Abstract
The mechanisms that facilitate animal magnetoreception have both fascinated and confounded scientists for decades, and its precise biophysical origin remains unclear. Among the proposed primary magnetic sensors is the flavoprotein, cryptochrome, which is thought to provide geomagnetic information via a quantum effect in a light-initiated radical pair reaction. Despite recent advances in the radical pair model of magnetoreception from theoretical, molecular and animal behaviour studies, very little is known of a possible signal transduction mechanism. We report a substantial effect of magnetic field exposure on seizure response in Drosophila larvae. The effect is dependent on cryptochrome, the presence and wavelength of light and is blocked by prior ingestion of typical antiepileptic drugs. These data are consistent with a magnetically-sensitive, photochemical radical pair reaction in cryptochrome that alters levels of neuronal excitation, and represent a vital step forward in our understanding of the signal transduction mechanism involved in animal magnetoreception.
Many animals sense the Earth's magnetic field. Of the proposed biophysical mechanisms, the best described are a magnetite-based system1,2 and chemical magnetoreception based on a photoinitiated radical pair reaction3,4. Both have credible experimental and theoretical foundations, and may not be mutually exclusive. Much of the behavioural work in this area has been conducted using complex animals that migrate (e.g. species of bird, turtle and lobster)5. However, simpler animals that don't migrate, including the fruit fly Drosophila melanogaster6,7,8,9,10, also possess a magnetic sense. This significantly broadens the type of biophysical, neurobiological and genetic investigation available to establish primary receptor mechanism and signal transduction. The magnetic sense of Drosophila is dependent on the presence of the flavin adenine dinucleotide (FAD)-containing, circadian clock photoreceptor protein, cryptochrome (DmCRY)7, and the presence and wavelength of light to which the flies are exposed6,7,8,9. CRY are closely related to the light-dependent DNA repair enzymes, the photolyases. A second, UV-harvesting pterin chromophore is also present in members of the CRY/photolyase family, but the residues involved in binding differ significantly in DmCRY such that pterin-binding is thought unlikely11,12,13. CRY-dependent magnetoreception is currently proposed to be a result of light-initiated electron transfer chemistry in the protein, which is magnetically-sensitive by virtue of the radical pair mechanism3,4. Spin correlated radical pairs can undergo coherent mixing between singlet and triplet spin states, which have different reactive fates, and this mixing process can be modulated by magnetic fields14,15. The exact identity of the magnetically-sensitive radical pair in CRY is currently unknown. Presumably the influence of the magnetic field in some way affects the concentration of a CRY signalling state that, in turn, results in a neurophysiological response. However, there exists very little evidence of the signal transduction mechanism that might link magnetically-sensitive chemistry in CRY to an organism response.
Fogle et al. have shown that expression of DmCRY in central neurons in Drosophila is sufficient to bestow photosensitivity to those neurons, such that illumination with blue light (450–490 nm) increases action potential firing16. Thus, we hypothesise that a light-induced change to neuron activity levels, mediated by DmCRY, might be modified by external magnetic fields. To date no physical mechanism in a primary magnetoreceptor (CRY or magnetite) has been demonstrated to unequivocally produce a magnetically-induced response in neuronal activity17,18. As part of a study investigating the importance of patterned activity for the development of robust neural circuitry in the developing Drosophila embryonic CNS, we noted that exposing embryos to pulsed blue light (~470 nm) resulted in a heightened seizure-phenotype when tested post-embryonically at the third instar larval stage. Such a phenotype has been associated with, and is an indicator of, increased synaptic excitation in the locomotor circuitry19,20. We show in this study, that the effect of blue light pulses during embryogenesis is significantly potentiated by the presence of a magnetic field. The effect of both light and applied magnetic field is blocked by prior ingestion of typical antiepileptic drugs, indicative of a change to neuronal activity level. Moreover, the effect of both light and light + magnetic field requires the presence of DmCRY. Thus, we conclude that an applied magnetic field alters the ability of light-activated DmCRY to influence levels of synaptic excitation in the Drosophila CNS.
