Melatonin inhibits embryonic salivary gland branching morphogenesis by regulating both epithelial cell adhesion and morphology.
Melatonin inhibits embryonic salivary gland branching morphogenesis by regulating both epithelial cell adhesion and morphology.
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DOI:
10.1371/journal.pone.0119960
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Sakai T
中科院分区:
文献类型:
--
作者:
Obana-Koshino A;Ono H;Miura J;Sakai M;Uchida H;Nakamura W;Nohara K;Maruyama Y;Hattori A;Sakai T
Many organs, including salivary glands, lung, and kidney, are formed by epithelial branching during embryonic development. Branching morphogenesis occurs via either local outgrowths or the formation of clefts that subdivide epithelia into buds. This process is promoted by various factors, but the mechanism of branching morphogenesis is not fully understood. Here we have defined melatonin as a potential negative regulator or “brake” of branching morphogenesis, shown that the levels of it and its receptors decline when branching morphogenesis begins, and identified the process that it regulates. Melatonin has various physiological functions, including circadian rhythm regulation, free-radical scavenging, and gonadal development. Furthermore, melatonin is present in saliva and may have an important physiological role in the oral cavity. In this study, we found that the melatonin receptor is highly expressed on the acinar epithelium of the embryonic submandibular gland. We also found that exogenous melatonin reduces salivary gland size and inhibits branching morphogenesis. We suggest that this inhibition does not depend on changes in either proliferation or apoptosis, but rather relates to changes in epithelial cell adhesion and morphology. In summary, we have demonstrated a novel function of melatonin in organ formation during embryonic development.
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影响因子:
10.3
作者:
Martínez-Campa, C;Alonso-González, C;Sánchez-Barceló, EJ
通讯作者:
Sánchez-Barceló, EJ
DOI:
10.1126/science.1191880
发表时间:
2010-07-30
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Onodera T;Sakai T;Hsu JC;Matsumoto K;Chiorini JA;Yamada KM
通讯作者:
Yamada KM
影响因子:
10.3
作者:
Jung-Hynes B;Schmit TL;Reagan-Shaw SR;Siddiqui IA;Mukhtar H;Ahmad N
通讯作者:
Ahmad N
影响因子:
14
作者:
Miyajima, Hiroyuki;Matsumoto, Takuya;Imazato, Satoshi
通讯作者:
Imazato, Satoshi
影响因子:
6.1
作者:
Naji, L;Canillo-Vico, A;Calvo, JR
通讯作者:
Calvo, JR