Meyers Jordan M, Grace Miranda, Uberoi Aayushi, Lambert Paul F, Munger Karl
Program in Virology, Harvard Medical School, Boston, MA, United States.
Department of Developmental, Molecular and Chemical Biology, Tufts University School of Medicine, Boston, MA, United States.
Front Microbiol. 2018 Mar 8;9:389. doi: 10.3389/fmicb.2018.00389. eCollection 2018.
Infections with cutaneous papillomaviruses have been linked to cutaneous squamous cell carcinomas that arise in patients who suffer from a rare genetic disorder, epidermodysplasia verruciformis, or those who have experienced long-term, systemic immunosuppression following organ transplantation. The E6 proteins of the prototypical cutaneous human papillomavirus (HPV) 5 and HPV8 inhibit TGF-β and NOTCH signaling. The papillomavirus 1, MmuPV1, infects laboratory mouse strains and causes cutaneous skin warts that can progress to squamous cell carcinomas. MmuPV1 E6 shares biological and biochemical activities with HPV8 E6 including the ability to inhibit TGF-β and NOTCH signaling by binding the SMAD2/SMAD3 and MAML1 transcription factors, respectively. Inhibition of TGF-β and NOTCH signaling is linked to delayed differentiation and sustained proliferation of differentiating keratinocytes. Furthermore, the ability of MmuPV1 E6 to bind MAML1 is necessary for wart and cancer formation in experimentally infected mice. Hence, experimental MmuPV1 infection in mice will be a robust and valuable experimental system to dissect key aspects of cutaneous HPV infection, pathogenesis, and carcinogenesis.
皮肤乳头瘤病毒感染与皮肤鳞状细胞癌有关,这些癌症发生在患有罕见遗传病疣状表皮发育不良的患者身上,或发生在器官移植后经历长期全身免疫抑制的患者身上。典型的皮肤人类乳头瘤病毒(HPV)5和HPV8的E6蛋白可抑制TGF-β和NOTCH信号通路。乳头瘤病毒1(MmuPV1)可感染实验室小鼠品系,并引起皮肤疣,这些疣可发展为鳞状细胞癌。MmuPV1 E6与HPV8 E6具有生物学和生化活性,包括分别通过结合SMAD2/SMAD3和MAML1转录因子来抑制TGF-β和NOTCH信号通路的能力。TGF-β和NOTCH信号通路的抑制与分化角质形成细胞的分化延迟和持续增殖有关。此外,MmuPV1 E6结合MAML1的能力对于实验感染小鼠的疣和癌症形成是必要的。因此,小鼠实验性MmuPV1感染将是一个强大而有价值的实验系统,用于剖析皮肤HPV感染、发病机制和致癌作用的关键方面。