|
|
||||||||
továDepartment of Physiology and Neuroscience, New York University School of Medicine, New York, New York 10016
Submitted 6 April 2004; accepted in final form 19 July 2004
Epidermal growth factor (EGF) stimulates proliferation, process outgrowth, and survival in the CNS. Understanding the actions of EGF necessitates characterizing its distribution in brain tissue following drug delivery or release from cellular sources. We used the integrative optical imaging (IOI) method to measure diffusion of fluorescently labeled EGF (6,600 Mr; 4 µg/ml) in the presence of excess unlabeled EGF (90 µg/ml) to compete off specific receptor binding and reveal the "true" EGF diffusion coefficient following injection in rat brain slices (400 µm). The effective diffusion coefficient was 5.18 ± 0.16 x 107 (SE) cm2/s (n = 22) in rat somatosensory cortex and the free diffusion coefficient, determined in dilute agarose gel, was 16.6 ± 0.12 x 107 cm2/s (n = 27). Tortuosity (
), a parameter representing the hindrance imposed on EGF by the convoluted brain extracellular space (ECS), was 1.8, the lowest yet measured by IOI for a protein in brain. Control experiments with fluorescent dextran of similar molecular weight and tetramethylammonium confirmed EGF did not affect local ECS structure. We conclude that transport of smaller growth factors such as EGF through brain ECS is less hindered than that of larger proteins (>10,000 Mr, e.g., nerve growth factor) where typically
> 2.1. Modeling was used to predict that low
will allow EGF sources in the brain to be further from target cells and still elicit a biological response. High
values for larger growth factors imply more constrained local biological effects than with smaller proteins such as EGF.
This article has been cited by other articles:
![]() |
R. G. Thorne, A. Lakkaraju, E. Rodriguez-Boulan, and C. Nicholson In vivo diffusion of lactoferrin in brain extracellular space is regulated by interactions with heparan sulfate PNAS, June 17, 2008; 105(24): 8416 - 8421. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y. Guy, M. Sandberg, and S. G. Weber Determination of {zeta}-Potential in Rat Organotypic Hippocampal Cultures Biophys. J., June 1, 2008; 94(11): 4561 - 4569. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. V. Nauman, P. G. Campbell, F. Lanni, and J. L. Anderson Diffusion of Insulin-Like Growth Factor-I and Ribonuclease through Fibrin Gels Biophys. J., June 15, 2007; 92(12): 4444 - 4450. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. G. Thorne and C. Nicholson In vivo diffusion analysis with quantum dots and dextrans predicts the width of brain extracellular space PNAS, April 4, 2006; 103(14): 5567 - 5572. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Kay and K. Toth Influence of Location of a Fluorescent Zinc Probe in Brain Slices on Its Response to Synaptic Activation J Neurophysiol, March 1, 2006; 95(3): 1949 - 1956. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Yoshioka, R. N. Prince, H. Huang, S. B. Perkins, F. U. Cruz, C. MacGillivray, D. A. Lauffenburger, and R. T. Lee Cardiomyocyte hypertrophy and degradation of connexin43 through spatially restricted autocrine/paracrine heparin-binding EGF PNAS, July 26, 2005; 102(30): 10622 - 10627. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |