Synaptophysin is a selective marker for axons in human cutaneous end organ complexes.


Journal

Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft
ISSN: 1618-0402
Titre abrégé: Ann Anat
Pays: Germany
ID NLM: 100963897

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 10 01 2022
revised: 04 04 2022
accepted: 24 04 2022
pubmed: 20 5 2022
medline: 22 6 2022
entrez: 19 5 2022
Statut: ppublish

Résumé

Small clear synaptic-like vesicles fill axon terminals of mechanoreceptors. Their functional significance is controversial and probably includes release of neurotransmitters from afferent axon terminals. Synaptophysin, a major protein of the synaptic vesicle membrane, is present in presynaptic endings of the central and peripheral nervous systems. It is also expressed in mechanosensory neurons which extend into skin forming sensory corpuscles. Nevertheless, synaptophysin occurrence in these structures has never been investigated. Here we used immunohistochemistry to detect synaptophysin in adult human dorsal root ganglia, cutaneous Meissner and Pacinian corpuscles and Merkel cell-neurite complexes from foetal to elderly period. Moreover, we analyzed whether synaptophysin co-localizes with the mechano-gated protein PIEZO2. Synaptophysin immunoreactivity was observed in primary sensory neurons (36 ± 6%) covering the entire soma size ranges. Axons of Meissner's and Pacinian corpuscles were positive for synaptophysin from 36 and 12 weeks of estimated gestational age respectively, to 72 years old. Synaptophysin was also detected in Merkel cells (from 14 weeks of estimated gestational age to old age). Additionally in adult skin, synaptophysin and PIEZO2 co-localized in the axon of Meissner and Pacinian corpuscles, Merkel cells as well as in some axons of Merkel cell-neurite complexes. Present results demonstrate that a subpopulation of primary sensory neurons and their axon terminals forming cutaneous sensory corpuscles contain synaptophysin, a typical presynaptic vesicle protein. Although the functional relevance of these findings is unknown it might be related to neurotransmission mechanisms linked to mechanotransduction.

Sections du résumé

BACKGROUND BACKGROUND
Small clear synaptic-like vesicles fill axon terminals of mechanoreceptors. Their functional significance is controversial and probably includes release of neurotransmitters from afferent axon terminals. Synaptophysin, a major protein of the synaptic vesicle membrane, is present in presynaptic endings of the central and peripheral nervous systems. It is also expressed in mechanosensory neurons which extend into skin forming sensory corpuscles. Nevertheless, synaptophysin occurrence in these structures has never been investigated.
METHODS METHODS
Here we used immunohistochemistry to detect synaptophysin in adult human dorsal root ganglia, cutaneous Meissner and Pacinian corpuscles and Merkel cell-neurite complexes from foetal to elderly period. Moreover, we analyzed whether synaptophysin co-localizes with the mechano-gated protein PIEZO2.
RESULTS RESULTS
Synaptophysin immunoreactivity was observed in primary sensory neurons (36 ± 6%) covering the entire soma size ranges. Axons of Meissner's and Pacinian corpuscles were positive for synaptophysin from 36 and 12 weeks of estimated gestational age respectively, to 72 years old. Synaptophysin was also detected in Merkel cells (from 14 weeks of estimated gestational age to old age). Additionally in adult skin, synaptophysin and PIEZO2 co-localized in the axon of Meissner and Pacinian corpuscles, Merkel cells as well as in some axons of Merkel cell-neurite complexes.
CONCLUSION CONCLUSIONS
Present results demonstrate that a subpopulation of primary sensory neurons and their axon terminals forming cutaneous sensory corpuscles contain synaptophysin, a typical presynaptic vesicle protein. Although the functional relevance of these findings is unknown it might be related to neurotransmission mechanisms linked to mechanotransduction.

Identifiants

pubmed: 35588932
pii: S0940-9602(22)00070-X
doi: 10.1016/j.aanat.2022.151955
pii:
doi:

Substances chimiques

Biomarkers 0
Synaptophysin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

151955

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier GmbH.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that there are no conflicts of interest regarding the publication of this paper.

Auteurs

Yolanda García-Mesa (Y)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

Jorge García-Piqueras (J)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

Patricia Cuendias (P)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

Ramón Cobo (R)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

José Martín-Cruces (J)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

Jorge Feito (J)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain; Servicio de Anatomía Patológica, Complejo Hospitalario Universitario, Salamanca, Spain.

Olivia García-Suarez (O)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain.

Benjamín Martín Biedma (BM)

Departamento de Cirugía y Especialidades Médico-Quirúrgicas, Universidad de Santiago de Compostela, Spain.

J A Vega (JA)

Departamento de Morfología y Biología Celular - Grupo SINPOs, Universidad de Oviedo, Oviedo, Spain; Facutad de Ciencias de la Salud, Universidad Autónoma de Chile, Santiago de Chile, Chile. Electronic address: javega@uniovi.es.

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Classifications MeSH