fast-efficient-expression-multiple-proteins-avian-embryos-using-mrna

Fast and Efficient Expression of Multiple Proteins in Avian Embryos Using mRNA Electroporation

We report that mRNA electroporation permits fluorescent proteins to label cells in living quail embryos more quickly and broadly than DNA electroporation. ...

Children's Hospital Los Angeles

University of Southern California, Los Angeles

During early avian development, primordial germ cells (PGC) are highly migratory, moving from the central area pellucida of the blastoderm to the anterior extra-embryonic germinal crescent. The PGCs soon move into the forming blood vessels by intravasation and travel in the circulatory system to the genital ridges where they participate in the organogenesis of the gonads. This complex cellular migration takes place in close association with a nascent extracellular matrix that matures in a precise spatio-temporal pattern. We first compiled a list of quail matrisome genes by bioinformatic screening of human matrisome orthologs. Next, we used single cell RNA-seq analysis (scRNAseq) to determine that PGCs express numerous ECM and ECM-associated genes in early embryos. The expression of select ECM transcripts and proteins in PGCs were verified by fluorescent  hybridization (FISH) and immunofluorescence (IF). Live imaging of transgenic quail embryos injected with fluorescent antibodies against fibronectin and laminin, showed that germinal crescent PGCs display rapid shape changes and morphological properties such as blebbing and filopodia while surrounded by, or in close contact with, an ECM fibril meshwork that is itself in constant motion. Injection of anti-β1 integrin CSAT antibodies resulted in a reduction of mature fibronectin and laminin fibril meshwork in the germinal crescent at HH4-5 but did not alter the active motility of the PGCs or their ability to populate the germinal crescent. These results suggest that integrin β1 receptors are important, but not required, for PGCs to successfully migrate during embryonic development, but instead play a vital role in ECM fibrillogenesis and assembly.

Mohit Dave

Department of Radiology and Developmental Neuroscience Program,
Saban Research Institute,
Department of Radiology and Developmental Neuroscience Program, Saban Research Institute

Children's Hospital Los Angeles

Fast and Efficient Expression of Multiple Proteins in Avian Embryos Using mRNA Electroporation

Mohit Dave

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Radiology and Developmental Neuroscience Program,Saban Research Institute,Department of Radiology and Developmental Neuroscience Program, Saban Research Institute

Children's Hospital Los Angeles

Fast and Efficient Expression of Multiple Proteins in Avian Embryos Using mRNA Electroporation

Department of Radiology and Developmental Neuroscience Program,
Saban Research Institute,
Department of Radiology and Developmental Neuroscience Program, Saban Research Institute