Mental and other neurological disorders frequently surface during or near the end of development and, like the changes that occur in development, their symptoms are typically permanent. This provides strong evidence that developmental pathologies may be related to incidence of these disorders. In order to understand the effects of abnormalities in development, how they may give rise to symptoms of a mental or neurological disorder, and therefore what therapies might be appropriate, a baseline understanding of the principles that govern normal development is essential. Development is physically manifested in parts of the nervous system as a rewiring of synapses between classes of neurons and their targets. For the most part, the knowledge of the mechanisms that guide this process is poor. In easily accessible parts of the peripheral nervous system like the neuromuscular junction, techniques like in vivo fluorescence imaging and electrophysiology have revealed some information about the rewiring process that occurs there: in general, classes of neurons are initially highly interconnected and over development many of the connections are pruned, while surviving synapses are strengthened, resulting in a refined neural wiring. This process is called synapse elimination and is thought to be driven by synaptic activity and therefore experience. Similar techniques have been much less informative in the central nervous system, however. In order to overcome this barrier to understanding synaptic rewiring in higher learning centers, this project proposes to use serial section scanning electron microscopy to produce 3D volumes of high-resolution images of wild-type cerebellum tissue from mice in early postnatal development. Unlike other methods, the resolution of electron microscopy is sufficient to clearly identify all synapses in a tissue sample. Serial section scanning electron microscopy, a recent adaptation of this technique in which a long series of thin sections is cut, collected on tape, and automatically imaged, is capable of imaging blocks of tissue 100s of microns thick with minimal loss, and reasonably quickly. The cerebellum is a good system to investigate because it is intrinsically simple and compact. [In this project Purkinje cells and their climbing fiber inputs wll be reconstructed and the numbers, positions, and strengths of their synapses will be measured to establish a ground truth for this information. This will then be used to provide initial insight about the mechanisms underlying cerebellar rewiring by determining, first, whether this process is a minor refinement or a major rewiring; and second, whether or not the mediators of cerebellar rewiring are similar to those of peripheral synapse elimination. This work is an essential step toward understanding the underpinnings of normal development in the central nervous system, which will eventually lay the groundwork for investigations into the underlying causes of developmental disorders. A didactic neuroscience component is present in this training for the benefit of the investigator.]

Public Health Relevance

Many mental and neurological disorders have a time course that corresponds with development-for instance, patients with Tourette Syndrome begin to express symptoms in childhood, and the onset of schizophrenia typically occurs at the very beginning of adulthood-and once these symptoms present themselves very few therapies exist to reverse them (lifelong medication regimens often are required to alleviate symptoms). The coincidence of such disorders with development, a period during which a drastic and mostly permanent rearrangement of synapses in the nervous system occurs, constitutes strong evidence for the possibility that mental disorders are related to pathologies in the rewiring of synapses. In this research, I am proposing to use high-resolution imaging of volumes of normal brain tissue in mice, at several time points in early postnatal development, in order to better understand the morphological properties and underlying mechanisms that mediate normal synapse rewiring; the long-term goal of this work is to help establish a platform for comparison that can be used by studies aimed at understanding how abnormalities in this process give rise to symptoms of mental illness, and ways in which they may therefore be reversed.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31NS089223-02
Application #
8960827
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Gnadt, James W
Project Start
2014-12-01
Project End
2016-11-30
Budget Start
2015-12-01
Budget End
2016-11-30
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Harvard University
Department
Physics
Type
Schools of Arts and Sciences
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code