Ciba foundation symposium 160: Regeneration of vertebrate sensory receptor cells

1992 ◽  
Vol 111 (2) ◽  
pp. 236
Author(s):  
Brian M. Davis
2000 ◽  
Vol 201 (6) ◽  
pp. 467-473 ◽  
Author(s):  
M. Matsuoka ◽  
Junko Yoshida-Matsuoka ◽  
Richard M. Costanzo ◽  
Masumi Ichikawa

2006 ◽  
Vol 6 ◽  
pp. 1841-1850 ◽  
Author(s):  
Francoise Mazet

The vertebrate cranial sensory placodes are ectodermal embryonic patches that give rise to sensory receptor cells of the peripheral paired sense organs and to neurons in the cranial sensory ganglia. Their differentiation and the genetic pathways that underlay their development are now well understood. Their evolutionary history, however, has remained obscure. Recent molecular work, performed on close relatives of the vertebrates, demonstrated that some sensory placodes (namely the adenohypophysis, the olfactory, and accoustico-lateralis placodes) first evolved at the base of the chordate lineage, while others might be specific to vertebrates. Combined with morphological and cellular fate data, these results also suggest that the sensory placodes of the ancestor of all chordates differentiated into a wide range of structures, most likely to fit the lifestyle and environment of each species.


Neuron ◽  
2011 ◽  
Vol 71 (3) ◽  
pp. 389-405 ◽  
Author(s):  
Olivia Bermingham-McDonogh ◽  
Thomas A. Reh

1996 ◽  
Vol 76 (2) ◽  
pp. 1340-1343 ◽  
Author(s):  
G. Gomez ◽  
J. Atema

1. Adaptation and disadaptation rates determine the temporal response properties of sensory receptor cells. In chemoreception, temporal filter properties of receptor cells are poorly understood. We studied the time course of disadaptation in lobster antennular chemoreceptor cells by using in situ high-resolution stimulus measurement and extracellularly recorded spike responses. Fifteen receptor cells were each tested with two series (one at 10 microM, one at 100 microM) of three odor (hydroxyproline) pulses: a 200-ms test pulse, a 5-s adapting pulse, and a 200-ms probe pulse after time intervals ranging from 1 to 60 s. After complete adaptation by the adapting pulse, individual cells recovered at different rates. After 1 s, a third of the cells responded with a mean response of 3 spikes/cell, representing approximately 20% recovery. All cells fully recovered between 10 and 30 s. Mean full recovery was within 25 s, with a time constant of 14 s, independent of stimulus concentration.


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