Interaction between axons and specific populations of surrounding cells is indispensable for collateral formation in the mammillary system

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Background: An essential phenomenon during brain development is the extension of long collateral branches by axons. How the local cellular environment contributes to the initial sprouting of these branches in specific points of an axonal shaft remains unclear. Methodology/Principal Findings: The principal mammillary tract (pm) is a landmark axonal bundle connecting ventral diencephalon to brainstem (through the mammillotegmental tract, mtg). Late in development, the axons of the principal mammillary tract sprout collateral branches at a very specific point forming a large bundle whose target is the thalamus. Inspection of this model showed a number of distinct, identified cell populations originated in the dorsal and the ventral diencephalon and migrating during development to arrange themselves into several discrete groups around the branching point. Further analysis of this system in several mouse lines carrying mutant alleles of genes expressed in defined subpopulations (including Pax6, Foxb1, Lrp6 and Gbx2) together with the use of an unambiguous genetic marker of mammillary axons revealed: 1) a specific group of Pax6-expressing cells in close apposition with the prospective branching point is indispensable to elicit axonal branching in this system; and 2) cooperation of transcription factors Foxb1 and Pax6 to differentially regulate navigation and fasciculation of distinct branches of the principal mammillary tract. Conclusions/Significance: Our results define for the first time a model system where interaction of the axonal shaft with a specific group of surrounding cells is essential to promote branching. Additionally, we provide insight on the cooperative transcriptional regulation necessary to promote and organize an intricate axonal tree. © 2011 Szabó et al.

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dc.contributor.authorSzabó, Nora-Emöke
dc.contributor.authorZhao, Tianyu
dc.contributor.authorÇankaya, Murat
dc.contributor.authorStoykova, Anastassia
dc.contributor.authorZhou, Xunlei
dc.contributor.authorAlvarez-Bolado, Gonzalo
dc.date.accessioned2026-10-18T20:30:46.797135677Z
dc.date.available2026-10-18T20:30:46.797135677Z
dc.date.issued2011
dc.description.abstractBackground: An essential phenomenon during brain development is the extension of long collateral branches by axons. How the local cellular environment contributes to the initial sprouting of these branches in specific points of an axonal shaft remains unclear. Methodology/Principal Findings: The principal mammillary tract (pm) is a landmark axonal bundle connecting ventral diencephalon to brainstem (through the mammillotegmental tract, mtg). Late in development, the axons of the principal mammillary tract sprout collateral branches at a very specific point forming a large bundle whose target is the thalamus. Inspection of this model showed a number of distinct, identified cell populations originated in the dorsal and the ventral diencephalon and migrating during development to arrange themselves into several discrete groups around the branching point. Further analysis of this system in several mouse lines carrying mutant alleles of genes expressed in defined subpopulations (including Pax6, Foxb1, Lrp6 and Gbx2) together with the use of an unambiguous genetic marker of mammillary axons revealed: 1) a specific group of Pax6-expressing cells in close apposition with the prospective branching point is indispensable to elicit axonal branching in this system; and 2) cooperation of transcription factors Foxb1 and Pax6 to differentially regulate navigation and fasciculation of distinct branches of the principal mammillary tract. Conclusions/Significance: Our results define for the first time a model system where interaction of the axonal shaft with a specific group of surrounding cells is essential to promote branching. Additionally, we provide insight on the cooperative transcriptional regulation necessary to promote and organize an intricate axonal tree. © 2011 Szabó et al.
dc.description.sponsorshipWork was supported by the Max Planck Society and by the Deutsche Forschungsgemeinschaft Grant AL 603. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Andrea Wizenmann (University of Tubingen) and Herbert Hildebrandt (University of Hannover) made valuable comments on the text. Michael Heide (University of Heidelberg) assisted with the confocal microscopy. The anti-Pax6 antibody, developed by A. Kawakami, was obtained from the Developmental Studies Hybridoma Bank developed under the auspices of the NICHD and maintained by The University of Iowa, Department of Biology, Iowa City, IA 52242.
dc.identifier.doi10.1371/journal.pone.0020315
dc.identifier.issn1932-6203
dc.identifier.issue5
dc.identifier.pmid21625468
dc.identifier.scopus2-s2.0-79956327231
dc.identifier.startpagee20315
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15934
dc.identifier.volume6
dc.identifier.wosWOS:000290793400055
dc.language.isoen
dc.publisherPUBLIC LIBRARY SCIENCE
dc.relation.ispartofPLoS ONE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnimals
dc.subjectAxons
dc.subjectEye Proteins
dc.subjectGene Expression Profiling
dc.subjectHomeodomain Proteins
dc.subjectImmunohistochemistry
dc.subjectIn Situ Hybridization
dc.subjectMamillary Bodies
dc.subjectMice
dc.subjectMice, Mutant Strains
dc.subjectMicroscopy, Confocal
dc.subjectPaired Box Transcription Factors
dc.subjectRepressor Proteins
dc.subjecteye protein
dc.subjecthomeodomain protein
dc.subjectpaired box transcription factor
dc.subjectrepressor protein
dc.subjecttranscription factor PAX6
dc.subjectanimal tissue
dc.subjectarticle
dc.subjectbrain development
dc.subjectbrain stem
dc.subjectcell migration
dc.subjectcell population
dc.subjectcontrolled study
dc.subjectdiencephalon
dc.subjectembryo
dc.subjectfemale
dc.subjectFoxb1 gene
dc.subjectGbx2 gene
dc.titleInteraction between axons and specific populations of surrounding cells is indispensable for collateral formation in the mammillary system
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus9
rdl.citation.wos9
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)