Department of Medical Genetics, Haukeland University Hospital, 5021, Bergen, Norway.
Department of Ophthalmology, Haukeland University Hospital, 5021, Bergen, Norway.
Eur J Hum Genet. 2019 Apr;27(4):574-581. doi: 10.1038/s41431-018-0323-z. Epub 2018 Dec 20.
Missense variants located to the "molecular brake" in the tyrosine kinase hinge region of platelet-derived growth factor receptor-β, encoded by PFGFRB, can cause Penttinen-type (Val665Ala) and Penttinen-like (Asn666His) premature ageing syndromes, as well as infantile myofibromatosis (Asn666Lys and Pro660Thr). We have found the same de novo PDGFRB c.1997A>G p.(Asn666Ser) variants in two patients with lipodystrophy, acro-osteolysis and severely reduced vision due to corneal neovascularisation, reminiscent of a severe form of Penttinen syndrome with more pronounced connective tissue destruction. In line with this phenotype, patient skin fibroblasts were prone to apoptosis. Both in patient fibroblasts and stably transduced HeLa and HEK293 cells, autophosphorylation of PDGFRβ was observed, as well as increased phosphorylation of downstream signalling proteins such as STAT1, PLCγ1, PTPN11/SHP2-Tyr580 and AKT. Phosphorylation of MAPK3 (ERK1) and PTPN11/SHP2-Tyr542 appeared unaffected. This suggests that this missense change not only weakens tyrosine kinase autoinhibition, but also influences substrate binding, as both PTPN11 tyrosines (Tyr542 and Tyr580) usually are phosphorylated upon PDGFR activation. Imatinib was a strong inhibitor of phosphorylation of all these targets, suggesting an option for precision medicine based treatment.
错义变异位于血小板衍生生长因子受体-β(PDGFRB)编码的酪氨酸激酶铰链区的“分子刹车”中,可导致 Penttinen 型(Val665Ala)和 Penttinen 样(Asn666His)早衰综合征,以及婴儿肌纤维瘤病(Asn666Lys 和 Pro660Thr)。我们在两名脂肪营养不良、肢端骨溶解和严重视力下降(由于角膜新生血管化)的患者中发现了相同的 PDGFRB c.1997A>G p.(Asn666Ser)变体,类似于 Penttinen 综合征的严重形式,伴有更明显的结缔组织破坏。与这种表型一致,患者皮肤成纤维细胞容易发生细胞凋亡。在患者成纤维细胞和稳定转导的 HeLa 和 HEK293 细胞中,均观察到 PDGFRβ的自动磷酸化,以及下游信号蛋白如 STAT1、PLCγ1、PTPN11/SHP2-Tyr580 和 AKT 的磷酸化增加。MAPK3(ERK1)和 PTPN11/SHP2-Tyr542 的磷酸化似乎不受影响。这表明这种错义变化不仅削弱了酪氨酸激酶的自动抑制作用,还影响了底物结合,因为 PDGFR 激活后通常会磷酸化 PTPN11 的两个酪氨酸(Tyr542 和 Tyr580)。伊马替尼强烈抑制所有这些靶标的磷酸化,这表明基于精准医学的治疗选择。