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Receptor complexes for each of the Class 3 Semaphorins

The Class 3 Semaphorins (Sema3s) are a sub-family of proteins whose known biological roles are varied and growing. The mechanism of action of the Sema3s requires binding to transmembrane receptors that comprise heteromeric complexes of Neuropilins, Plexins and cell adhesion molecules (CAMs). However...

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Detalles Bibliográficos
Autores principales: Sharma, Anil, Verhaagen, Joost, Harvey, Alan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389612/
https://www.ncbi.nlm.nih.gov/pubmed/22783168
http://dx.doi.org/10.3389/fncel.2012.00028
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author Sharma, Anil
Verhaagen, Joost
Harvey, Alan R.
author_facet Sharma, Anil
Verhaagen, Joost
Harvey, Alan R.
author_sort Sharma, Anil
collection PubMed
description The Class 3 Semaphorins (Sema3s) are a sub-family of proteins whose known biological roles are varied and growing. The mechanism of action of the Sema3s requires binding to transmembrane receptors that comprise heteromeric complexes of Neuropilins, Plexins and cell adhesion molecules (CAMs). However, knowledge of the receptor components of the Sema3s remains incomplete, and there may be receptor components which are as yet undiscovered. The receptor complexes of the Sema3s share receptor components with each other, and it is the specific combination of these components within a heteromeric complex that is thought to give rise to selective binding and signalling for individual Sema3s. This crosstalk makes it experimentally difficult to define a single holoreceptor for each Sema3. Furthermore, the receptor composition for a given Sema3 may differ between cell types, and change as a function of developmental state or pathological situation. Nevertheless, there are at least some known differences in the constitutive structure of the receptors for the Sema3s. For example in neural cells, Sema3a and Sema3f signal through different Neuropilins (Nrp1 and Nrp2 respectively) and L1cam only appears important for Sema3a signaling, while Nrcam forms a complex with Nrp2. Further complexity arises from crosstalk of other families of ligands (e.g., VEGF) with Sema3 receptor components. Thus the Sema3s, which have been shown as antagonists for each other, can also act as antagonists for other families of molecules. This review compiles experimental evidence describing the receptor components for the Sema3s, detailing the current state of knowledge of which components are important for signaling of each Sema3 before going on to consider possible future directions for the field.
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spelling pubmed-33896122012-07-10 Receptor complexes for each of the Class 3 Semaphorins Sharma, Anil Verhaagen, Joost Harvey, Alan R. Front Cell Neurosci Neuroscience The Class 3 Semaphorins (Sema3s) are a sub-family of proteins whose known biological roles are varied and growing. The mechanism of action of the Sema3s requires binding to transmembrane receptors that comprise heteromeric complexes of Neuropilins, Plexins and cell adhesion molecules (CAMs). However, knowledge of the receptor components of the Sema3s remains incomplete, and there may be receptor components which are as yet undiscovered. The receptor complexes of the Sema3s share receptor components with each other, and it is the specific combination of these components within a heteromeric complex that is thought to give rise to selective binding and signalling for individual Sema3s. This crosstalk makes it experimentally difficult to define a single holoreceptor for each Sema3. Furthermore, the receptor composition for a given Sema3 may differ between cell types, and change as a function of developmental state or pathological situation. Nevertheless, there are at least some known differences in the constitutive structure of the receptors for the Sema3s. For example in neural cells, Sema3a and Sema3f signal through different Neuropilins (Nrp1 and Nrp2 respectively) and L1cam only appears important for Sema3a signaling, while Nrcam forms a complex with Nrp2. Further complexity arises from crosstalk of other families of ligands (e.g., VEGF) with Sema3 receptor components. Thus the Sema3s, which have been shown as antagonists for each other, can also act as antagonists for other families of molecules. This review compiles experimental evidence describing the receptor components for the Sema3s, detailing the current state of knowledge of which components are important for signaling of each Sema3 before going on to consider possible future directions for the field. Frontiers Media S.A. 2012-07-05 /pmc/articles/PMC3389612/ /pubmed/22783168 http://dx.doi.org/10.3389/fncel.2012.00028 Text en Copyright © 2012 Sharma, Verhaagen and Harvey. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Sharma, Anil
Verhaagen, Joost
Harvey, Alan R.
Receptor complexes for each of the Class 3 Semaphorins
title Receptor complexes for each of the Class 3 Semaphorins
title_full Receptor complexes for each of the Class 3 Semaphorins
title_fullStr Receptor complexes for each of the Class 3 Semaphorins
title_full_unstemmed Receptor complexes for each of the Class 3 Semaphorins
title_short Receptor complexes for each of the Class 3 Semaphorins
title_sort receptor complexes for each of the class 3 semaphorins
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3389612/
https://www.ncbi.nlm.nih.gov/pubmed/22783168
http://dx.doi.org/10.3389/fncel.2012.00028
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