Neutralizing Antibodies to proNGF and proBDNF Provide
Neuroprotection. (A) Mice were infused intranasally with
anti-proNGF, anti-proBDNF, or control IgG immediately
after the CCI. At 3 days of recovery, sections were
stained for NeuN and counterstained with DAPI to reveal
the area of damage. (B) The area of total damage comprised
of the area of tissue loss and the penumbra (dotted line),
where the density of DAPI and NeuN staining was reduced.
The percentage of the total area of damage (relative to
the contralateral hemisphere) was significantly reduced by
the antiproneurotrophin antibodies. Scale bar = 200 µm.
(C) Representative images of TUNEL staining in the
penumbra showed fewer apoptotic cells in the mice that
received anti-proNGF or anti-proBDNF. Scale bar = 50 µm.
Data were collected from 3 to 4 animals per group. Graphs
depict the means ± SEM. Asterisks indicate significance by
one-way analysis of variance followed by Tukey’s post hoc
analysis with p < .05.
IgG = immunoglobulin G; proBDNF = pro-brain-derived
neurotrophic factor; proNGF = pro-nerve growth factor;
DAPI = 4′,6′-diamidino-2-phenylindole; TUNEL = terminal
deoxynucleotidyl transferase deoxyuridine triphosphate
nick end labeling.