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升高的 DSCAM 引起的内皮细胞骨硬化蛋白增加介导多种 21 三体表型。

Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypes.

机构信息

Department of Genetics, Harvard Medical School, Boston, Massachusetts, USA.

Cardiovascular Division, Brigham and Women's Hospital, Boston, Massachusetts, USA.

出版信息

J Clin Invest. 2024 Jun 3;134(11):e167811. doi: 10.1172/JCI167811.

Abstract

Trisomy 21 (T21), a recurrent aneuploidy occurring in 1:800 births, predisposes to congenital heart disease (CHD) and multiple extracardiac phenotypes. Despite a definitive genetic etiology, the mechanisms by which T21 perturbs development and homeostasis remain poorly understood. We compared the transcriptome of CHD tissues from 49 patients with T21 and 226 with euploid CHD (eCHD). We resolved cell lineages that misexpressed T21 transcripts by cardiac single-nucleus RNA sequencing and RNA in situ hybridization. Compared with eCHD samples, T21 samples had increased chr21 gene expression; 11-fold-greater levels (P = 1.2 × 10-8) of SOST (chr17), encoding the Wnt inhibitor sclerostin; and 1.4-fold-higher levels (P = 8.7 × 10-8) of the SOST transcriptional activator ZNF467 (chr7). Euploid and T21 cardiac endothelial cells coexpressed SOST and ZNF467; however, T21 endothelial cells expressed 6.9-fold more SOST than euploid endothelial cells (P = 2.7 × 10-27). Wnt pathway genes were downregulated in T21 endothelial cells. Expression of DSCAM, residing within the chr21 CHD critical region, correlated with SOST (P = 1.9 × 10-5) and ZNF467 (P = 2.9 × 10-4). Deletion of DSCAM from T21 endothelial cells derived from human induced pluripotent stem cells diminished sclerostin secretion. As Wnt signaling is critical for atrioventricular canal formation, bone health, and pulmonary vascular homeostasis, we concluded that T21-mediated increased sclerostin levels would inappropriately inhibit Wnt activities and promote Down syndrome phenotypes. These findings imply therapeutic potential for anti-sclerostin antibodies in T21.

摘要

21 三体(T21)是一种在 800 次出生中发生的复发性非整倍体,易患先天性心脏病(CHD)和多种心脏外表型。尽管具有明确的遗传病因,但 T21 扰乱发育和体内平衡的机制仍知之甚少。我们比较了 49 例 T21 合并 CHD (CHD)和 226 例染色体正常的 CHD (eCHD)患者的 CHD 组织的转录组。我们通过心脏单核 RNA 测序和 RNA 原位杂交解析了表达 T21 转录本的细胞谱系。与 eCHD 样本相比,T21 样本的 chr21 基因表达增加;SOST(chr17)的表达水平增加了 11 倍(P = 1.2×10-8),编码 Wnt 抑制剂骨硬化蛋白;SOST 转录激活剂 ZNF467(chr7)的表达水平增加了 1.4 倍(P = 8.7×10-8)。eCHD 和 T21 心脏内皮细胞共同表达 SOST 和 ZNF467;然而,T21 内皮细胞表达的 SOST 比 eCHD 内皮细胞多 6.9 倍(P = 2.7×10-27)。Wnt 通路基因在 T21 内皮细胞中下调。位于 chr21 CHD 关键区域内的 DSCAM 的表达与 SOST(P = 1.9×10-5)和 ZNF467(P = 2.9×10-4)相关。从 T21 诱导多能干细胞衍生的内皮细胞中删除 DSCAM 可减少骨硬化蛋白的分泌。由于 Wnt 信号对于房室管形成、骨骼健康和肺血管内稳态至关重要,我们得出结论,T21 介导的骨硬化蛋白水平升高会不适当抑制 Wnt 活性并促进唐氏综合征表型。这些发现意味着在 T21 中使用抗骨硬化蛋白抗体具有治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d1/11142749/3a5641a9a6c8/jci-134-167811-g120.jpg

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