Heads of Laboratories
Richard E. Salomon Family Professor
Laboratory of Developmental Genetics
Research in the Shaham lab focuses on two areas: the control of programmed cell death during animal development and the roles of glial cells in nervous system development and function. The Shaham lab uses the roundworm Caenorhabditis elegans in its studies and has demonstrated that underlying both areas of research are cellular programs maintained through evolution from C. elegans to humans.
Nervous systems consist of two major cell types: neurons and glia. Basic properties of neurons and mechanisms governing neuronal development and function are well studied. However, the functions of glia, the most abundant cell type in vertebrate nervous systems, remain mostly unexplored, and few mediators of glial function are known. Glia are important in disease: 95 percent of brain malignancies are of glial character, and glial defects are associated with neurodegenerative diseases including amyotrophic lateral sclerosis and Alzheimer’s disease, suggesting that understanding glial functions, and how they go awry, is indispensable for comprehending brain functions and dysfunctions.
One explanation for the gap in understanding glia may lie in their neurotrophic properties. Glial manipulation often results in neuronal loss, precluding investigations of other effects glia may have on neuronal morphogenesis or activity. The Shaham lab has discovered that glia of the nematode C. elegans bear striking morphological, anatomical, and molecular similarities to vertebrate glia. Importantly, C. elegans glia are not required for neuronal survival, making C. elegans a unique model for deciphering glial roles in the nervous system and allowing, for the first time, manipulation of these cells in vivo without the complication of neuronal loss.
The Shaham lab has shown that glia are essential for neural development, promoting axon outgrowth and dendrite extension, and that glia are required for morphological plasticity of neuronal receptive endings; indeed, some sensory receptive structures fail to form in their absence. The lab has also uncovered morphology-independent roles for glia in sensory neuron function, showing that animals lacking glia exhibit profound sensory deficits. To understand the bases of these functional interactions, the Shaham lab has identified glia-enriched proteins and studied their roles in neuronal development and function.
Although C. elegans glia do not control neuronal survival, the Shaham lab has explored the death of other C. elegans cells to understand the principles by which vertebrate glia might control neuronal viability. In addition to discovering novel transcriptional and protein degradation-mediated controls of apoptotic cell death, the lab has identified a novel cell death program independent of known apoptotic regulators. The unique morphology accompanying this cell death program is conserved during development of the vertebrate nervous system. The Shaham lab identified many genes promoting this new cell death form, all of which are conserved in vertebrates, raising the possibility that the mechanism of this novel cell death program is also conserved.
A.B. in biochemistry and mathematics, 1989
Ph.D. in biology, 1995
Massachusetts Institute of Technology
University of California, San Francisco, 1996–2001
Assistant Professor, 2001–2007
Associate Professor, 2007–2012
The Rockefeller University
Sidney Kimmel Foundation for Cancer Research Scholar, 2002
Rita Allen Foundation Scholar, 2003
Irma T. Hirschl/Monique Weill-Caulier Trust Research Award, 2004
Masin Young Investigator Award, Breast Cancer Alliance, 2005
Klingenstein Fellowship, 2005
Blavatnik Award, 2009
Chiorazzi, M. et al. Related F-box proteins control cell death in Caenorhabditis elegans and human lymphoma. Proc. Natl. Acad. Sci. U.S.A. 110, 3943–3948 (2013).
Blum, E.S. et al. Control of nonapoptotic developmental cell death in Caenorhabditis elegans by a polyglutamine-repeat protein. Science 335, 970–973 (2012).
Oikonomou, G. et al. Opposing activities of LIT-1/NLK and DAF-6/patched-related direct sensory compartment morphogenesis in C. elegans. PLoS Biol. 9, e1001121 (2011).
Heiman, M.G. and Shaham, S. DEX-1 and DYF-7 establish sensory dendrite length by anchoring dendritic tips during cell migration. Cell 137, 344–355 (2009).
Bacaj, T. et al. Glia are essential for sensory organ function in C. elegans. Science 322, 744–747 (2008).