人类腺苷酸激酶2缺乏会导致与感音神经性耳聋相关的严重造血缺陷。
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.
作者信息
Lagresle-Peyrou Chantal, Six Emmanuelle M, Picard Capucine, Rieux-Laucat Frédéric, Michel Vincent, Ditadi Andrea, Demerens-de Chappedelaine Corinne, Morillon Estelle, Valensi Françoise, Simon-Stoos Karen L, Mullikin James C, Noroski Lenora M, Besse Céline, Wulffraat Nicolas M, Ferster Alina, Abecasis Manuel M, Calvo Fabien, Petit Christine, Candotti Fabio, Abel Laurent, Fischer Alain, Cavazzana-Calvo Marina
机构信息
Research Laboratory on Normal and Pathologic Development of the Immune System, U768, Institut National de la Santé et de la Recherche Médicale, 75015 Paris, France.
出版信息
Nat Genet. 2009 Jan;41(1):106-11. doi: 10.1038/ng.278. Epub 2008 Nov 30.
Reticular dysgenesis is an autosomal recessive form of human severe combined immunodeficiency characterized by an early differentiation arrest in the myeloid lineage and impaired lymphoid maturation. In addition, affected newborns have bilateral sensorineural deafness. Here we identify biallelic mutations in AK2 (adenylate kinase 2) in seven individuals affected with reticular dysgenesis. These mutations result in absent or strongly decreased protein expression. We then demonstrate that restoration of AK2 expression in the bone marrow cells of individuals with reticular dysgenesis overcomes the neutrophil differentiation arrest, underlining its specific requirement in the development of a restricted set of hematopoietic lineages. Last, we establish that AK2 is specifically expressed in the stria vascularis region of the inner ear, which provides an explanation of the sensorineural deafness in these individuals. These results identify a previously unknown mechanism involved in regulation of hematopoietic cell differentiation and in one of the most severe human immunodeficiency syndromes.
网状发育不全是人类严重联合免疫缺陷的一种常染色体隐性形式,其特征为髓系谱系早期分化停滞和淋巴样成熟受损。此外,受影响的新生儿患有双侧感音神经性耳聋。在此,我们在7名患有网状发育不全的个体中鉴定出AK2(腺苷酸激酶2)的双等位基因突变。这些突变导致蛋白质表达缺失或大幅降低。然后我们证明,恢复网状发育不全个体骨髓细胞中的AK2表达可克服中性粒细胞分化停滞,突出了其在一组受限造血谱系发育中的特定需求。最后,我们确定AK2在内耳的血管纹区域特异性表达,这解释了这些个体的感音神经性耳聋。这些结果确定了一种以前未知的参与造血细胞分化调控以及最严重人类免疫缺陷综合征之一的机制。