表皮(动物学)
生物
细胞生物学
角质形成细胞
毛囊
形态发生
信号转导
蛋白激酶A
皮肤当量
表型
细胞凋亡
细胞分化
激酶
体外
遗传学
解剖
基因
作者
Matthias Drosten,Carmen G. Lechuga,Mariano Barbacid
出处
期刊:Oncogene
[Springer Nature]
日期:2013-07-08
卷期号:33 (22): 2857-2865
被引量:40
摘要
Proliferation in the epidermis is a tightly controlled process. During skin development, epidermis formation and hair follicle morphogenesis crucially depend on the regulated balance between proliferation and differentiation. Here we deleted all three Ras loci (H-Ras, N-Ras and K-Ras) from keratinocytes in vitro as well as specifically from the epidermis in mice using a K5Cre strain. Upon Ras elimination, keratinocytes ceased proliferation and entered into senescence without any signs of apoptosis induction. Constitutive activation of the mitogen-activated protein kinase pathway was able to partially rescue the proliferative defects. In mice, Ras signaling was essential for proper development of the epidermis and hair follicles. Deletion of the three Ras loci during epidermis formation in mouse embryos caused a dramatic decrease in proliferation, resulting in a substantially thinner epidermis and delayed appearance of differentiation markers. We could not detect apoptotic or senescent cells in these embryos suggesting that loss of Ras protein expression only leads to severe hypoproliferation. These observations provide genetic evidence for an essential role of Ras proteins in the control of keratinocyte and epidermal proliferation.
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