Results
To identify a magnetic field effect (MFE) on the CNS of Drosophila, we employed an established assay designed to probe how manipulation of neuronal activity during embryogenesis in Drosophila affects the probability of seizure in subsequent third instar larvae (~3 days later)19,20. Seizure duration is measured as the mean recovery time (MRT) of Drosophila larvae from a DC electric shock across the anterior-dorsal surface (approximating the position of the underlying CNS). Single gene mutations of the bang-sensitive (i.e. seizure-sensitive) grouping of Drosophila show a significantly extended MRT compared to wildtype. Electrophysiological analysis shows that this effect observed in larvae is associated with increased levels of synaptic excitation in the CNS of these mutants during embryogenesis19. Exposing wildtype embryos to pulsed blue light (470 nm, 100 ms on/900 ms off) during 11–19 h of embryogenesis (when the locomotor neural circuits form)21 results in subsequent larvae that show significantly increased seizure duration compared to control embryos that developed in constant darkness (using a 30 V/3 s electroshock, Figure 1a). We found this effect of light to be DmCRY-dependent; it is neither observed in a cry03 loss-of-function mutation (cry−/−), nor is it produced when using pulsed orange light of 590 nm peak wavelength (Figure 1a). It is known that light-activated DmCRY results in increased action potential firing in Drosophila arousal neurons16, which we hypothesise is sufficient to destabilise the development of the CNS leaving it prone to seizure19.
Significantly, repeating these experiments in the presence of a 100 mT magnetic field from a pair of NeFeB permanent magnets during the same period of embryogenesis substantially increased the effect of blue light on seizure severity in larvae compared to light-pulses alone (Figure 1a). We reproduced this MFE when a different researcher conducted equivalent experiments using a different population of flies, a different blue LED (from the same manufacturer) and a different electric shock stimulator (10 V/1.5 s). Qualitatively similar relative mean recovery times were recorded: control, 35.0 ± 7.2 s; blue light, 76.1 ± 13.3 s (P = 0.02 vs. control); blue light + magnetic field, 139.0 ± 15.5 s (P = 0.003 vs. control and blue light). The MFE on seizure duration was shown also to be DmCRY-dependent: being abolished in a cry03 null (cry−/−) background and rescued by transgenic expression of UAS-cry in a cry null (BL/MF/cry−/−/cry+, Figure 1a). Prolongation of seizure duration was also prevented by prior ingestion of typical antiepileptic drugs (e.g. phenytoin and gabapentin), consistent with an effect on neuronal activity (Figure 1a).
Although magnetic field exposure in the absence of light results in a marginally longer MRT than for the dark controls, the difference is not statistically significant (P > 0.99). Moreover, the MRT after exposure to a combination of blue light and magnetic field (137.3 ± 15.7 sec) is significantly longer than the MRT after exposure to blue light alone added to the MRT after exposure to magnetic fields alone (75.1 ± 9.1 sec, Figure 1b). The MFE is therefore dependent on light and is not simply an additive effect. The effect of antiepileptic drugs (phenytoin and gabapentin) is a strong indication that the increased seizure after exposure to blue light and magnetic field is related to increased synaptic excitation in the CNS. This result therefore represents an important initial step in unravelling the neuronal circuitry involved in CRY-dependent magnetoreception in Drosophila.
Discussion
We present a significant MFE on seizure duration in Drosophila larvae. These data were acquired using an established proxy measurement for perturbations to neuronal activity. A change in neuronal activity that results from the response of any primary magnetosensor is considered necessary to produce an organism response17,18. The effect we observe requires light and is DmCRY-dependent, the spin dynamics of which are potentially magnetically-sensitive via a photochemical radical pair mechanism3,4. Indeed, both low (<5 mT) and moderate (5–30 mT) magnetic fields have been reported to produce changes in quantum yield of flavin semiquinone radicals in photoreceptor CRY from Arabidopsis thaliana (AtCRY1)22.
