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ECB-ART-48869
Exp Anim 2021 Aug 06;703:378-386. doi: 10.1538/expanim.21-0001.
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Human disease-associated extracellular matrix orthologs ECM3 and QBRICK regulate primary mesenchymal cell migration in sea urchin embryos.

Kiyozumi D , Yaguchi S , Yaguchi J , Yamazaki A , Sekiguchi K .


Abstract
Sea urchin embryos have been one of model organisms to investigate cellular behaviors because of their simple cell composition and transparent body. They also give us an opportunity to investigate molecular functions of human proteins of interest that are conserved in sea urchin. Here we report that human disease-associated extracellular matrix orthologues ECM3 and QBRICK are necessary for mesenchymal cell migration during sea urchin embryogenesis. Immunofluorescence has visualized the colocalization of QBRICK and ECM3 on both apical and basal surface of ectoderm. On the basal surface, QBRICK and ECM3 constitute together a mesh-like fibrillar structure along the blastocoel wall. When the expression of ECM3 was knocked down by antisense-morpholino oligonucleotides, the ECM3-QBRICK fibrillar structure completely disappeared. When QBRICK was knocked down, the ECM3 was still present, but the basally localized fibers became fragmented. The ingression and migration of primary mesenchymal cells were not critically affected, but their migration at later stages was severely affected in both knock-down embryos. As a consequence of impaired primary mesenchymal cell migration, improper spicule formation was observed. These results indicate that ECM3 and QBRICK are components of extracellular matrix, which play important role in primary mesenchymal cell migration, and that sea urchin is a useful experimental animal model to investigate human disease-associated extracellular matrix proteins.

PubMed ID: 33828019
PMC ID: PMC8390315
Article link: Exp Anim


Genes referenced: LOC100887844 LOC115919910
Morpholinos: LOC115922229 MO1 LOC115922229 MO2 LOC115922229 MO3 LOC579397 MO1 LOC579397 MO2


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References [+] :
Alazami, FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome. 2009, Pubmed