Lagenaur, Carl F.|
Associate Professor Emeritus, Neurobiology
Ph.D., University of Washington (1978)
Neurite outgrowth and synaptogenesis
Dr. Lagenaur's research interests centered on cell recognition events that are important in synapse formation and function. The laboratory studied two cell adhesion molecules, SIRP and CD47 which bind to one another and are localized to sites of synaptic contact. Both molecules have signaling capabilities and may be involved in regulation of synaptic plasticity. The goal of the laboratory's research was to determine how SIRP and CD47 signaling modify synaptic function. Work in collaboration with Drs. Cui and Weber, Dept. of Bioengineering, explored the use of neural cell adhesion molecules to improve bio-compatibility of chronic neural implants.
The surface immobilization of the neural adhesion molecule L1 on neural probes and its effect on neuronal density and gliosis at the probe/tissue interface.
Surface immobilization of neural adhesion molecule L1 for improving the biocompatibility of chronic neural probes: In vitro characterization.
Self-assembled monolayers of polythiophene conductive polymers improve biocompatibility and electrical impedance of neural electrodes.
Methylisothiazolinone, a neurotoxic biocide, disrupts the association of SRC family tyrosine kinases with focal adhesion kinase in developing cortical neurons.
Electrochemically controlled release of dexamethasone from conducting polymer polypyrrole coated electrode.
An L1-like molecule, the 8D9 antigen, is a potent substrate for neurite extension.
© Copyright 2001 - University
of Pittsburgh Department of Neurobiology