By analogy, magnetically sensitive radical pair reaction dynamics in DmCRY may influence the concentration of FAD·−.There is evidence to suggest that this oxidation state of the flavin activates the protein in its role as circadian photoreceptor23. Conformational changes in the C-terminal tail of DmCRY, which is well placed to respond to the flavin oxidation state, were observed to be kinetically coupled to the single electron reduction (by light or chemically) of oxidised FAD to FAD·−. This conformational change appears to allow interaction with its partner protein, Timeless (TIM), which ultimately leads to degradation of TIM and resetting of the clock. Interestingly, DmCRY was found to revert back to its dark state conformation with the same kinetics as flavin reoxidation23. Consistent with this picture is the observation that clock neurons overexpressing DmCRY result in Drosophila with free-running circadian periods that show an enhanced response to a 300 µT applied MF8. However, the conserved triad of tryptophans thought to act as an electron transfer chain to the flavin to generate the photoinitiated radical pair are not necessary for DmCRY-dependent magnetic orientation of adult flies9. Moreover, light-induced conformational changes have also been observed in DmCRY where the flavin was reduced chemically to FAD·− prior to illumination24, and in variants containing tryp-triad mutations25. The authors of these studies argue that photoexcitation alone (of FAD·− or even oxidised FAD), without any subsequent electron transfer chemistry, might be sufficient to trigger activation of DmCRY24,25,26.
Alternatively, MFs might influence radical pair photochemistry in Drosophila via a mechanism that is independent of the CRY-TIM interaction that initiates signal transduction in the circadian clock. Light-activated DmCRY is also known to result in an increased firing rate of arousal neurons16. This pathway is a consequence of light initiated redox chemistry in DmCRY (which is likely to proceed via radical pair intermediates) that modulates potassium channels and results in membrane depolarisation. The fact that the MFE we observe is negated by prior ingestion of anti-epileptic drugs indicates the magnetically-sensitive activity of DmCRY is similarly impacting neuronal firing activity. However, whether our observations, or Drosophila magnetoreception in general, is dependent or independent of the flies' circadian clock is yet to be determined.
Exposing the embryos to a 100 mT magnetic field in the first instance has a range of benefits over the µT field exposures immediately relevant to animal magnetoreception. First, the radical pair mechanism predicts that fields of this magnitude will saturate the Zeeman effect of typical organic radical pairs14. This is likely to produce a magnetically-induced change in spin selective product yield and reaction kinetics that is larger than those expected from µT fields, and therefore might produce a larger physiological and organism response. Second, potential variations in background field are much less significant when using mT exposure conditions compared to µT conditions. Finally, the use of permanent magnets removes the confounding variables of vibration and heating that are possible when using the electromagnets necessary for µT exposure. These factors may have been significant in the history of conflicting reports in the context of biological MFEs from exposure to µT fields, which includes examples concerning the radical pair/CRY model of magnetoreception27,28. Moderate (mT) field exposure was therefore chosen as a rational and reliable starting point, which has provided us with greater confidence in the observed effect before µT exposure experiments are conducted.
Our results represent an important initial step in elucidating the signal transduction mechanism between the response of the putative primary magnetoreceptor, cryptochrome, and a behavioural response in a genetically tractable organism. This study paves the way for assessing the influence of the amplitude and orientation of Earth strength magnetic fields (~µT) on seizure duration in Drosophila larvae. Using similar methods to those employed by Fogle et al.16, we can also confirm whether the MFE observed here is mediated through light-dependent redox chemistry in DmCRY that is known to increase action potential firing in central brain neurones. This combined approach will provide a platform from which to detail the underlying electrophysiology of Drosophila magnetoreception.
Methods
Flies were maintained on standard corn meal medium at 25°C. Embryos were collected by allowing females to lay on grape-agar (Dutscher, Essex, UK) plates supplemented with a small amount of live yeast paste at 25°C. Flies used were Canton-S wildtype and cry03 homozygotes29. For rescue of DmCRY expression, the following stocks were crossed: ElaVC144-GAL4;;cry03 females crossed to UAS-Dmcry;cry01 males.
Magnetic field and light exposure during embryogenesis
Embryos (~100, 1–3 h after egg laying) were aligned in a central region (1 cm2) on a grape-agar plate in rows of 10 such that all had the same anterior-posterior orientation, which was aligned, where applicable, parallel to the magnet separation axis (Figure 2). The magnetic field within the 1 cm2 region containing the embryos was measured to be 100 ± 5 mT. The plate was placed in a humidified atmosphere inside a 25°C incubator and, where applicable, exposed to collimated light from an overhead LED (Cairn Research Ltd, UK, Figure 2). LEDs were used with peak emission at 470 nm (bandwidth 25 nm, irradiance 466 ± 14 nW cm−2) or 590 nm (bandwidth 18 nm, 1094 ± 18 nW cm−2). Embryos were exposed to light for 100 ms every second between 11–19 h after egg laying, but exposed to the magnetic field throughout embryogenesis. After hatching, larvae were transferred to vials and maintained in complete darkness and in the absence of any applied magnetic field until ~3 days later when wall climbing third instar larvae were tested for seizure-like behaviour.
