TY - JOUR
T1 - Coexpression of neurotrophic growth factors and their receptors in human facial motor neurons
AU - Li, Jing Min
AU - Brackmann, Derald E.
AU - Linthicum, Fred H.
AU - Hitselberger, William E.
AU - Lim, David J.
PY - 1999/1/1
Y1 - 1999/1/1
N2 - Neuronal development and maintenance of facial motor neurons is believed to be regulated by neurotrophic growth factors. Using celloidin-embedded sections, we evaluated immunoreactivity of 11 neurotrophic factors and their receptors in facial nuclei of human brain stems (4 normal cases, and 1 from a patient with facial palsy and synkinesis). In the normal subjects, positive immunoreactivity of the growth factor neurotrophin-4 and acidic fibroblast growth factor (aFGF) was observed in facial motor neurons, as was positive immunoreactivity against ret, the receptor shared by glial cell line-derived neurotrophic factor and neurturin. Immunoreactivity was moderate for the receptor trkB and strong for trkC. In the case of partial facial palsy, surviving cells failed to show immunoreactivity against neurotrophins. However, immunoreactivity of aFGF was up-regulated in both neuronal and non- neuronal cells in this patient. Results suggest that these trophic growth factors and their receptors may protect facial neurons from secondary degeneration and promote regrowth of the facial nerve after axotomy or injury.
AB - Neuronal development and maintenance of facial motor neurons is believed to be regulated by neurotrophic growth factors. Using celloidin-embedded sections, we evaluated immunoreactivity of 11 neurotrophic factors and their receptors in facial nuclei of human brain stems (4 normal cases, and 1 from a patient with facial palsy and synkinesis). In the normal subjects, positive immunoreactivity of the growth factor neurotrophin-4 and acidic fibroblast growth factor (aFGF) was observed in facial motor neurons, as was positive immunoreactivity against ret, the receptor shared by glial cell line-derived neurotrophic factor and neurturin. Immunoreactivity was moderate for the receptor trkB and strong for trkC. In the case of partial facial palsy, surviving cells failed to show immunoreactivity against neurotrophins. However, immunoreactivity of aFGF was up-regulated in both neuronal and non- neuronal cells in this patient. Results suggest that these trophic growth factors and their receptors may protect facial neurons from secondary degeneration and promote regrowth of the facial nerve after axotomy or injury.
KW - Facial motor neurons
KW - Neurotrophic factors
KW - Receptors
UR - http://www.scopus.com/inward/record.url?scp=0345425105&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0345425105&partnerID=8YFLogxK
U2 - 10.1177/000348949910800915
DO - 10.1177/000348949910800915
M3 - Article
C2 - 10527284
AN - SCOPUS:0345425105
SN - 0003-4894
VL - 108
SP - 903
EP - 908
JO - Annals of Otology, Rhinology and Laryngology
JF - Annals of Otology, Rhinology and Laryngology
IS - 9 I
ER -