Transmembrane semaphorins, forward and reverse signaling: have a look both ways
- PMID: 26794845
- DOI: 10.1007/s00018-016-2137-x
Transmembrane semaphorins, forward and reverse signaling: have a look both ways
Abstract
Semaphorins are signaling molecules playing pivotal roles not only as axon guidance cues, but are also involved in the regulation of a range of biological processes, such as immune response, angiogenesis and invasive tumor growth. The main functional receptors for semaphorins are plexins, which are large single-pass transmembrane molecules. Semaphorin signaling through plexins-the "classical" forward signaling-affects cytoskeletal remodeling and integrin-dependent adhesion, consequently influencing cell migration. Intriguingly, semaphorins and plexins can interact not only in trans, but also in cis, leading to differentiated and highly regulated signaling outputs. Moreover, transmembrane semaphorins can also mediate a so-called "reverse" signaling, by acting not as ligands but rather as receptors, and initiate a signaling cascade through their own cytoplasmic domains. Semaphorin reverse signaling has been clearly demonstrated in fruit fly Sema1a, which is required to control motor axon defasciculation and target recognition during neuromuscular development. Sema1a invertebrate semaphorin is most similar to vertebrate class-6 semaphorins, and examples of semaphorin reverse signaling in mammalians have been described for these family members. Reverse signaling is also reported for other vertebrate semaphorin subsets, e.g. class-4 semaphorins, which bear potential PDZ-domain interaction motifs in their cytoplasmic regions. Therefore, thanks to their various signaling abilities, transmembrane semaphorins can play multifaceted roles both in developmental processes and in physiological as well as pathological conditions in the adult.
Keywords: Bidirectional signaling; CNS; Cancer; Heart; Neuron; Retina; Spinal cord.
Similar articles
-
Transmembrane semaphorins: Multimodal signaling cues in development and cancer.Cell Adh Migr. 2016 Nov;10(6):675-691. doi: 10.1080/19336918.2016.1197479. Epub 2016 Jun 13. Cell Adh Migr. 2016. PMID: 27295627 Free PMC article. Review.
-
Boundary cap cells constrain spinal motor neuron somal migration at motor exit points by a semaphorin-plexin mechanism.Neural Dev. 2007 Oct 30;2:21. doi: 10.1186/1749-8104-2-21. Neural Dev. 2007. PMID: 17971221 Free PMC article.
-
Plexin a-semaphorin-1a reverse signaling regulates photoreceptor axon guidance in Drosophila.J Neurosci. 2010 Sep 8;30(36):12151-6. doi: 10.1523/JNEUROSCI.1494-10.2010. J Neurosci. 2010. PMID: 20826677 Free PMC article.
-
Sema-1a Reverse Signaling Promotes Midline Crossing in Response to Secreted Semaphorins.Cell Rep. 2017 Jan 3;18(1):174-184. doi: 10.1016/j.celrep.2016.12.027. Cell Rep. 2017. PMID: 28052247 Free PMC article.
-
Diverse roles for semaphorin-plexin signaling in the immune system.Trends Immunol. 2012 Mar;33(3):127-35. doi: 10.1016/j.it.2012.01.008. Epub 2012 Feb 9. Trends Immunol. 2012. PMID: 22325954 Review.
Cited by
-
Semaphorin-6D and Plexin-A1 Act in a Non-Cell-Autonomous Manner to Position and Target Retinal Ganglion Cell Axons.J Neurosci. 2023 Aug 9;43(32):5769-5778. doi: 10.1523/JNEUROSCI.0072-22.2023. Epub 2023 Jun 21. J Neurosci. 2023. PMID: 37344233 Free PMC article.
-
SEMA6C: a novel adhesion-independent FAK and YAP activator, required for cancer cell viability and growth.Cell Mol Life Sci. 2023 Mar 31;80(4):111. doi: 10.1007/s00018-023-04756-1. Cell Mol Life Sci. 2023. PMID: 37002363 Free PMC article.
-
Semaphorin signaling restricts neuronal regeneration in C. elegans.Front Cell Dev Biol. 2022 Oct 17;10:814160. doi: 10.3389/fcell.2022.814160. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36325362 Free PMC article.
-
Cytotoxic capability and the associated proteomic profile of cell-free coelomic fluid extracts from the edible sea cucumber Holothuria tubulosa on HepG2 liver cancer cells.EXCLI J. 2022 Apr 25;21:722-743. doi: 10.17179/excli2022-4825. eCollection 2022. EXCLI J. 2022. PMID: 35721581 Free PMC article.
-
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance.Hum Mol Genet. 2022 Sep 29;31(19):3325-3340. doi: 10.1093/hmg/ddac114. Hum Mol Genet. 2022. PMID: 35604360 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
