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Pax-2 is required for mesenchyme-to-epithelium
conversion during kidney development. Rothenpieler
UW, Dressler GR Development 1993 Nov;119(3):711-20
- The conversion of mesenchyme to epithelium during the
embryonic development of the mammalian kidney requires
reciprocal inductive interactions between the ureter and
the responding metanephric mesenchyme. The Pax-2 gene is
activated in the mesenchyme in response to induction and
is subsequently down-regulated in more differentiated
cells derived from the mesenchyme. Pax-2 belongs to a
family of genes, at least three of which encode
morphogenetic regulatory transcription factors. In order
to determine the role of Pax-2 during kidney development,
we have generated a loss-of-function phenotype using
antisense oligonucleotides in mouse kidney organ
cultures. These oligonucleotides can specifically inhibit
Pax-2 protein accumulation in kidney mesenchyme cells,
where the intracellular concentrations are maximal. The
kidney organ cultures were stained with uvomurulin and
laminin antibodies as markers for epithelium formation.
With significantly reduced Pax-2 protein levels, kidney
mesenchyme cells fail to aggregate and do not undergo the
sequential morphological changes characteristic of
epithelial cell formation. The data demonstrate that
Pax-2 function is required for the earliest phase of
mesenchyme-to-epithelium conversion.
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