TY - JOUR
T1 - Differential cellular expression of neurotrophins in cortical tubers of the tuberous sclerosis complex
AU - Kyin, Robin
AU - Hua, Yue
AU - Baybis, Marianna
AU - Scheithauer, Bernd
AU - Kolson, Dennis
AU - Uhlmann, Erik
AU - Gutmann, David
AU - Crino, Peter B.
N1 - Funding Information:
This work was supported by funding from the Tuberous Sclerosis Alliance (to P. B. C. and D. H. G.) and the Center Without Walls, Parents Against Childhood Epilepsy, National Institute of Mental Health (grant K08–01658 ), and the Esther A. and Joseph Klingenstein Fund (P.B.C.).
PY - 2001/10
Y1 - 2001/10
N2 - Neurotrophins and their receptors modulate cerebral cortical development. Tubers in the tuberous sclerosis complex (TSC) are characterized histologically by disorganized cortical cytoarchitecture and thus, we hypothesized that expression of neurotrophin mRNAs and proteins might be altered in tubers. Using in situ transcription and mRNA amplification to probe cDNA arrays, we found that neurotrophin-3 (NT3) and trkB mRNA expression were reduced whereas neurotrophin-4 (NT4) and trkC mRNA expression were increased in whole tuber sections. Alterations in mRNA abundance were defined in single microdissected dysplastic neurons (DNs) and giant cells (GCs). NT3 mRNA expression was reduced in GCs and trkB mRNA expression was reduced in DNs. NT4 mRNA expression was increased in DNs and trkC mRNA expression was increased in both DNs and GCs. In three patients, TSC2 locus mutations were confirmed and the mean tuberin mRNA expression levels was reduced across all nine cases. Consistent with these observations, NT3 mRNA expression was reduced but trkC mRNA expression was increased in vitro in human NTera2 neurons (NT2N) transfected with a tuberin antisense construct that reduced tuberin expression. Western analysis of tuber homogenates and computer-assisted densitometry of immunolabeled sections confirmed the neurotrophin mRNA expression data in whole sections and single neurotrophin immunoreactive cells. We conclude that alterations in NT4/trkB and NT3/trkC expression may contribute to tuber formation during brain development as downstream effects of the hamartin and tuberinpathway in TSC.
AB - Neurotrophins and their receptors modulate cerebral cortical development. Tubers in the tuberous sclerosis complex (TSC) are characterized histologically by disorganized cortical cytoarchitecture and thus, we hypothesized that expression of neurotrophin mRNAs and proteins might be altered in tubers. Using in situ transcription and mRNA amplification to probe cDNA arrays, we found that neurotrophin-3 (NT3) and trkB mRNA expression were reduced whereas neurotrophin-4 (NT4) and trkC mRNA expression were increased in whole tuber sections. Alterations in mRNA abundance were defined in single microdissected dysplastic neurons (DNs) and giant cells (GCs). NT3 mRNA expression was reduced in GCs and trkB mRNA expression was reduced in DNs. NT4 mRNA expression was increased in DNs and trkC mRNA expression was increased in both DNs and GCs. In three patients, TSC2 locus mutations were confirmed and the mean tuberin mRNA expression levels was reduced across all nine cases. Consistent with these observations, NT3 mRNA expression was reduced but trkC mRNA expression was increased in vitro in human NTera2 neurons (NT2N) transfected with a tuberin antisense construct that reduced tuberin expression. Western analysis of tuber homogenates and computer-assisted densitometry of immunolabeled sections confirmed the neurotrophin mRNA expression data in whole sections and single neurotrophin immunoreactive cells. We conclude that alterations in NT4/trkB and NT3/trkC expression may contribute to tuber formation during brain development as downstream effects of the hamartin and tuberinpathway in TSC.
UR - http://www.scopus.com/inward/record.url?scp=0034794788&partnerID=8YFLogxK
U2 - 10.1016/S0002-9440(10)62539-4
DO - 10.1016/S0002-9440(10)62539-4
M3 - Article
C2 - 11583980
AN - SCOPUS:0034794788
SN - 0002-9440
VL - 159
SP - 1541
EP - 1554
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 4
ER -