Author | dc.contributor.author | Gallardo, Viviana E. | |
Author | dc.contributor.author | Liang, Jin | es_CL |
Author | dc.contributor.author | Behra, Martine | es_CL |
Author | dc.contributor.author | Elkahloun, Abdel | es_CL |
Author | dc.contributor.author | Villablanca, Eduardo J. | es_CL |
Author | dc.contributor.author | Russo, Vincenzo | es_CL |
Author | dc.contributor.author | Allende Connelly, Miguel | es_CL |
Author | dc.contributor.author | Burgess, Shawn M. | es_CL |
Admission date | dc.date.accessioned | 2011-05-19T17:23:45Z | |
Available date | dc.date.available | 2011-05-19T17:23:45Z | |
Publication date | dc.date.issued | 2010-12-13 | |
Cita de ítem | dc.identifier.citation | BMC DEVELOPMENTAL BIOLOGY, Volume: 10, Article Number: 120, 2010 | es_CL |
Identifier | dc.identifier.issn | 1471-213X | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/119207 | |
General note | dc.description | Artículo de publicación ISI | es_CL |
Abstract | dc.description.abstract | Background: Development of the posterior lateral line (PLL) system in zebrafish involves cell migration,
proliferation and differentiation of mechanosensory cells. The PLL forms when cranial placodal cells delaminate and
become a coherent, migratory primordium that traverses the length of the fish to form this sensory system. As it
migrates, the primordium deposits groups of cells called neuromasts, the specialized organs that contain the
mechanosensory hair cells. Therefore the primordium provides both a model for studying collective directional cell
migration and the differentiation of sensory cells from multipotent progenitor cells.
Results: Through the combined use of transgenic fish, Fluorescence Activated Cell Sorting and microarray analysis
we identified a repertoire of key genes expressed in the migrating primordium and in differentiated neuromasts.
We validated the specific expression in the primordium of a subset of the identified sequences by quantitative RTPCR,
and by in situ hybridization. We also show that interfering with the function of two genes, f11r and cd9b,
defects in primordium migration are induced. Finally, pathway construction revealed functional relationships
among the genes enriched in the migrating cell population.
Conclusions: Our results demonstrate that this is a robust approach to globally analyze tissue-specific expression
and we predict that many of the genes identified in this study will show critical functions in developmental events
involving collective cell migration and possibly in pathological situations such as tumor metastasis. | es_CL |
Patrocinador | dc.description.sponsorship | This work was
supported by grants to M.A. from Fondecyt (1070867), ICM (P06-039F) and
FONDAP (15090007). V.G. was supported by a Conicyt fellowship and travel
fellowships from the Vicerrectoría de Asuntos Académicos, Departamento de
Postgrado y Postítulo, Universidad de Chile and MECESUP. This research was
supported by the Intramural Research Program of the National Human
Genome Research Institute, National Institutes of Health (S.B.). | es_CL |
Lenguage | dc.language.iso | en | es_CL |
Publisher | dc.publisher | BIOMED CENTRAL | es_CL |
Keywords | dc.subject | COLLECTIVE CELL-MIGRATION | es_CL |
Título | dc.title | Molecular dissection of the migrating posterior lateral line primordium during early development in zebrafish | es_CL |
Document type | dc.type | Artículo de revista | |