Fabrication of precisely aligned microwire and microchannel structures: Toward heat stimulation of guided neurites in neuronal cultures

2017 ◽  
Vol 214 (9) ◽  
pp. 1600729 ◽  
Author(s):  
Ka My Dang ◽  
Philipp Rinklin ◽  
Jan Schnitker ◽  
Bastian Haberkorn ◽  
Kathrin Zobel ◽  
...  
1989 ◽  
Vol 257 (4) ◽  
pp. C706-C713 ◽  
Author(s):  
L. M. Myers ◽  
C. Sumners

Previous studies determined that direct activation of protein kinase C (PKC) with phorbol esters increases the number of angiotensin II (ANG II)-specific binding sites in neuronal cultures prepared from the hypothalamus and brain stem of 1-day-old rats. In the physiological situation, PKC is activated by diacylglycerol, which can be produced by multiple pathways, such as stimulation of inositol phospholipid (IP) hydrolysis, phosphatidylcholine hydrolysis, or by de novo synthesis. In the present study we have examined whether stimulation of IP hydrolysis, and presumably activation of PKC, can mimic the actions of phorbol esters on ANG II-specific binding. We have incubated neuronal cultures with agents that increase IP hydrolysis and have determined the effects on ANG II-specific binding. Incubation of neuronal cultures with norepinephrine (NE) at concentrations (greater than 5 microM) and for times (15-60 min) that cause large increases in IP hydrolysis caused increases in the number of ANG II-specific binding sites, mimicking the actions of phorbol esters. The return of IP hydrolysis to control values was associated with a return of ANG II-specific binding to control levels. The upregulatory action of NE was abolished by prazosin, demonstrating the involvement of alpha 1-adrenergic receptors. In addition, this effect was blunted by the PKC antagonist H 7, suggesting PKC involvement in the response. Thus we have determined a potential physiological mechanism by which stimulation of IP hydrolysis by NE, and possible subsequent activation of PKC, leads to upregulation of ANG II-specific binding sites in neuronal cultures.(ABSTRACT TRUNCATED AT 250 WORDS)


2017 ◽  
Vol 890 ◽  
pp. 396-400 ◽  
Author(s):  
Zabihollah Tahery ◽  
Faraidoon Rahmanzai ◽  
Shigeyuki Date

To assure the quality and required workability of mortar or concrete, various types of superplasticizers are used. There are many factors affecting the performance of superplasticizers explicitly, type and dosage of the superplasticizers, type of cement, temperature and mixing procedure, as well as the addition times of the superplasticizers. Some researchers investigated the effect of delaying the addition time of superplasticizer to mortar or concrete, but there is not enough data about the effect of external temperature on performance of superplasticizers and consequent influences on fresh properties of mortar or concrete. In this research the effect of delaying the addition time of superplasticizers and influence of external temperature, namely, heat stimulation of superplasticizers, on fluidity, fresh density and air content of fresh cement mortar was investigated. Two types of Precast and Ready-Mix of Polycarboxylic acid-based ether superplasticizers with Ordinary Portland Cement was used. Delaying the addition time of superplasticizers enhanced the fluidity, slightly decreased the fresh density and increased the air content of mortar in comparison with simultaneous addition time with both heated and non-heated Superplasticizers.


2007 ◽  
Vol 6 (4) ◽  
pp. 744-752 ◽  
Author(s):  
Andrew W. Truman ◽  
Stefan H. Millson ◽  
James M. Nuttall ◽  
Mehdi Mollapour ◽  
Chrisostomos Prodromou ◽  
...  

ABSTRACT Yeast is rendered temperature sensitive with loss of the C-terminal (CT) domain of heat shock transcription factor (Hsf1). This domain loss was found to abrogate heat stimulation of Slt2 (Mpk1), the mitogen-activated protein kinase that directs the reinforced cell integrity gene expression needed for high-temperature growth. In Hsf1 CT domain-deficient cells, Slt2 still undergoes Mkk1/2-directed dual-Thr/Tyr phosphorylation in response to the heat stimulation of cell integrity pathway signaling, but the low Hsp90 expression level suppresses any corresponding increase in Slt2 kinase activity due to Slt2 being a “client” of the Hsp90 chaperone. A non-Hsf1-directed Hsp90 overexpression restored the heat induction of Slt2 activity in these cells, as well as both Slt2-dependent (Rlm1, Swi4) and Slt2-independent (MBF) transcriptional activities. Their high-temperature growth was also rescued, not just by this Hsp90 overexpression but by osmotic stabilization, by the expression of a Slt2-independent form of the Rlm1 transcriptional regulator of cell integrity genes, and by a multicopy SLT2 gene vector. In providing the elevated Hsp90 needed for an efficient activation of Slt2, heat activation of Hsf1 indirectly facilitates (Slt2-directed) heat activation of yet another transcription factor (Rlm1). This provides an explanation as to why, in earlier transcript analysis compared to chromatin immunoprecipitation studies, many more genes of yeast displayed an Hsf1-dependent transcriptional activation by heat than bound Hsf1 directly. The levels of Hsp90 expression affecting transcription factor regulation by Hsp90 client protein kinases also provides a mechanistic model for how heat shock factor can influence the expression of several non-hsp genes in higher organisms.


1999 ◽  
Vol 110 (8) ◽  
pp. 1475-1480 ◽  
Author(s):  
Massimiliano Valeriani ◽  
Domenico Restuccia ◽  
Vincenzo Di Lazzaro ◽  
Antonio Oliviero ◽  
Paolo Profice ◽  
...  

1964 ◽  
Vol 41 (3) ◽  
pp. 473-498
Author(s):  
P. MAKINGS

1. The term ‘Slifer's patches’ is applied in this paper to the series of specialized areas of cuticle which Slifer named ‘antennal crescents’ and ‘fenestrae’. None of the existing evidence supports her suggestion that these patches have a thermoreceptive function. Behaviour changes caused by damaging them can be reproduced by damaging other parts of the cuticle. The antennal-lowering response is not dependent upon stimulation of the patch situated near the antennal base. 2. Destruction of all of the patches does not reduce the ability of locusts to orientate to, and assume the basking posture under the influence of, a lamp; nor does it reduce their ability to respond similarly to a heat source in darkness and with a cooled floor on which the locusts move. It does not change the leaning response produced by heat stimulation of decapitated locusts. 3. The antennal scape and articular membrane are more effective in producing an antennal-lowering response when stimulated by a hot probe than are the antennal patches or adjacent areas. 4. The median response-time for kicking of the hind legs in response to the local application of a hot probe to the abdomen is shorter when the probe is applied to a part of the normal cuticle than when it is applied to a patch. 5. The antenna, including the flagellum, is sensitive to heat. Stimulation of the distal part of the flagellum by means of a hot wire produced an avoiding response when the wire temperature rose above 40° C. 6. If one antenna is removed locusts in arena tests show a marked tendency to turn the intact side of the body away from a lamp, or a heat source in darkness. Locusts with both antennae removed show a reduced tendency to akinesis under the influence of a heat source in darkness. 7. The detection by locusts of heat stimulation at intensities above the nociceptive threshold may depend on a sensory system which is at least partly distinct from that involved at lower intensities.


2007 ◽  
Vol 160 (1) ◽  
pp. 85-92 ◽  
Author(s):  
Carsten Dahl Mørch ◽  
Ole Kæseler Andersen ◽  
Thomas Graven-Nielsen ◽  
Lars Arendt-Nielsen

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