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Á¢¼ö¹øÈ£ - 890068 RHOP-65 |
Clock Gene Expression in Nasal Mucosa and Their Expression Levels
are Altered in Allergic Rhinitis, Possibly Contributing to Nasal Cycles |
Dept. of Otorhinolaryngology-Head & Neck Surgery, Korea Univ., College of Medicine1,Dept. of Otorhinolaryngology-Head & Neck Surgery, Hallym Univ., College of Medicine2 |
Ha Kyun KIM,
Ha Kyun KIM1,Jin Ho KOOK2,Tae Hoon KIM1,Se Hee LIM1,Sung Hoon KANG1,Sang Hag LEE1,
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¸ñÀû: Allergic rhinitis (AR) is characterized by typical symptoms such
as rhinorrhea, itching, sneezing and nasal blockage. The severity
of nasal congestion follows circardian rhythm, being worst at
night and in the early morning. Sneezing and rhinorrhea secondary
to AR are greater in intensity during morning. The mechanism
involving in circardian rhythm of AR is not clearly understood
yet. We speculate that these symptoms are under control of the
circardian clock. The present study is to investigate the
expression and distribution pattern of clock gene in human and
rat nasal mucosa, and further evaluate the expression levels of
clock gene in mild, and moderate/severe persistent allergic nasal
mucosa. ¹æ¹ý:Clock genes (per1, per2, clock, BMAL1) were evaluated in normal and
allergic nasal mucosa using RT-PCR, real-time PCR,
immunohistochemistry, and western blot. Cultured epithelium derived
from normal turbinates was used to evaluate the effect of
glucocorticoids on the clock genes. The expression levels of clock
genes were evaluated in time series analysis using real time PCR. °á°ú:Cloke genes mRNA and proteins are expressed in normal and allergic nasal mucosa. Their expression levels in mild and moderate/severe persistent allergic nasal mucosa were decreased compared with normal nasal mucosa. The expression levels of clock genes in cultured epithelial cells were increased by glucocorticoids administration. The rhythmical curve of these genes levels were noted in rat nasal mucosa in time-dependent manner. °á·Ð:The present results showed that clock genes (per1, per2, clock,
BMAL1) were present in human and rat nasal mucosa. Deregulated
expression of these genes may participate in the pathogenesis of
allergic nasal mucosa. Furthermore, these genes may possibly
contribute to the development of the nasal cycles. |
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