The information below refers to time of the award.
Silvia Arber was born in 1968 in Geneva and studied biology at the Biozentrum of the University of Basel. She graduated in 1995 with a doctorate in the laboratory of Pico Caroni at the Friedrich Miescher Institute for Biomedical Research (FMI) in Basel. After a postdoctoral fellowship in the laboratory of Thomas Jessell at Columbia University in New York, she returned to Basel in 2000 to establish her independent research group on neuronal circuits controlling motor behavior. She holds a joint appointment as a Professor of Neurobiology at the Biozentrum and a Senior group leader at the FMI in Basel.
Silvia Arber was elected as a member of the European Molecular Biology Organization (EMBO) in 2005. She is also a member of the Swiss Academy of Medical Sciences, the American Association for the Advancement of Science and the Academia Europaea. She has been recognized for her outstanding research with numerous prizes, including the Pfizer Research Prize (1998), the National Latsis Prize (2003), the Friedrich Miescher Award (2008), and the Otto Naegeli Prize (2014).
Animals carry out an enormous repertoire of distinct actions, spanning from seemingly simple repetitive tasks like walking to more complex movements requiring fine motor skills. The central nervous system, composed of the brain and spinal cord, integrates information received from the body and coordinates its activity. Within the central nervous system, neurons never function in isolation, they are organised into neuronal circuits which are at the core of choosing, maintaining, adjusting and terminating distinct motor behaviours to coordinate movement.
Over the last decade, Silvia Arber’s laboratory has demonstrated that neuronal circuits are organized into precise modules by functional subdivision at multiple levels of the motor system, including the spinal cord and the brainstem. Thus, precisely connected neuronal subpopulations in the motor system align with the distinct behavioural functions, allowing for functional subdivision of labour and diversification of motor programs. Silvia Arber’s work provides important insight into the mechanisms and organizational principles responsible for the establishment and function of the motor system. She has decisively contributed to a better understanding of how neuronal circuits control and orchestrate movement.
Shorten and reproduced with permission from EMBO Molecular Medicine. Arber S (2017) “Organization and function of neuronal circuits controlling movement”. EMBO Mol Med doi:10.15252/emmm.201607226.
Movement is essential for survival and represents the final behavioral output of many computations in the nervous system. One of the most striking characteristics associated with movement is the seemingly endless repertoire of distinct actions and motor programs that our bodies can generate, raising the important question of the underlying neuronal circuit mechanisms that are at the core of regulating different forms of movement. Motor control relevant parameters can be measured throughout the nervous system, indicating that information about movement is broadly distributed. This feature is also underscored by the fact that many diseases affecting the nervous system lead to perturbation in movement, often severely disabling affected patients.
To understand how the various sensory systems functionally assemble and process incoming information, it has been very fruitful in the past to study the organization of neuronal circuits at their first steps into the nervous system. This collective work has unraveled the high precision with which information is processed as well as the identity of involved neuronal subpopulations and their functions. In contrast, much less was known about whether and how motor output pathways at the opposite end of the nervous system follow an organizational logic at the level of neuronal circuits, and how such a circuit logic might translate into different functions in the regulation of movement. This commentary summarizes some of the work my laboratory has contributed recently to the understanding of circuit-level organizational principles within the final output pathways of the motor system, and how this anatomical work relates to functional parameters in the execution of movement.
Motor neurons in the spinal cord are spatially organized into motor neuron pools, each innervating a distinct skeletal muscle in the periphery. Since body movement is a result of coordinated muscle contractions, it is essential to understand how different motor neuron pools are recruited in line with the biomechanical ability of the innervated muscles, a property largely determined by the identity of synaptic inputs to these motor neurons. An important question was therefore whether studying the distribution and identity of neuronal populations premotor (i.e. with direct synaptic connections to motor neurons) to functionally distinct groups of motor neurons could be leveraged to visualize and understand the organization of functionally distinct connectivity matrices in the spinal cord. Such approaches were made possible by recent technological advances on genetically modified versions of rabies viruses for transsynaptic tracing, restricting their labeling potential to directly connected (monosynaptic) neuronal populations.