Electroshock
Prior to stimulation, third instar larvae were washed to remove food residue and gently dried using paper tissue. Larvae were then allowed to recover on a plastic dish until normal crawling behaviour resumed. A stimulator, comprising two tungsten wires (0.1 mm diameter, ~1–2 mm apart) was placed across the anterior-dorsal surface, over the approximate position of the CNS. A DC pulse, generated by either a Grass S88 stimulator (30 V/3 s, Grass instruments, RI, USA) or constant current stimulator (10 V/1.5 s, DS2A, Digitimer, UK), was applied. The animal responded by tonically contracting and ceasing normal, motile behaviour. Time to resumption of normal motile behaviour was recorded (see [19] for more details). Results were analysed for significance using a one-way ANOVA with a Bonferroni post-hoc test.
Drug-feeding
Mated adult females were fed with phenytoin (0.4 mg per ml) or gabapentin (0.1 mg per ml) for 2 days by adding flies to food vials containing the drug. Drugs (Sigma, UK) were prepared in DMSO, which has no effect on MRT19. After this period, flies were transferred to laying pots and embryos collected. After magnetic field and/or light exposure, newly hatched larvae were placed into drug-free vials and third instars tested at the wall-climbing stage as described above.
Author Contributions
A.R.J. wrote the paper with N.S.S. and R.A.B. A.R.J. conceived and designed the method of magnetic field exposure during embryogenesis and R.A.B. and R.M. conceived and designed the light exposure conditions and electric shock assay. All experimental work was conducted by R.M and C.N.G.G. Data were analysed by R.M., C.N.G.G. and R.A.B. and results analysed by A.R.J., R.A.B. and N.S.S.
Acknowledgments
We are indebted to Dr. Ralf Stanewsky (UCL, UK) for providing flies. ARJ and NSS thank The University of Manchester, the Electromagnetic Fields Biological Research Trust, and the Colt Foundation for funding. RAB acknowledges support by the Wellcome Trust (090798/Z/09/Z) and MRC (MR/J009180/1). Work on this project benefited from the Manchester Fly Facility, established by The University of Manchester and the Wellcome Trust (087742). NSS is a Royal Society Wolfson Merit Award awardee and EPSRC Established Career Fellow.
References
- Kirschvink J. L. & Gould J. L. Biogenic magnetite as a basis for magnetic field detection in animals. Biosystems 13, 181–201 (1981). [DOI] [PubMed] [Google Scholar]
- Kirschvink J. L., Walker M. M. & Diebel C. E. Magnetite-based magnetoreception. Curr. Opin. Neurobiol. 11, 462–467 (2001). [DOI] [PubMed] [Google Scholar]
- Rodgers C. T. & Hore P. J. Chemical magnetoreception in birds: The radical pair mechanism. Proc. Natl. Acad. Sci. USA 106, 353–360 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dodson C. A., Hore P. J. & Wallace M. I. A radical sense of direction: signalling and mechanism in cryptochrome magnetoreception. Trends Biochem. Sci. 38, 435–446 (2013). [DOI] [PubMed] [Google Scholar]
- Wiltschko W. & Wiltschko R. Magnetic orientation and magnetoreception in birds and other animals. J. Comp. Physiol. A 191, 675–693 (2005). [DOI] [PubMed] [Google Scholar]
- Phillips J. B. & Sayeed O. Wavelength-dependent effects of light on magnetic compass orientation in Drosophila melanogaster. J. Comp. Physiol. A 172, 303–308, 10.1007/bf00216612 (1993). [DOI] [PubMed] [Google Scholar]
- Gegear R. J., Casselman A., Waddell S. & Reppert S. M. Cryptochrome mediates light-dependent magnetosensitivity in Drosophila. Nature 454, 1014–1018 (2008). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yoshii T., Ahmad M. & Helfrich-Förster C. Cryptochrome mediates light-dependent magnetosensitivity of Drosophila's circadian clock. PLoS Biol 7, e1000086 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gegear R. J., Foley L. E., Casselman A. & Reppert S. M. Animal cryptochromes mediate magnetoreception by an unconventional photochemical mechanism. Nature 463, 804–807 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Painter M. S., Dommer D. H., Altizer W. W., Muheim R. & Phillips J. B. Spontaneous magnetic orientation in larval Drosophila shares properties with learned magnetic compass responses in adult flies and mice. J Exp Biol 216, 1307–1316, 10.1242/jeb.077404 (2013). [DOI] [PubMed] [Google Scholar]
