TY - JOUR
T1 - mPer2 antisense oligonucleotides inhibit mPER2 expression but not circadian rhythms of physiological activity in cultured suprachiasmatic nucleus neurons
AU - Sugiyama, Takashi
AU - Yoshioka, Tohru
AU - Ikeda, Masayuki
N1 - Funding Information:
We thank Dr. Charles N. Allen (Oregon Health and Science University) and Dr. Takahiro Moriya (Nagasaki University) for helpful comments on the manuscript. The YC2.1 was a gift from Dr. Atsushi Miyawaki (RIKEN). The NSE promoter was a gift from Dr. Kenji Sakimura (Nigata University). This work is supported in part by Grants-in-Aid for scientific research (B[2]14380372 and B[2]10288053) by the Ministry of Education, Culture, Sports, Science and Technology Japan, to M.I.
PY - 2004/10/15
Y1 - 2004/10/15
N2 - Various day-night rhythms, observed at molecular, cellular, and behavioral levels, are governed by an endogenous circadian clock, predominantly functioning in the hypothalamic suprachiasmatic nucleus (SCN). A class of clock genes, mammalian Period (mPer), is known to be rhythmically expressed in SCN neurons, but the correlation between mPER protein levels and autonomous rhythmic activity in SCN neurons is not well understood. Therefore, we blocked mPer translation using antisense phosphothioate oligonucleotides (ODNs) for mPer1 and mPer2 mRNAs and examined the effects on the circadian rhythm of cytosolic Ca 2+ concentration and action potentials in SCN slice cultures. Treatment with mPer2 ODNs (20 μM for 3 days) but not randomized control ODNs significantly reduced mPER2 immunoreactivity (-63%) in the SCN. Nevertheless, mPer1/2 ODNs treatment inhibited neither action potential firing rhythms nor cytosolic Ca 2+ rhythms. These suggest that circadian rhythms in mPER protein levels are not necessarily coupled to autonomous rhythmic activity in SCN neurons.
AB - Various day-night rhythms, observed at molecular, cellular, and behavioral levels, are governed by an endogenous circadian clock, predominantly functioning in the hypothalamic suprachiasmatic nucleus (SCN). A class of clock genes, mammalian Period (mPer), is known to be rhythmically expressed in SCN neurons, but the correlation between mPER protein levels and autonomous rhythmic activity in SCN neurons is not well understood. Therefore, we blocked mPer translation using antisense phosphothioate oligonucleotides (ODNs) for mPer1 and mPer2 mRNAs and examined the effects on the circadian rhythm of cytosolic Ca 2+ concentration and action potentials in SCN slice cultures. Treatment with mPer2 ODNs (20 μM for 3 days) but not randomized control ODNs significantly reduced mPER2 immunoreactivity (-63%) in the SCN. Nevertheless, mPer1/2 ODNs treatment inhibited neither action potential firing rhythms nor cytosolic Ca 2+ rhythms. These suggest that circadian rhythms in mPER protein levels are not necessarily coupled to autonomous rhythmic activity in SCN neurons.
KW - Ca imaging
KW - Glutamic acid decarboxylase
KW - Immunofluorescent staining
KW - Mouse
KW - Per1
KW - Per2
UR - http://www.scopus.com/inward/record.url?scp=4544372208&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2004.08.126
DO - 10.1016/j.bbrc.2004.08.126
M3 - 学術論文
C2 - 15369776
AN - SCOPUS:4544372208
SN - 0006-291X
VL - 323
SP - 479
EP - 483
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -