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1 CNTF and neurturin expression in the cochlear nucleus wa
2 CNTF binds to high or low affinity receptor complexes co
3 CNTF immunoreactivity was observed on astrocytes and oli
4 CNTF increased STAT3 phosphorylation in WT and SOCS3kd m
5 CNTF increases rapidly and greatly following traumatic o
6 CNTF induced an extensive activation of astrocytes, whic
7 CNTF induces a decrease in rhodopsin expression and an i
8 CNTF reduced diabetes incidence and islet apoptosis in W
9 CNTF treatment resulted in a dose-dependent increase in
10 CNTF viral transduction maintained rhodopsin expression
11 CNTF was identified in a subset of type B cells that lab
12 CNTF was increased and also expressed by neurons.
13 CNTF, anti-CNTF antibodies, and antibodies to the encaps
14 CNTF-/- mice had more extensive tissue loss and similar
15 CNTF-receptor complex members, CNTFRalpha, LIFRbeta and
16 CNTF/LIF/STAT3 signaling has been shown to promote their
21 d motor neurons, indicating that these adult CNTF receptors play no essential survival role in this m
24 ression in the OC of deafened rats, although CNTF was expressed throughout the time that SGNs were dy
26 were quantified (by Western blot analysis), CNTF stimulation leading to the upregulation of connexin
27 enic response is indirect; that is, NT-3 and CNTF first bind to nascent neurons in the DRG--which the
31 xon regeneration, Muller cell activation and CNTF production in the retina without affecting retinal
32 (NT-3), BDNF, GDNF, neurturin, artemin, and CNTF-in the OC and cochlear nucleus at various ages from
36 ons of BDNF, CNTF, a combination of BDNF and CNTF, or PEDF in one eye and PBS in the other 2 days bef
37 hic factor (CNTF), a combination of BDNF and CNTF, or pigment epithelial cell-derived growth factor (
38 eurotrophic factor receptor (CNTFRalpha) and CNTF (0.83 nM) responsiveness in connexin 43 upregulatio
39 ctor receptor alpha subunit (CNTFRalpha) and CNTF play important roles in neuron survival, glial diff
41 By quantitative PCR, interleukin-6, LIF, and CNTF mRNA increased but with significantly different tim
43 adenomatus polyposis coli (APC(+)) OLs, and CNTF significantly increased the percentage of APC(+) OL
44 endogenous neuroprotective system (TRPV1 and CNTF on astrocytes, and CNTFRalpha on dopamine neurons)
46 these patients were evaluated for CNTF, anti-CNTF antibodies, and antibodies to the encapsulated cell
49 demonstrate that aspirin-induced astroglial CNTF was also functionally active and that supernatants
51 ts received intravitreal injections of BDNF, CNTF, a combination of BDNF and CNTF, or PEDF in one eye
57 0 in rods also demolishes neuroprotection by CNTF and prevents further activation of Muller glia.
62 TAT3, a transcription factor up-regulated by CNTF and to a lesser extent FGF-2, was also detected.
63 y assigned to receive s.c. recombinant CNTF (CNTF(Ax15); 0.1 mg x kg(-1) per day; n = 11) calorie-res
65 /Interleukin-6/IL-6Ralpha hexameric complex, CNTF/CNTF-Ralpha heterodimerizes gp130 and LIF-R via non
72 and wounded corneas, resulting in decreased CNTF and impaired sensory nerve innervation and regenera
76 ted viral vectors (type 2) containing either CNTF, BDNF, or both, with saline-injected eyes and nonin
77 amine the in vivo roles played by endogenous CNTF receptors in adult motor neuron survival and ChAT m
80 ion with our previous study, that endogenous CNTF receptor signaling can protect MNs against toxic in
81 Together, the data suggest that endogenous CNTF receptor signaling in type B stem cells inhibits ad
83 TF receptor alpha (CNTFRalpha), an essential CNTF receptor component, is greatly increased in skeleta
84 d reinnervation in normal corneas, exogenous CNTF accelerated nerve regeneration in the wounded corne
85 elucidate a cellular mechanism for exogenous CNTF-triggered neuroprotection and provide insight into
86 ding diseases, the target cells of exogenous CNTF and its mechanism of action remain poorly understoo
