HDAC inhibition amplifies gap junction communication in neural progenitors: potential for cell-mediated enzyme prodrug therapy.
Exp Cell Res
; 313(13): 2958-67, 2007 Aug 01.
Article
in En
| MEDLINE
| ID: mdl-17555745
ABSTRACT
Enzyme prodrug therapy using neural progenitor cells (NPCs) as delivery vehicles has been applied in animal models of gliomas and relies on gap junction communication (GJC) between delivery and target cells. This study investigated the effects of histone deacetylase (HDAC) inhibitors on GJC for the purpose of facilitating transfer of therapeutic molecules from recombinant NPCs. We studied a novel immortalized midbrain cell line, NGC-407 of embryonic human origin having neural precursor characteristics, as a potential delivery vehicle. The expression of gap junction protein connexin 43 (Cx43) was analyzed by western blot and immunocytochemistry. While Cx43 levels were decreased in untreated differentiating NGC-407 cells, the HDAC inhibitor 4-phenylbutyrate (4-PB) increased Cx43 expression along with increased membranous deposition in both proliferating and differentiating cells. Simultaneously, Ser 279/282-phosphorylated form of Cx43 was declined in both culture conditions by 4-PB. The 4-PB effect in NGC-407 cells was verified by using HNSC.100 human neural progenitors and Trichostatin A. Improved functional GJC is of imperative importance for therapeutic strategies involving intercellular transport of low molecular-weight compounds. We show here an enhancement by 4-PB, of the functional GJC among NGC-407 cells, as well as between NGC-407 and human glioma cells, as indicated by increased fluorescent dye transfer.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Prodrugs
/
Drug Delivery Systems
/
Gap Junctions
/
Stem Cell Transplantation
/
Enzyme Inhibitors
/
Histone Deacetylase Inhibitors
/
Neurons
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Exp Cell Res
Year:
2007
Document type:
Article
Affiliation country:
Sweden