0 where ∆R = R-R0. R0 is the ratio of intensity at time = 0 seconds and R is the ratio at time = t seconds)60. FRET PROTOCOLS The co-cultures were stimulated with different

concentrations (1, 10, 100, 300 and 500 μM) of nicotine to physiologically activate the neuron. The cells were perfused with tyrode solution for two minutes to ensure a stable baseline

before nicotine was applied. Each culture was exposed to one concentration of nicotine, to prevent confounding results due to the inactivation of the nicotinic receptor. To test whether the

responses observed were β1 adrenoreceptor mediated, the cultures were pre-incubated with the selective β1 receptor antagonist metoprolol (10 μM) for four minutes before nicotine was added.

The myocyte-only cultures were exposed to either 0.1, 3 and 30 or 1, 10 and 100 nM isoprenaline to test their sensitivity to β1 adrenergic stimulation. Further, they were exposed to 1–500 μM

nicotine to ensure nicotine had no non-specific effect on cAMP levels in myocytes cultured alone, and to confirm the absence of any contaminating intra-cardiac neurons. STATISTICAL ANALYSIS

AND FIGURE PREPARATION Data are represented as the mean (±SEM) raw FRET ratios of all data traces. The absolute peak values were expressed as %FRET change from baseline and it was these

data the statistical analysis were performed on. All data were found to be normally distributed. Two-way ANOVA with Bonferroni correction was used for the isoprenaline dose-response data in

Fig. 2. Unpaired t-tests were used to compare the mean absolute peak values for the nicotine responses in Fig. 3. One-way ANOVA with Bonferroni correction was used to analyse the

cross-cultures in Fig. 5. Statistical significance was accepted at p values < 0.05. For each co-culture, 2–3 separate isolations were performed with 6–15 pups. Figures 1b and 5b and e

were created using Servier Medical Art according to a Creative Commons Attribution 3.0 Unported License guidelines 3.0 (https://creativecommons.org/licenses/by/3.0/). Simplification and

colour changes were made to the original neuron and mycoyte cartoons. ADDITIONAL INFORMATION HOW TO CITE THIS ARTICLE: Larsen, H. E. _et al_. Sympathetic neurons are a powerful driver of

myocyte function in cardiovascular disease. _Sci. Rep._ 6, 38898; doi: 10.1038/srep38898 (2016). PUBLISHER'S NOTE: Springer Nature remains neutral with regard to jurisdictional claims

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FRET-based reporters. Methods Mol. Biol. 1294, 1–12 (2015). CAS  PubMed  Google Scholar  Download references ACKNOWLEDGEMENTS This work was supported by a Wellcome Trust OXION D.Phil grant

to HEL and the British Heart Foundation Centre of Research Excellence. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * OXION Initiative in Ion Channels and Disease, Sherrington Building,

University of Oxford, Oxford, OX1 3PT, UK Hege E. Larsen & David J. Paterson * Department of Physiology, Burdon Sanderson Cardiac Science Centre, Anatomy and Genetics, University of

Oxford, UK Hege E. Larsen, Konstantinos Lefkimmiatis & David J. Paterson Authors * Hege E. Larsen View author publications You can also search for this author inPubMed Google Scholar *

Konstantinos Lefkimmiatis View author publications You can also search for this author inPubMed Google Scholar * David J. Paterson View author publications You can also search for this

author inPubMed Google Scholar CONTRIBUTIONS H.E.L., D.J.P. and K.L. designed the experiments and co-wrote the paper. H.E.L. performed all experiments and analysed the data. K.L. provided

the FRET sensor. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing financial interests. ELECTRONIC SUPPLEMENTARY MATERIAL SUPPLEMENTARY VIDEO S1 SUPPLEMENTARY

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CITE THIS ARTICLE Larsen, H., Lefkimmiatis, K. & Paterson, D. Sympathetic neurons are a powerful driver of myocyte function in cardiovascular disease. _Sci Rep_ 6, 38898 (2016).

https://doi.org/10.1038/srep38898 Download citation * Received: 16 June 2016 * Accepted: 15 November 2016 * Published: 14 December 2016 * DOI: https://doi.org/10.1038/srep38898 SHARE THIS

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