90 treatment of previously preserved explants, CNTF responsiveness was 174% +/- 23% (P = 0.023; 4 pairs
92 ombined treatment with OPC grafts expressing CNTF can enhance remyelination and facilitate functional
93 ant adeno-associated virus (rAAV) expressing CNTF was injected subretinally, for transduction of peri
97 oop, increasing ciliary neurotrophic factor (CNTF) and basic fibroblast growth factor (bFGF) producti
98 re, we examined ciliary neurotrophic factor (CNTF) and fibroblast growth factor-2 (FGF-2) expression,
99 uent release of ciliary neurotrophic factor (CNTF) and leukaemia inhibitory factor (LIF) potently pro
100 anisms by which ciliary neurotrophic factor (CNTF) and other neurotrophic molecules modify the axonal
101 y, we evaluated ciliary neurotrophic factor (CNTF) delivered via an intraocular encapsulated cell tec
107 n, the cytokine ciliary neurotrophic factor (CNTF) induces hypophagia and increases signal transducti
108 of the cytokine ciliary neurotrophic factor (CNTF) into the rat striatum, in the absence of neurodege
113 ting induced by ciliary neurotrophic factor (CNTF) is qualitatively different from the sprouting indu
120 that endogenous ciliary neurotrophic factor (CNTF) receptor signaling may inhibit neuronal differenti
121 reatment with a ciliary neurotrophic factor (CNTF) small-molecule peptide mimetic, Peptide 021 (P021)
122 ty trial, human ciliary neurotrophic factor (CNTF) was delivered by cells transfected with the human
123 upregulation of ciliary neurotrophic factor (CNTF) was observed within the retina following optic ner
125 termine whether ciliary neurotrophic factor (CNTF), a combination of BDNF and CNTF, or pigment epithe
126 h factor (HGF), ciliary neurotrophic factor (CNTF), and Artemin through specific activation of their
129 factor 1 (IGF1)/ciliary neurotrophic factor (CNTF), induces regrowth of retinal axons and formation o
130 gs treated with ciliary neurotrophic factor (CNTF), to examine the effect of a neuroprotective stimul
132 s production of ciliary neurotrophic factor (CNTF), which prevents the active degeneration of dopamin
137 ce to DA fouling of a carbon nanotube fiber (CNTF) microelectrode to a traditional carbon fiber (CF)
139 signaling in SVZ NSP cells, with a "floxed" CNTF receptor alpha (CNTFRalpha) mouse line and a gene c
140 mples from these patients were evaluated for CNTF, anti-CNTF antibodies, and antibodies to the encaps
142 viable cells with minimal cell loss and gave CNTF output at levels previously shown to be therapeutic
146 Intravitreal injection of recombinant human CNTF protein in rat results in a series of biochemical a
147 entivirus to deliver the same secreted human CNTF used in clinical trials to a mouse model of RP.
148 elivered by cells transfected with the human CNTF gene and sequestered within capsules that were surg
150 ogenesis was reduced by approximately 20% in CNTF-/- mice, confirming the endogenous role of CNTF.
151 lost endogenous membrane-bound CNTFRalpha in CNTF signaling, suggesting the potential of an adjuvant
154 n blot, there was a quantitative increase in CNTF and BDNF expression in retinas exposed to single vi
156 type mice by approximately 25-75% but not in CNTF-/- littermates or in the SVZ of mice infused with C
158 ervation did not affect SVZ proliferation in CNTF-/- mice, suggesting that the dopaminergic innervati
159 % more per year in sham-treated eyes than in CNTF-treated eyes (P < 0.001, linear mixed model), and c
162 retinal layers were significantly thicker in CNTF-treated eyes than in sham-treated eyes (P < 0.005).
163 ischemia does not seem to directly increase CNTF, as intrastriatal injection of an ischemic solution
164 ent with the D2 agonist quinpirole increased CNTF mRNA in the SVZ and hippocampal formation, and in c
166 vates astrocytes and Muller cells, increases CNTF levels in the retina and leads to enhanced retinal
167 ine-aspartic acid) blocking peptides induced CNTF expression, which was dependent on transcription.
