Devgan Vikram, Nguyen Bach-Cuc, Oh Heysun, Dotto G Paolo
Cutaneous Biology Research Center, Massachusetts General Hospital and Harvard Medical School, Charlestown, Massachusetts 02129, USA.
J Biol Chem. 2006 Oct 13;281(41):30463-70. doi: 10.1074/jbc.M604684200. Epub 2006 Aug 15.
p21 plays a dual role in keratinocyte growth and differentiation control. It restricts the number of keratinocyte stem cell populations while inhibiting the later stages of differentiation independently of the cell cycle. The molecular/biochemical mechanism for the differentiation suppressive function of p21 is unknown. Here we show that elevated p21 expression leads to activation of MAPK family members in a keratinocyte-specific and cell cycle-independent manner, and up-regulation of MAPK activity can explain the inhibitory effects of p21 on differentiation. p21 induces transcription of several genes with MAPK activation potential. Although several of these genes are induced by p21 in a MAPK-dependent manner, expression of IGF-I is induced upstream of MAPK activation. IGF-I stimulation is by itself sufficient to cause MAPK activation and inhibit differentiation and suppression of IGF-I signaling by knock down of the cognate receptor (IGF-R1), diminishing the ability of p21 to activate MAPK and suppress differentiation. Thus, in keratinocytes, the ability of p21 to suppress differentiation can be explained by cell type-specific activation of the MAPK cascade by transcriptional up-regulation of the IGF-I gene.
p21在角质形成细胞生长和分化控制中发挥双重作用。它限制角质形成干细胞群体的数量,同时独立于细胞周期抑制分化后期。p21分化抑制功能的分子/生化机制尚不清楚。在此我们表明,p21表达升高以角质形成细胞特异性且独立于细胞周期的方式导致丝裂原活化蛋白激酶(MAPK)家族成员的激活,并且MAPK活性的上调可以解释p21对分化的抑制作用。p21诱导几个具有MAPK激活潜能的基因转录。虽然这些基因中的几个由p21以MAPK依赖的方式诱导,但胰岛素样生长因子-I(IGF-I)的表达在MAPK激活上游被诱导。IGF-I刺激本身足以引起MAPK激活并抑制分化,通过敲低同源受体(IGF-R1)抑制IGF-I信号传导,会削弱p21激活MAPK和抑制分化的能力。因此,在角质形成细胞中,p21抑制分化的能力可以通过IGF-I基因转录上调对MAPK级联反应的细胞类型特异性激活来解释。