STUDIES OF GAUCHER DISEASE AND OTHER NEUROGENETIC DISORDERS

影响神经系统的人类遗传疾病的临床研究

The clinical study of human genetic disorders affecting the nervous system is important for the successful development of diagnostic techniques and strategies for therapy. This goal is also facilitated by a comprehensive knowledge of the biochemistry and clinical heterogeneity of the disorder. Gaucher disease, the most common sphingolipidosis, is extremely useful as a model because of the occurrence of both neuronopathic and non-neuronopathic phenotypes, as well as the broad spectrum of clinical diversity within the major types of the disorder, can be studied. Once the pathophysiologic mechanisms of systemic involvement in this enzyme deficiency disorder are understood, the therapy of nervous system dysfunction may be more rationally approached. Basic research on glucocerebrosidase, the enzyme deficient in Gaucher disease, has generated a more detailed understanding of the structure, biosynthesis, intracellular routing, and turnover of the enzyme. These studies will complement other studies within our branch focusing on the investigation of the potential and efficacy of gene transfer as a therapeutic approach. Targeted homologous recombination in embryonic stem cells is used to develop appropriate transgenic animal models of Gaucher disease and other genetic disorders affecting the nervous system. Recombinant production of human enzymes and activator proteins is directed toward the development of effective enzyme and gene replacement strategies.