PT  - JOURNAL ARTICLE
AU  - Ren-Xue Wang
AU  - Lee E. Limbird
TI  - Distribution of mRNA Encoding Three α<sub>2</sub>-Adrenergic Receptor Subtypes in the Developing Mouse Embryo Suggests a Role for the α<sub>2A</sub> Subtype in Apoptosis
AID  - 10.1124/mol.52.6.1071
DP  - 1997 Dec 01
TA  - Molecular Pharmacology
PG  - 1071--1080
VI  - 52
IP  - 6
4099  - http://molpharm.aspetjournals.org/content/52/6/1071.short
4100  - http://molpharm.aspetjournals.org/content/52/6/1071.full
SO  - Mol Pharmacol1997 Dec 01; 52
AB  - α2-Adrenergic receptors (α2-ARs) respond to norepinephrine and epinephrine to mediate diverse physiological effects. Using in situ hybridization, the expression pattern of the mRNA encoding the three α2-AR subtypes (α2A, α2B, and α2C) was examined in the mouse embryo. The mRNA encoding the three subtypes was first detected at stage 9.5 days postcoitus (d.p.c.) for the α2A-AR (coincident with norepinephrine availability), 11.5 d.p.c. for the α2B-AR, and 14.5 d.p.c. for the α2C-AR subtype. The mRNA encoding the α2A-AR subtype shows both the earliest and the most widespread expression pattern, including developing stomach and cecum, many craniofacial regions and areas in the central nervous system. Strikingly, the α2A-AR mRNA is expressed in the interdigital mesenchyme between stage 12.5 and 14.5 d.p.c. in parallel with digit separation, raising the possibility that the α2A-AR might contribute to the apoptotic events underlying this process. To test whether α2A-AR can signal apoptotic events, the α2A-AR subtype was introduced into two mouse mesenchymal cell lines, C3H/10t½ and NIH-3T3; expression of the α2A-AR correlated with accelerated apoptosis, as detected both by the TUNEL assay and the loss of cell viability. In contrast to the wide distribution of mRNA encoding the α2A-AR subtype, the α2B-AR mRNA was detected only in the developing liver and was most readily detectable between 11.5 and 14.5 d.p.c., when the liver is the principal site of hematopoiesis. The α2C-AR mRNA is detected in the nasal cavity and cerebellar primordium only at ≥14.5 d.p.c. These studies represent the first characterization of the temporal and spatial expressions of the α2A-AR, α2B-AR, and α2C-AR subtypes during embryogenesis and provide important insights concerning the loci and possible roles of α2-AR-mediated regulation of physiological processes during the developmental program.