scholarly journals Temporal Modulation of a GPCR Pathway Elucidates Band-Pass Processing for the Downstream Signaling and Transcription Factor Activation

2016 ◽  
Vol 110 (3) ◽  
pp. 143a
Author(s):  
Madhuresh Sumit ◽  
Richard R. Neubig ◽  
Shuichi Takayama ◽  
Jennifer J. Linderman
2015 ◽  
Vol 7 (11) ◽  
pp. 1378-1386 ◽  
Author(s):  
M. Sumit ◽  
R. R. Neubig ◽  
S. Takayama ◽  
J. J. Linderman

Pulsatile stimulation of a GPCR pathway reveals that the downstream signal activation is optimized for intermediate frequencies in a band-pass manner that can be explained by the kinetics of the signaling pathway.


Pneumologie ◽  
2012 ◽  
Vol 66 (11) ◽  
Author(s):  
K Hoehne ◽  
H Eibel ◽  
M Grimm ◽  
M Idzko ◽  
J Müller-Quernheim ◽  
...  

2021 ◽  
Vol 25 ◽  
pp. 233121652097802
Author(s):  
Emmanuel Ponsot ◽  
Léo Varnet ◽  
Nicolas Wallaert ◽  
Elza Daoud ◽  
Shihab A. Shamma ◽  
...  

Spectrotemporal modulations (STM) are essential features of speech signals that make them intelligible. While their encoding has been widely investigated in neurophysiology, we still lack a full understanding of how STMs are processed at the behavioral level and how cochlear hearing loss impacts this processing. Here, we introduce a novel methodological framework based on psychophysical reverse correlation deployed in the modulation space to characterize the mechanisms underlying STM detection in noise. We derive perceptual filters for young normal-hearing and older hearing-impaired individuals performing a detection task of an elementary target STM (a given product of temporal and spectral modulations) embedded in other masking STMs. Analyzed with computational tools, our data show that both groups rely on a comparable linear (band-pass)–nonlinear processing cascade, which can be well accounted for by a temporal modulation filter bank model combined with cross-correlation against the target representation. Our results also suggest that the modulation mistuning observed for the hearing-impaired group results primarily from broader cochlear filters. Yet, we find idiosyncratic behaviors that cannot be captured by cochlear tuning alone, highlighting the need to consider variability originating from additional mechanisms. Overall, this integrated experimental-computational approach offers a principled way to assess suprathreshold processing distortions in each individual and could thus be used to further investigate interindividual differences in speech intelligibility.


Immunity ◽  
2008 ◽  
Vol 29 (5) ◽  
pp. 704-719 ◽  
Author(s):  
Stéphane Bécart ◽  
Ann J. Canonigo Balancio ◽  
Céline Charvet ◽  
Sonia Feau ◽  
Caitlin E. Sedwick ◽  
...  

2020 ◽  
Author(s):  
Emmanuel Ponsot ◽  
Léo Varnet ◽  
Nicolas Wallaert ◽  
Elza Daoud ◽  
Shihab A. Shamma ◽  
...  

AbstractSpectrotemporal modulations (STMs) offer a unified framework to probe suprathreshold auditory processing. Here, we introduce a novel methodological framework based on psychophysical reverse-correlation deployed in the modulation space to characterize how STMs are detected by the auditory system and how cochlear hearing loss impacts this processing. Our results show that young normal-hearing (NH) and older hearing-impaired (HI) individuals rely on a comparable non-linear processing architecture involving non-directional band-pass modulation filtering. We demonstrate that a temporal-modulation filter-bank model can capture the strategy of the NH group and that a broader tuning of cochlear filters is sufficient to explain the overall shift toward temporal modulations of the HI group. Yet, idiosyncratic behaviors exposed within each group highlight the contribution and the need to consider additional mechanisms. This integrated experimental-computational approach offers a principled way to assess supra-threshold auditory processing distortions of each individual.


2002 ◽  
Vol 159 (5) ◽  
pp. 867-880 ◽  
Author(s):  
Lisette Hari ◽  
Véronique Brault ◽  
Maurice Kléber ◽  
Hye-Youn Lee ◽  
Fabian Ille ◽  
...  

β-Catenin plays a pivotal role in cadherin-mediated cell adhesion. Moreover, it is a downstream signaling component of Wnt that controls multiple developmental processes such as cell proliferation, apoptosis, and fate decisions. To study the role of β-catenin in neural crest development, we used the Cre/loxP system to ablate β-catenin specifically in neural crest stem cells. Although several neural crest–derived structures develop normally, mutant animals lack melanocytes and dorsal root ganglia (DRG). In vivo and in vitro analyses revealed that mutant neural crest cells emigrate but fail to generate an early wave of sensory neurogenesis that is normally marked by the transcription factor neurogenin (ngn) 2. This indicates a role of β-catenin in premigratory or early migratory neural crest and points to heterogeneity of neural crest cells at the earliest stages of crest development. In addition, migratory neural crest cells lateral to the neural tube do not aggregate to form DRG and are unable to produce a later wave of sensory neurogenesis usually marked by the transcription factor ngn1. We propose that the requirement of β-catenin for the specification of melanocytes and sensory neuronal lineages reflects roles of β-catenin both in Wnt signaling and in mediating cell–cell interactions.


1995 ◽  
Vol 766 (1 Receptor Acti) ◽  
pp. 245-252 ◽  
Author(s):  
STEFFEN JUNG ◽  
AVRAHAM YARON ◽  
IRIT ALKALAY ◽  
ADA HATZUBAI ◽  
AYELET AVRAHAM ◽  
...  

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