eye graphic
Schepens Home Page
Description
Program of Study
Eligibility and Application
Faculty and Affiliates
Program Trainees
Calendar of Seminars
Useful Links

Jessica Pisano, Ph.D.

Department of Molecular and Cellular Biology
Harvard University
16 Divinity Ave.
Cambridge, MA 02138
Tel.: (617) 495-2599

E-Mail: jpisano@fas.harvard.edu

Sponsor
John Dowling, Ph.D.

dowling@fas.harvard.edu

 

"As I am new to the field of vision sciences, being selected for this training grant was an honor. It has proven to be a rare chance to get introduced both to the field (via the eye course) and to some of the top researchers in the field. It is giving me a real leg-up in terms of my career in the cell biology of vision."

PAST: A complex organism begins with a small number of cells that have the potential to give rise to all the cell types represented in the mature organism. As development proceeds there is a simultaneous increase in cell number and specialization of cell type. Thus, restriction, the inability to alter ones identity in response to a set of environmental signals, must occur during development and lineage divergence. It was my goal to define the molecular mechanisms and cellular changes that are responsible for cell fate restriction. I defined a developmental stage when lineage restriction occurs in rat enteric and sympathetic neural precursors. In order to identify the critical molecular events responsible for restriction, it is necessary to understand the cellular changes that take place during enteric and sympathetic neuronal development. I have examined the effects of purified biological molecules implicated in peripheral neuronal development and complex profiles of environmental signals on isolated neural precursors. Together, these studies help us to understand the molecules and developmental programs that direct lineage divergence, neuronal maturation and phenotypic restriction in the peripheral nervous system.  

PRESENT:  The archie mutation increases retinal ganglion cell death; archie mutant zebrafish die before the full impact of this mutation can be defined. Eye transplantation will provide information about what types of ganglion cells are affected in the archie mutant and how this depletion impacts on development and wiring of the retina.

Publications

Pisano, J.M. and Birren, S.J. (1999) Restriction of developmental potential during divergence of the enteric and sympathetic neuronal lineages. Development 126:2855-2868.

Lockhart, S.T., Mead, J.M., Pisano, J.M., Slonimsky, J.D. and Birren, S.J. (2000) Nerve growth factor collaborates with myocyte derived factors to promote development of presynaptic sites in cultured sympathetic neurons. J. Neuro. Bio. 42: 460-476.

Worley, D.W., Pisano, J.M*., Choi, E.D., Walus, L., Hession, C.A., Cate, R.L., Sanicola, M. and Birren, S.J. (2000) Developmental regulation of GDNF response and receptor expression in the enteric nervous system. Development 127: 4383-4393.

Pisano, J.M., Colon, F. and Birren, S.J. (2000) Post-migratory enteric and sympathetic neural precursors share common, developmentally regulated, responses to BMP2. Dev. Bio. 227: 1-11.


Comments to: vision_training@vision.eri.harvard.edu
Last updated: November 8, 2002