170 romoted by suppression of CASP2 and CASP6 is CNTF-dependent and mediated through the JAK/STAT signall
172 ), showed a significant binding in the lenti-CNTF-injected striatum that was saturated and displaced
174 role in progenitor survival and maturation, CNTF acts as a chemoattractant and participates in the r
175 pports hindlimb motor neurons through c-Met; CNTF supports subsets of axial motor neurons through CNT
180 at, although neither motor neuron nor muscle CNTF receptors play a significant, nonredundant role in
181 e most abundant in the postnatal hearing OC; CNTF and neurturin most abundant in the cochlear nucleus
184 show first that subcutaneous application of CNTF to levator auris longus muscles of adult mice evoke
186 VZ) cells in vivo with low concentrations of CNTF to anatomically characterize cells containing funct
191 re urgently needed to evaluate the effect of CNTF treatment in patients with inherited retinal degene
193 an intracellular mediator of the effects of CNTF and other neurotrophic cytokines, acts locally in a
194 abrogation of aspirin-induced expression of CNTF by siRNA knockdown of CREB, the presence of a conse
196 lial activation, increases the expression of CNTF in culture, and subsequently increases the number o
197 rin increased mRNA and protein expression of CNTF in primary mouse and human astrocytes in a dose- an
198 n previously that constitutive expression of CNTF prevents photoreceptor death but alters the retinal
199 ohistochemistry to analyze the expression of CNTF receptor alpha (CNTFRalpha) in mouse retina and opt
214 olecule, Bcl2, known down stream products of CNTF signalling were also increased in MS cortical neuro
216 sus cAMP-response element in the promoter of CNTF, and the recruitment of CREB and CREB-binding prote
223 enhanced green fluorescent protein (EGFP) or CNTF and transplanted into the contused adult thoracic s
225 to the anorectic action of either leptin or CNTF(Ax15), implying a crucial role for S6K1 in modulati
226 were used as vehicle versus CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated (24 hours, 37 d
229 opic analysis of the full-length gp130/LIF-R/CNTF-Ralpha/CNTF quaternary complex elucidates an asymme
230 s of the full-length gp130/LIF-R/CNTF-Ralpha/CNTF quaternary complex elucidates an asymmetric structu
233 cipated in a phase 2 clinical trial received CNTF delivered by an encapsulated cell technology implan
237 andomly assigned to receive s.c. recombinant CNTF (CNTF(Ax15); 0.1 mg x kg(-1) per day; n = 11) calor
238 paminergic denervation in adult mice reduced CNTF mRNA by approximately 60%, whereas systemic treatme
240 e receptor gp130 gene in Muller glia reduces CNTF-dependent photoreceptor survival and prevents phosp
242 en neurons and astrocytes normally represses CNTF expression and that neuronal dysfunction causes a r
243 RNA levels in CNTF-treated and (rhCNTFRalpha+CNTF)-treated paired corneas averaged (mean+/-SEM) 0.26+
244 s CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated (24 hours, 37 degrees C), followed by anal
248 deo time-lapse imaging), we demonstrate that CNTF controls the directed migration of SVZ-derived prog
253 ied using Western blots, which revealed that CNTF protein continually rose through 28 days post injur
255 n acute model of demyelination, we show that CNTF is strongly re-expressed after lesion and is involv
263 us limiting its high-frequency behavior, the CNTF shows a significantly higher durability than the CF
264 us neuregulin activity completely blocks the CNTF-induced proliferation and reduces about half of the
265 on of 100 muM DA, the signal measured by the CNTF microelectrode shows a 2-h window over which no dec
267 w that the CNTF-binding alpha-subunit of the CNTF receptor (CNTFRalpha) is released from injured tiss
268 nd adult-onset conditional disruption of the CNTF receptor alpha (CNTFRalpha) gene to directly examin
269 ibody targeted to the gp130 component of the CNTF receptor) and AG490 (an inhibitor of the JAK/STAT p
271 rating retina, whereas studies show that the CNTF-binding alpha-subunit of the CNTF receptor (CNTFRal
272 ment of CREB and CREB-binding protein to the CNTF promoter by aspirin suggest that aspirin increases
273 tural features with CNTF and signals via the CNTF receptor tripartite complex comprised of CNTFRalpha
276 ns and leads to behavioural recovery through CNTF receptor alpha (CNTFRalpha) on nigral dopamine neur
277 y nerve innervation and regeneration through CNTF and that diabetes reduces DC populations in UW and
280 scue from cell death, continuous exposure to CNTF changed photoreceptor cell profiles, especially res
281 lpha from axons renders RGCs unresponsive to CNTF, thereby contributing to regenerative failure and d
284 an donor corneas were used as vehicle versus CNTF-treated or CNTF- versus (rhCNTFRalpha+CNTF)-treated
288 to different patterns of initiation: whereas CNTF-induced sprouts emerge randomly from the surface of
292 trophic factor, and the mechanisms by which CNTF expression could be increased in the brain are poor
296 ares functional and structural features with CNTF and signals via the CNTF receptor tripartite comple
298 elivered by ECT implants was 51 months, with CNTF levels statistically equivalent between the 6- and
299 oved retinal function 1 week after PDT, with CNTF and the combination of BDNF and CNTF reducing mfERG
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