Controlled epi-cortical delivery of epidermal growth factor for the stimulation of endogenous neural stem cell proliferation in stroke-injured brain

Abstract One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness. For the treatment of stroke, stimulation of endogenous neural stem/progenitor cells (NSPCs) by growth factors is a promising strategy for tis...

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Published inBiomaterials Vol. 32; no. 24; pp. 5688 - 5697
Main Authors Cooke, Michael J, Wang, Yuanfei, Morshead, Cindi M, Shoichet, Molly S
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.08.2011
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Abstract Abstract One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness. For the treatment of stroke, stimulation of endogenous neural stem/progenitor cells (NSPCs) by growth factors is a promising strategy for tissue regeneration. Epidermal growth factor (EGF) enhances proliferation of endogenous NSPCs in the subventricular zone (SVZ) when delivered directly to the ventricles of the brain; however, this strategy is highly invasive. We designed a biomaterials-based strategy to deliver molecules directly to the brain without tissue damage. EGF or poly(ethylene glycol)-modified EGF (PEG-EGF) was dispersed in a hyaluronan and methylcellulose (HAMC) hydrogel and placed epi-cortically on both uninjured and stroke-injured mouse brains. PEG-modification decreased the rate of EGF degradation by proteases, leading to a significant increase in protein accumulation at greater tissue depths than previously shown. Consequently, EGF and PEG-EGF increased NSPC proliferation in uninjured and stroke-injured brains; and in stroke-injured brains, PEG-EGF significantly increased NSPC stimulation. Our epi-cortical delivery system is a minimally-invasive method for local delivery to the brain, providing a new paradigm for local delivery to the brain.
AbstractList One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness. For the treatment of stroke, stimulation of endogenous neural stem/progenitor cells (NSPCs) by growth factors is a promising strategy for tissue regeneration. Epidermal growth factor (EGF) enhances proliferation of endogenous NSPCs in the subventricular zone (SVZ) when delivered directly to the ventricles of the brain; however, this strategy is highly invasive. We designed a biomaterials-based strategy to deliver molecules directly to the brain without tissue damage. EGF or poly(ethylene glycol)-modified EGF (PEG-EGF) was dispersed in a hyaluronan and methylcellulose (HAMC) hydrogel and placed epi-cortically on both uninjured and stroke-injured mouse brains. PEG-modification decreased the rate of EGF degradation by proteases, leading to a significant increase in protein accumulation at greater tissue depths than previously shown. Consequently, EGF and PEG-EGF increased NSPC proliferation in uninjured and stroke-injured brains; and in stroke-injured brains, PEG-EGF significantly increased NSPC stimulation. Our epi-cortical delivery system is a minimally-invasive method for local delivery to the brain, providing a new paradigm for local delivery to the brain.
Abstract One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness. For the treatment of stroke, stimulation of endogenous neural stem/progenitor cells (NSPCs) by growth factors is a promising strategy for tissue regeneration. Epidermal growth factor (EGF) enhances proliferation of endogenous NSPCs in the subventricular zone (SVZ) when delivered directly to the ventricles of the brain; however, this strategy is highly invasive. We designed a biomaterials-based strategy to deliver molecules directly to the brain without tissue damage. EGF or poly(ethylene glycol)-modified EGF (PEG-EGF) was dispersed in a hyaluronan and methylcellulose (HAMC) hydrogel and placed epi-cortically on both uninjured and stroke-injured mouse brains. PEG-modification decreased the rate of EGF degradation by proteases, leading to a significant increase in protein accumulation at greater tissue depths than previously shown. Consequently, EGF and PEG-EGF increased NSPC proliferation in uninjured and stroke-injured brains; and in stroke-injured brains, PEG-EGF significantly increased NSPC stimulation. Our epi-cortical delivery system is a minimally-invasive method for local delivery to the brain, providing a new paradigm for local delivery to the brain.
Author Cooke, Michael J
Morshead, Cindi M
Shoichet, Molly S
Wang, Yuanfei
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/21550655$$D View this record in MEDLINE/PubMed
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Issue 24
Keywords Stroke
Drug delivery
Epidermal growth factor
Tissue penetration
Hydrogel
Poly(ethylene glycol)
Language English
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  article-title: Enhanced neurogenesis following stroke
  publication-title: J Neurosci Res
  contributor:
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Snippet Abstract One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness....
One of the challenges in treating central nervous system (CNS) disorders with biomolecules is achieving local delivery while minimizing invasiveness. For the...
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SubjectTerms Advanced Basic Science
Animals
Brain - cytology
Brain - pathology
Cell Proliferation - drug effects
Dentistry
Drug delivery
Epidermal growth factor
Epidermal Growth Factor - chemistry
Epidermal Growth Factor - metabolism
Epidermal Growth Factor - therapeutic use
Hyaluronic Acid - chemistry
Hydrogel
Mice
Mice, Inbred BALB C
Models, Biological
Neural Stem Cells - cytology
Neural Stem Cells - metabolism
Peptide Hydrolases - metabolism
Poly(ethylene glycol)
Polyethylene Glycols - chemistry
Stroke
Stroke - drug therapy
Stroke - metabolism
Stroke - therapy
Tissue penetration
Title Controlled epi-cortical delivery of epidermal growth factor for the stimulation of endogenous neural stem cell proliferation in stroke-injured brain
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0142961211004273
https://dx.doi.org/10.1016/j.biomaterials.2011.04.032
https://www.ncbi.nlm.nih.gov/pubmed/21550655
https://search.proquest.com/docview/870551902
Volume 32
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