SHORT PHOTOPERIOD-DEPENDENT DOWN-REGULATION OF THYROTROPIN-ALPHA AND THYROTROPIN-BETA IN HAMSTER PARS-TUBERALIS-SPECIFIC CELLS IS PREVENTEDBY PINEALECTOMY
J. Bockmann et al., SHORT PHOTOPERIOD-DEPENDENT DOWN-REGULATION OF THYROTROPIN-ALPHA AND THYROTROPIN-BETA IN HAMSTER PARS-TUBERALIS-SPECIFIC CELLS IS PREVENTEDBY PINEALECTOMY, Endocrinology, 137(5), 1996, pp. 1804-1813
Hamster hypophyseal pars tuberalis (PT)-specific cells are characteriz
ed by the expression of common alpha-chain and TSH beta. Immuno-reacti
vity for these subunits and the morphology of these cells are known to
exhibit remarkable seasonal changes. The high density of melatonin (M
el) receptors on PT-specific cells leads to the supposition that fluct
uations in circulating Mel levels induced by photoperiodic signals are
a crucial factor for the morphological alterations. To more closely i
nvestigate transcriptional and translational activities in PT-specific
cells, we cloned and sequenced hamster alpha and TSH beta complementa
ry DNA fragments and assessed messenger RNA/protein formation by in si
tu hybridization and immunocytochemistry under short and long photoper
iod and in pinealectomized animals kept in short photoperiod. Hamster
common alpha-chain and TSH beta exhibited high sequence homology with
the corresponding rat hormones [94% (alpha-chain) and 90% (TSH beta) o
n the nucleotide level and 100% (alpha-chain) and 96% (TSH beta) on th
e amino acid level]. Immunocytochemical staining with antibodies direc
ted against the common alpha-chain and TSH beta revealed a reduced imm
unoreactivity of PT-specific cells under short photoperiod, but this w
as not altered in pinealectomized animals exposed to short photoperiod
. In situ hybridization against both hormonal subunits paralleled thes
e changes, with a dramatic decrease in hormonal messenger RNA in short
photoperiod. This regulatory influence was also blocked by pinealecto
my. Taken together, these results demonstrate that; transcription and
translation of hormonal subunits are regulated by photoperiod in hamst
er PT-specific cells, whereas expression remained unchanged in short p
hotoperiod if pinealectomy was performed. We, therefore, conclude that
in hamsters, the Mel signal not the light regimen per se, is a direct
or indirect Zeitgeber for the transduction of photoperiodic informati
on to the secretory activity in this pituitary cell type.