Evidence that β-endorphin is synthesized in cells in the nucleus tractus solitarius: detection of POMC mRNA

DM Bronstein, MKH Schafer, SJ Watson, H Akil - Brain research, 1992 - Elsevier
DM Bronstein, MKH Schafer, SJ Watson, H Akil
Brain research, 1992Elsevier
Evidence from a number of sources indicates that the major site of pro-opiomelanocortin
(POMC)-producing cells in the CNS is the arcuate nucleus of the hypothalamus. Using
immunocytochemical techniques, a second, smaller group of POMC cells has been detected
in the nucleus tractus solitarius (NTS) area of the caudal medulla. However, POMC mRNA
has never been reported in the NTS even though it has been found in other
extrahypothalamic brain regions. Thus, there is some uncertainty as to whether POMC …
Abstract
Evidence from a number of sources indicates that the major site of pro-opiomelanocortin (POMC)-producing cells in the CNS is the arcuate nucleus of the hypothalamus. Using immunocytochemical techniques, a second, smaller group of POMC cells has been detected in the nucleus tractus solitarius (NTS) area of the caudal medulla. However, POMC mRNA has never been reported in the NTS even though it has been found in other extrahypothalamic brain regions. Thus, there is some uncertainty as to whether POMC peptides are actually synthesized de novo in the NTS. In the present study, we used biochemical and anatomical techniques to examine whether POMC mRNA is localized in the NTS. Using in situ hybridization, cells containing POMC mRNA were found in the caudal portion of the NTS. The nucleic acid distribution correlated well with the anatomical distribution of 16k POMC peptide immunoreactivity as determined by immunocytochemistry. Northern analysis revealed that the apparent size of POMC mRNA in the NTS was similar to that found in the arcuate nucleus or the pituitary gland. Results of RNase protection assays using a POMC riboprobe complementary to the 5′ end of exon 3 suggested that POMC mRNA in the NTS and arcuate nucleus are identical in this region of the message at least. We also calculated POMC peptide product to mRNA ratios in different tissues and found that NTS cells appear to produce less peptide per mRNA molecule than those in the arcuate nucleus or pituitary gland. Taken together, these data provide the strongest evidence to date that POMC is synthesized de novo in the NTS and offer support for a role for POMC-derived opioid and non-opioid peptides in autonomic functions in the caudal medulla.
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