We applied this emerging technology to reveal the spatial distribution of spinal premotor neurons connected to motor neuron pools of different function (Stepien et al., 2010). In this first study, we found that premotor interneurons distribute over many segments of the spinal cord, and that patterns are highly reproducible across individuals, but distinct for different motor neuron pools. After this proof-of-principle study, we asked whether distinct premotor populations regulate motor neurons responsible to control stance (extension) and swing (flexion) phases in the locomotor sequence (Tripodi et al., 2011). We found that in the overall neuronal distribution pattern, extensor premotor interneurons in the spinal cord are located more medially than their flexor counterparts (Figure 1A), illustrating the existence of an anatomical trace correlating with motor function even at a circuit level only one step away from actual execution. Moreover, the basis for these spatial and connectivity differences is laid down during development, when postmitotic neurons giving rise to extensor and flexor premotor neurons are generated from the same progenitor domain territory but at different developmental time points (Figure 1A; Tripodi et al., 2011). In more recent work, we demonstrated that interneurons premotor to motor neurons regulating postural muscles involved in trunk stability, and with very distinct function from limb muscles, show a bilaterally symmetrical distribution in the spinal cord, while counterparts associated with the control of limb muscles are biased towards the ipsilateral spinal cord (Goetz et al., 2015). We also found that alternation of axon guidance molecules on genetically defined interneurons downstream of transcription factors can alter premotor connectivity patterns and lead to behavioral abnormalities (Satoh et al., 2016). Lastly, the majority of studies on spinal interneurons in the past and in particular the ones linking developmental transcriptional identity to locomotor function focused mostly on local interneuron circuitry (Arber, 2012). In recent work, we describe the diverse genetic identity, synaptic organization and function of spinal neurons with long axonal projections (Ruder et al., 2016). We found that cervical neurons with long descending projections to the lumbar spinal cord subdivide into genetically tractable neuronal subpopulations with distinct connections, in part based on developmental origin (Figure 1B), and that the overall neuronal population plays an important role in the regulation of whole-body locomotor parameters to ensure stability of locomotion, including regulation of postural stability and speed-dependent interlimb coordination (Ruder et al., 2016). In summary, our work on the organization of motor circuits in the spinal cord reveals that understanding precise connectivity patterns and genetic identities can provide important insight into functional circuit properties in the motor output system within the spinal cord. They raise the question of whether similar principles might apply to descending pathways from the brain, a line of studies we have recently carried out and that is described in the next section.
While the spinal cord is clearly an essential component for the execution of body movements, it is well established that it cannot generate movement without external input. The most striking demonstration of this point is the observation that patients with complete spinal cord injuries exhibit paralysis of body parts regulated by spinal segments below injury. External input sources to the spinal cord include most importantly descending pathways from the brain and sensory feedback from the periphery. This commentary will solely focus on communication between supraspinal centers in the brainstem and the spinal cord, and in particular address the organization of connectivity in relation to behavioral function.
Species with four limbs including humans make extensive use of their extremities, but rostral and caudal extremities show important functional differences, and these are conserved across evolution. The most striking difference is the use of forelimbs for precise manipulation tasks, a functional property almost lacking for hindlimbs in most species. Our experimental approaches to understand whether there are anatomical correlates to these behavioral differences was to uncover sites in the brain in which neurons reside with direct connections to spinal motor neurons innervating forelimb or hindlimb muscles, using transsynaptic rabies virus tracing experiments with monosynaptic restriction (Esposito et al., 2014; Figure 2A). Strikingly, we identified more brainstem subregions with neurons establishing direct connections to forelimb than hindlimb innervating motor neurons (Figure 2A). In particular, there were three regions that showed almost exclusively connections to fore- but not hindlimb innervating motor neurons, named MdV, PCRt and SpV (Esposito et al., 2014). Moreover, we identified three regions with indiscriminate connectivity profiles to both kinds of motor neurons and these neurons were found in a bilaterally distributed pattern (Mc, Pn, Gi). And lastly, two brainstem regions showed higher connectivity to hindlimb innervating motor neuron populations compared forelimb counterparts (Ve, SpVe).
