Abstract
To evaluate the developmental distribution of adrenergic cells in vivo, we inserted the Cre-recombinase gene into the locus encoding for the epinephrine biosynthetic enzyme phenylethanolamine n-methyltransferase (Pnmt) and crossed these Pnmt-Cre mice with ROSA26 reporter (R26R) mice to activate LacZ (encoding β-galactosidase) expression in cells that were selectively derived from the adrenergic lineage. Our data show the following: (1) Insertion of Cre-recombinase into the Pnmt locus created a functional knockout of Pnmt expression with concomitant loss of epinephrine in homozygous Pnmt Cre/Cre mice; (2) Despite the reduction in Pnmt expression and epinephrine production in PnmtCre/Cre mice, these mice were viable and fertile, with no apparent developmental defects; (3) When crossed with R26R mice, Pnmt-Cre activation of LacZ expression faithfully recapitulated Pnmt expression in vivo; and (4) LacZ expression was activated in substantial numbers of pacemaking, conduction, and working cardiomyocytes.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 849-858 |
| Number of pages | 10 |
| Journal | Developmental Dynamics |
| Volume | 231 |
| Issue number | 4 |
| DOIs | |
| State | Published - Dec 2004 |
| Externally published | Yes |
Keywords
- Catecholamines
- Epinephrine
- Heart development
- Pacemaking
ASJC Scopus subject areas
- Developmental Biology
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