Heads of Laboratories
Ali H. Brivanlou, Ph.D.
Robert and Harriet Heilbrunn Professor
Laboratory of Stem Cell Biology and Molecular Embryology
The union of sperm and egg, two highly differentiated cell types, gives rise to the zygote — the totipotent cell. The zygote has the potential to form every cell type of the embryo and the adult organism through a series of hierarchical cell fate decisions that involves cell-cell interaction and signaling called embryonic induction. Dr. Brivanlou wants to decipher the molecular circuitry that underlies the establishment of discrete cell fate during early vertebrate embryogenesis.
The Brivanlou lab’s research focuses on the molecular events and cellular interactions that regulate the emergence of key structures in the early embryo. Most work in his laboratory focuses on the molecular basis of cell fate specification and patterning during early embryonic development. The ultimate objective is to understand the molecular circuitry underlying embryonic induction, with special emphasis on the formation of the nervous system. Toward this aim, he performs comparative studies using amphibian and mammalian model systems, including human embryonic stem cells (hESCs).
The Brivanlou laboratory has demonstrated that the TGF-β pathway plays a central role in inductive interactions leading to the establishment of different neural fates, which begins by the specification of the brain. Subsequent work in vertebrates has irrevocably established the pivotal role of these morphogens in the formation of specialized tissues in the embryo. In studies of frog (Xenopus laevis) embryos, Dr. Brivanlou has made several influential discoveries, including that all embryonic cells will develop into nerve cells unless they receive signals directing them otherwise. A concept, coined “the default model” of neural induction, postulates that neural fate determination requires the inhibition of an inhibitory signal. His laboratory has contributed to the molecular and biochemical understanding of the TGF-β signaling pathway and cross talk with other signaling networks, using frog and mouse embryos and mammalian cell culture. The work led to the discovery of the molecular basis of epidermal, neural crest and sensory placodes and neural induction in comparative platforms.
Information obtained from this work provides a strong foundation for research involving hESCs. To address whether the default model of neural induction is conserved from amphibians to mammals (and humans in particular), Dr. Brivanlou’s laboratory was among the first to work directly in hESCs. With private support from the Juvenile Diabetes Research Foundation, Dr. Brivanlou and colleagues derived several hESC lines, called RUES 1, 2 and 3. Using other private funds, his group established an in vivo platform to study hESCs by demonstrating these cells integrate into the mouse embryo, migrate to the inner cell mass when put in close contact and divide and differentiate alongside their mouse counterparts, suggesting the speed of differentiation of human cells can be reprogrammed to match the mouse. The RUES lines were among the first 13 hESC lines approved for use in research funded by the National Institutes of Health (NIH), under the NIH Guidelines for Human Stem Cell Research adopted in July 2009 under the Obama administration. In this context, the group has recently developed new tools to perform reversible transgenesis in human and rhesus monkey embryonic cell lines, expressing a variety of reporter constructs controlled by germ layer and tissue-specific regulatory elements. Their current work focuses on the molecular dissection of the defining properties of ESCs — their capacity for self-renewal and to differentiate into a range of cell types.
The Brivanlou laboratory’s overall goal is to use hESCs to study early human embryonic development. Several collaborations with Rockefeller University physics laboratories have also provided new insight, from the use of quantum dots for embryonic imaging (with Albert J. Libchaber) to development of new statistical tools for DNA microarray and high throughput proteomic analysis (with Marcelo O. Magnasco). An ongoing collaboration with Rockefeller’s Eric D. Siggia focuses on using a high throughput microfluidic platform, micropatterned control of colony architecture and optogenetic activation of gene expression to program hESC differentiation toward specific fates by dynamic changes of the signaling landscape and without compromising genetic integrity. Thus, the first steps of stem cell differentiation are being scrutinized using new high-resolution techniques. This data will be organized and developed into a predictive tool to rationally reprogram specialized fates from hESCs.
Dr. Brivanlou received his doctoral degree in 1990 from the University of California, Berkeley, and his postdoctoral training in Douglas Melton’s lab at Harvard University. He joined Rockefeller in 1994 as assistant professor. Among his many awards are the Irma T. Hirschl/Monique Weill-Caulier Trusts Career Scientist Award, the Searle Scholar Award, the James A. Shannon Director’s Award from the NIH, the Presidential Early Career Award for Scientists and Engineers and The Rockefeller University Teaching Award.
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