To follow up on these anatomy-based connectivity findings, we started to dissect how subpopulations of brainstem neurons are embedded in motor output pathways and what their functions in the regulation of motor behavior are. We found that within the caudally located MdV brainstem nucleus, only glutamatergic neurons establish synaptic connections to very specific forelimb-muscle innervating motor neuron pools. In functional studies, we revealed that these excitatory MdV neurons do not have a role in regulating locomotion, but that in the functional absence of these neurons either by specific ablation or by transient pharmacogenetic silencing approaches, mice were significantly impaired in carrying out a forelimb-reaching and retrieval task for single food pellets. Most notably, we traced the defect specifically to the grasping phase of the unilateral forelimb behavior (Figure 2A), and no deficiency was found in the reaching phase towards the food pellet or the retrieval phase back to the mouth (Esposito et al., 2014). A second topic we studied is the connectivity from the vestibular nucleus to hindlimb-innervating motor neurons (Basaldella et al., 2015). As previously found in cats, these synaptic inputs are directed preferentially to extensor over flexor hindlimb innervating motor neurons also in mice, but within extensor motor neuron pools, synaptic inputs are targeted in high number to slow- over fast type motor neurons (Figure 2B). Since this motor neuron subclass is recruited for postural tasks, the revealed specific connectivity matrix from brainstem vestibular neurons thus matches perfectly this behavioral requirement. We found that the precision of these synaptic connections is established during development and requires multisensory signaling from both vestibular and proprioceptive sources (Basaldella et al., 2015). A third example of a functionally dedicated pathway was described in a recent collaborative study, in which we identified specific neurons in the periaqueductal gray in the midbrain involved in the regulation of defensive behavior, signaling through the caudal brainstem nucleus Mc (Tovote et al., 2016). Finally, ascending communication from the spinal cord to supraspinal centers is also essential for accurate motor behavior. In this context, we have recently identified a complex connectivity matrix between spinal neurons and the brainstem nucleus LRN, composed of distinct genetically identifiable subpopulations with specific connectivity patterns (Figure 2C; Pivetta et al., 2014).
In summary, current evidence from our work and recent studies by other investigators that cannot be described here due to space limitations, begin to suggest that the identification of functionally dedicated subpopulations in the brainstem, defined by position, genetic identity and connectivity, is instrumental to understand the function of these neurons in the regulation of motor behavior. The emerging theme is that these subpopulations and their associated circuitry represent dedicated modules that are at the core of regulating diverse motor actions and programs. Future work will reveal how many of these modules exist, how they interact with each other, and how circuits involved in competing motor programs decide on actual behavior to be carried out.
The theme that anatomical connectivity patterns prefigure behavioral function can be used as entry point to gain a deeper understanding of the neuronal circuits underlying the regulation of motor behavior, and in particular action diversification. It will be important to understand how motor centers in the brainstem interact with final executive circuits in the spinal cord to implement motor programs for body control, and how higher motor centers involved in decision making and action sequence generation interact with neuronal circuits in the brainstem. In the long run, understanding the healthy configuration of these circuits and how they function will likely be very useful for developing strategies to interfere with movement disorders, often affecting higher motor centers, but for which considerable amelioration might be achieved by interference at a level of neuronal circuits closer to execution, including the spinal cord and the brainstem. From our own recent work, we found that a specific source of sensory feedback derived from muscle spindles is absolutely essential to drive functional recovery after incomplete spinal cord injury (Takeoka et al., 2014). Notably, the observed functional recovery processes were paralleled by circuit reorganization in the spinal cord establishing detour circuits across the lesion site, and these circuit adjustments were also impaired in the absence of muscle spindle feedback. Together, these findings suggest that not only for the healthy nervous system, but also in disease or after injury, it is crucial to understand the response properties of specific neuronal subpopulations to gain access to key circuit mechanisms to interfere with nervous system dysfunction. I am convinced that future discoveries in this direction will drive the process of developing medicines for the impaired nervous system.
Motor circuit organization in the spinal cord
Motor modules in the brainstem
Arber, S. (2012). Neuron 74, 975-89.
Basaldella, E., Takeoka, A., Sigrist, M., and Arber, S. (2015). Cell 163, 301-12.
Esposito, M.S., Capelli, P., and Arber, S. (2014). Nature 508, 351-6.
Goetz, C., Pivetta, C., and Arber, S. (2015). Neuron 85, 131-44.
Pivetta, C., Esposito, M.S., Sigrist, M., and Arber, S. (2014). Cell 156, 537-48.
Ruder, L., Takeoka, A., and Arber, S. (2016). Neuron, Nov 16, ePub ahead of print.
Satoh, D., Pudenz, C., and Arber, S. (2016). Neuron 89, 1046-58.
Stepien, A.E., Tripodi, M., and Arber, S. (2010). Neuron 68, 456-72.
Tovote, P., et al. (2016). Nature 534, 206-12.
Tripodi, M., Stepien, A.E., and Arber, S. (2011). Nature 479, 61-6.
Takeoka, A., Vollenweider, I., Courtine, G., and Arber, S. (2014). Cell 159, 1626-39.
University of Basel
Department of Cell Biology
Telephone: +41 61 207 20 57 (office)
Telephone: +41 61 207 20 58/64 (lab)
Friedrich Miescher Institute