- Zoltowski B. D. et al. Structure of full-length Drosophila cryptochrome. Nature 480, 396–399 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levy C. et al. Updated structure of Drosophila cryptochrome. Nature 495, E3–E4 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Selby C. P. & Sancar A. The second chromophore in Drosophila photolyase/cryptochrome family photoreceptors. Biochemistry 51, 167–171 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steiner U. E. & Ulrich T. Magnetic field effects in chemical kinetics and related phenomena. Chem. Rev. 89, 51–147 (1989). [Google Scholar]
- Woodward J. R., Foster T. J., Jones A. R., Salaoru A. T. & Scrutton N. S. Time-resolved studies of radical pairs. Biochem. Soc. Trans. 37, 358–362 (2009). [DOI] [PubMed] [Google Scholar]
- Fogle K. J., Parson K. G., Dahm N. A. & Holmes T. C. CRYPTOCHROME Is a Blue-Light Sensor That Regulates Neuronal Firing Rate. Science 331, 1409–1413, 10.1126/science.1199702 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnsen S. & Lohmann K. J. The physics and neurobiology of magnetoreception. Nat Rev Neurosci 6, 703–712 (2005). [DOI] [PubMed] [Google Scholar]
- Lohmann K. J. Q. & A: Animal behaviour: Magnetic-field perception. Nature 464, 1140–1142 (2010). [DOI] [PubMed] [Google Scholar]
- Marley R. & Baines R. A. Increased persistent Na+ current contributes to seizure in the slamdance bang-sensitive Drosophila mutant. J Neurophysiol 106, 18–29, 10.1152/jn.00808.2010 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lin W.-H., Günay C., Marley R., Prinz A. A. & Baines R. A. Activity-Dependent Alternative Splicing Increases Persistent Sodium Current and Promotes Seizure. J. Neurosci. 32, 7267–7277 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Baines R. A. & Bate M. Electrophysiological Development of Central Neurons in theDrosophila Embryo. J Neurosci 18, 4673–4683 (1998). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maeda K. et al. Magnetically sensitive light-induced reactions in cryptochrome are consistent with its proposed role as a magnetoreceptor. Proc. Natl. Acad. Sci. USA 109, 4774–4779 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vaidya A. T. et al. Flavin reduction activates Drosophila cryptochrome. Proc. Natl. Acad. Sci. USA 110, 20455–20460 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozturk N., Selby C. P., Annayev Y., Zhong D. & Sancar A. Reaction mechanism of Drosophila cryptochrome. Proc. Natl. Acad. Sci. USA 108, 516–521 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozturk N., Selby C. P., Zhong D. & Sancar A. Mechanism of photosignaling by Drosophila cryptochrome: role of the redox status of the flavin chromophore. J. Biol. Chem. 289, 4634–4642 (2014). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ozturk N., Song S.-H., Selby C. P. & Sancar A. Animal type 1 cryptochromes: analysis of the redox state of the flavin cofactor by site-directed mutagenesis. J. Biol. Chem. 283, 3256–3263 (2008). [DOI] [PubMed] [Google Scholar]
- Ahmad M., Galland P., Ritz T., Wiltschko R. & Wiltschko W. Magnetic intensity affects cryptochrome-dependent responses in Arabidopsis thaliana. Planta 225, 615–624 (2007). [DOI] [PubMed] [Google Scholar]
- Harris S.-R. et al. Effect of magnetic fields on cryptochrome-dependent responses in Arabidopsis thaliana. J. R. Soc. Interface 6, 1193–1205 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dolezelova E., Dolezel D. & Hall J. C. Rhythm defects caused by newly engineered null mutations in Drosophila's cryptochrome Gene. Genetics 177, 329–345 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]