De Laurenzi V, Rossi A, Terrinoni A, Barcaroli D, Levrero M, Costanzo A, Knight R A, Guerrieri P, Melino G
Biochemistry Laboratory, Tor Vergata University, Rome, 00133, Italy.
Biochem Biophys Res Commun. 2000 Jun 24;273(1):342-6. doi: 10.1006/bbrc.2000.2932.
p53 and its two homologues, p73 and p63, share considerable structural similarities, an ability to interact between themselves and to transactivate the same promoters, including for example p21. Furthermore, p73 can induce cell death via its interaction with c-Abl. In contrast, p63 has been demonstrated to be essential for limb and skin formation. We evaluated the expression of p63 and p73 in differentiating human keratinocytes in vitro. Skin biopsy and primary cultures of normal human epidermal keratinocytes (NHEK) express both p73 and p63. NHEK induced to differentiate in vitro by high calcium exposure show induction of p73 delta and downregulation of all isoforms of p63. This latter gene is predominantly expressed in its transcriptionally inactive form, DeltaNp63. We further evaluated the effect of either p73s or p63 transfected in either NHEK or transformed human keratinocytes (HaCat cells). p73 gamma, delta, and p63 were able to transactivate the promoters of loricrin and involucrin in both NHEK and HaCat cells. These results suggest the involvement of both p73 and p63 genes in keratinocyte terminal differentiation.
p53及其两个同源物p73和p63具有相当大的结构相似性,它们之间能够相互作用并反式激活相同的启动子,例如p21的启动子。此外,p73可通过与c-Abl相互作用诱导细胞死亡。相比之下,p63已被证明对肢体和皮肤形成至关重要。我们评估了p63和p73在体外分化的人角质形成细胞中的表达。皮肤活检以及正常人表皮角质形成细胞(NHEK)的原代培养物均表达p73和p63。通过高钙暴露诱导体外分化的NHEK显示p73δ的诱导以及p63所有异构体的下调。后一个基因主要以其转录无活性形式DeltaNp63表达。我们进一步评估了在NHEK或转化的人角质形成细胞(HaCat细胞)中转入p73或p63的效果。p73γ、δ和p63能够在NHEK和HaCat细胞中反式激活loricrin和involucrin的启动子。这些结果表明p73和p63基因均参与角质形成细胞的终末分化。