Striola magica. A functional explanation of otolith geometry

Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvatu...

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Vydáno v:	Journal of computational neuroscience Ročník 35; číslo 2; s. 125 - 154
Hlavní autoři:	Dimiccoli, Mariella, Girard, Benoît, Berthoz, Alain, Bennequin, Daniel
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Boston Springer US 01.10.2013 Springer Nature B.V Springer Verlag
Témata:	Acceleration Algorithms Animals Biomedical and Life Sciences Biomedicine Biophysics Cognitive science Computer Simulation Hair Cells, Auditory, Inner - physiology Hair Cells, Auditory, Inner - ultrastructure Human Genetics Models, Neurological Neural Pathways - physiology Neurology Neurons, Afferent - physiology Neuroscience Neurosciences Otolithic Membrane - cytology Otolithic Membrane - physiology Otolithic Membrane - ultrastructure Rats Saccule and Utricle - physiology Sensation - physiology Theory of Computation Vestibule, Labyrinth - physiology Otolith organs Striola Vestibular pathway
ISSN:	0929-5313, 1573-6873, 1573-6873
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Abstract	Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvature and torsion. It has been shown that the striolar region is functionally different from the rest, being involved in a phasic vestibular pathway. We propose a mathematical and computational model that explains the necessity of this amazing geometry for the striola to be able to carry out its function. Our hypothesis, related to the biophysics of the hair cells and to the physiology of their afferent neurons, is that striolar afferents collect information from several type I hair cells to detect the jerk in a large domain of acceleration directions. This predicts a mean number of two calyces for afferent neurons, as measured in rodents. The domain of acceleration directions sensed by our striolar model is compatible with the experimental results obtained on monkeys considering all afferents. Therefore, the main result of our study is that phasic and tonic vestibular afferents cover the same geometrical fields, but at different dynamical and frequency domains.
AbstractList	Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvature and torsion. It has been shown that the striolar region is functionally different from the rest, being involved in a phasic vestibular pathway. We propose a mathematical and computational model that explains the necessity of this amazing geometry for the striola to be able to carry out its function. Our hypothesis, related to the biophysics of the hair cells and to the physiology of their afferent neurons, is that striolar afferents collect information from several type I hair cells to detect the jerk in a large domain of acceleration directions. This predicts a mean number of two calyces for afferent neurons, as measured in rodents. The domain of acceleration directions sensed by our striolar model is compatible with the experimental results obtained on monkeys considering all afferents. Therefore, the main result of our study is that phasic and tonic vestibular afferents cover the same geometrical fields, but at different dynamical and frequency domains. Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvature and torsion. It has been shown that the striolar region is functionally different from the rest, being involved in a phasic vestibular pathway. We propose a mathematical and computational model that explains the necessity of this amazing geometry for the striola to be able to carry out its function. Our hypothesis, related to the biophysics of the hair cells and to the physiology of their afferent neurons, is that striolar afferents collect information from several type I hair cells to detect the jerk in a large domain of acceleration directions. This predicts a mean number of two calyces for afferent neurons, as measured in rodents. The domain of acceleration directions sensed by our striolar model is compatible with the experimental results obtained on monkeys considering all afferents. Therefore, the main result of our study is that phasic and tonic vestibular afferents cover the same geometrical fields, but at different dynamical and frequency domains.Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvature and torsion. It has been shown that the striolar region is functionally different from the rest, being involved in a phasic vestibular pathway. We propose a mathematical and computational model that explains the necessity of this amazing geometry for the striola to be able to carry out its function. Our hypothesis, related to the biophysics of the hair cells and to the physiology of their afferent neurons, is that striolar afferents collect information from several type I hair cells to detect the jerk in a large domain of acceleration directions. This predicts a mean number of two calyces for afferent neurons, as measured in rodents. The domain of acceleration directions sensed by our striolar model is compatible with the experimental results obtained on monkeys considering all afferents. Therefore, the main result of our study is that phasic and tonic vestibular afferents cover the same geometrical fields, but at different dynamical and frequency domains. Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction. In mammals, the striola, parallel to the line where hair cells reverse their polarization, is a narrow region centered on a curve with curvature and torsion. It has been shown that the striolar region is functionally different from the rest, being involved in a phasic vestibular pathway. We propose a mathematical and computational model that explains the necessity of this amazing geometry for the striola to be able to carry out its function. Our hypothesis, related to the biophysics of the hair cells and to the physiology of their afferent neurons, is that striolar afferents collect information from several type I hair cells to detect the jerk in a large domain of acceleration directions. This predicts a mean number of two calyces for afferent neurons, as measured in rodents. The domain of acceleration directions sensed by our striolar model is compatible with the experimental results obtained on monkeys considering all afferents. Therefore, the main result of our study is that phasic and tonic vestibular afferents cover the same geometrical fields, but at different dynamical and frequency domains.[PUBLICATION ABSTRACT]
Author	Girard, Benoît Berthoz, Alain Bennequin, Daniel Dimiccoli, Mariella
Author_xml	– sequence: 1 givenname: Mariella surname: Dimiccoli fullname: Dimiccoli, Mariella email: mariella.dimiccoli@math-info.univ-paris5.fr organization: Laboratoire de Mathématiques Appliquées à Paris 5 (MAP5), Université Paris Descartes (Paris V) – sequence: 2 givenname: Benoît surname: Girard fullname: Girard, Benoît organization: Institut des Systèmes Intelligents et de Robotique (ISIR), Université Pierre et Marie Curie (Paris VI), CNRS Institut des Systèmes Intelligents et de Robotique (ISIR) – sequence: 3 givenname: Alain surname: Berthoz fullname: Berthoz, Alain organization: Laboratoire de Physiologie de la Perception et de l’Action (LPPA), Collège-de-France – sequence: 4 givenname: Daniel surname: Bennequin fullname: Bennequin, Daniel organization: Géométrie et dynamique, Université Paris Diderot (Paris VII)
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Keywords	Otolith organs Striola Vestibular pathway
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Snippet	Otolith end organs of vertebrates sense linear accelerations of the head and gravitation. The hair cells on their epithelia are responsible for transduction....
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SubjectTerms	Acceleration Algorithms Animals Biomedical and Life Sciences Biomedicine Biophysics Cognitive science Computer Simulation Hair Cells, Auditory, Inner - physiology Hair Cells, Auditory, Inner - ultrastructure Human Genetics Models, Neurological Neural Pathways - physiology Neurology Neurons, Afferent - physiology Neuroscience Neurosciences Otolithic Membrane - cytology Otolithic Membrane - physiology Otolithic Membrane - ultrastructure Rats Saccule and Utricle - physiology Sensation - physiology Theory of Computation Vestibule, Labyrinth - physiology
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Title	Striola magica. A functional explanation of otolith geometry
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