CV Science

nathalie Spassky PhD Developmental neurobiology

Course and current status

2010-present Group leader, Institut de Biologie de l’Ecole Normale Supérieure, Paris.

2003-2009 Independent Young Investigator. Hôpital Pitié Salpêtrière, Paris

Topic : Development and roles of ciliated cells during neurogenesis

2001-2002 Postdoctoral fellow. University of California San Francisco

Topic : Investigating the roles of the ependyma during adult neurogenesis

Advisor : Arturo Alvarez-Buylla

1996-2000 PhD. Hôpital Pitié Salpêtrière, Paris

Topic : Developmental origin of oligodendrocytes

Advisor : Bernard Zalc

Scientific summary

Our goal is to unravel the cellular and molecular mechanisms of neural stem cell biology. Neural stem cells are self-renewing multipotent progenitors, which can be used to replace neurons in degenerated or diseased nervous systems. However, many questions must be answered before neuronal replacement therapies using endogenous precursors become a reality. In particular, it is still unknown how the stem cell integrates the multiple signals from the environment that are responsible for its division, differentiation and survival. The existence of the primary cilium as a common feature of neural stem cells throughout life, and its location at the interface between the cytoplasm and the cerebral ventricle makes it a key organelle for the reception of such signals. Recent findings reveal that it is an antenna displaying specific receptors and relaying signals from these receptors to the cell body. Our goal is to understand the putative functions of the neural stem cell primary cilium during neurogenesis to provide new insights into the biology of neurogenesis and contribute to the development of new repair therapies.

We have shown that the neural stem cell primary cilium is crucial for proliferation in response to Sonic hed- gehog (Shh) during development in both the cerebellum and hippocampus. Joubert syndrome (JS) is an auto- somal recessive disorder characterized by a distinctive cerebellar malformation. Identified mutated genes related to this disease encode centrosomal or ciliary proteins, suggesting that JS is a ciliopathy. To identify precisely the molecular mechanisms leading to cerebellar malformation, we have undertaken a detailed analysis of human cerebellar development in JS fetuses and controls. To further identify the functions of neural stem cell pri- mary cilia in Shh-independent territories, we have generated conditional mutant mice in which cortical neu- roepithelial cells lack primary cilia from E9,5. Another line of research focuses on multiciliated ependymal cells lining the cerebral ventricles. Coordinated beating of their cilia is crucial to propel cerebrospinal fluid secreted by the choroid plexus. We have shown that these cells are derived from radial glial cells and that a coupling between hydro- dynamic forces and the planar cell polarity pathway is required to orient ciliary beating during development. Through interdisciplinary efforts with physics and medical groups in Paris, we aim to bridge the gap between intraventricular mechanisms and pathology and repair in neurodegenerative diseases.