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诱导多能干细胞(iPSC)资源库,包括来自具有情绪和精神病障碍的遗传隔离家族的临床、基因组和细胞数据。

A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders.

机构信息

Genetic Basis of Mood & Anxiety Disorders Section, Human Genetics Branch, National Institute of Mental Health Intramural Research Program, National Institutes of Health, 35 Convent Drive, Bethesda, MD, 20892, USA.

Laboratorio de Panico e Respiracao, Instituto de Psiquiatria, Universidade Federal do Rio de Janeiro, Rio de Janeiro, 22410-003, Brazil.

出版信息

Transl Psychiatry. 2023 Dec 16;13(1):397. doi: 10.1038/s41398-023-02641-w.

Abstract

Genome-wide (GWAS) and copy number variant (CNV) association studies have reproducibly identified numerous risk alleles associated with bipolar disorder (BD), major depressive disorder (MDD), and schizophrenia (SCZ), but biological characterization of these alleles lags gene discovery, owing to the inaccessibility of live human brain cells and inadequate animal models for human psychiatric conditions. Human-derived induced pluripotent stem cells (iPSCs) provide a renewable cellular reagent that can be differentiated into living, disease-relevant cells and 3D brain organoids carrying the full complement of genetic variants present in the donor germline. Experimental studies of iPSC-derived cells allow functional characterization of risk alleles, establishment of causal relationships between genes and neurobiology, and screening for novel therapeutics. Here we report the creation and availability of an iPSC resource comprising clinical, genomic, and cellular data obtained from genetically isolated families with BD and related conditions. Results from the first 324 study participants, 61 of whom have validated pluripotent clones, show enrichment of rare single nucleotide variants and CNVs overlapping many known risk genes and pathogenic CNVs. This growing iPSC resource is available to scientists pursuing functional genomic studies of BD and related conditions.

摘要

全基因组(GWAS)和拷贝数变异(CNV)关联研究已经重复性地鉴定出许多与双相情感障碍(BD)、重度抑郁症(MDD)和精神分裂症(SCZ)相关的风险等位基因,但由于无法获得活的人脑细胞和用于人类精神疾病的不充分的动物模型,这些等位基因的生物学特征落后于基因发现。人类诱导多能干细胞(iPSC)提供了一种可再生的细胞试剂,可以分化为具有供体种系中存在的全部遗传变异的活的、与疾病相关的细胞和 3D 脑类器官。iPSC 衍生细胞的实验研究允许对风险等位基因进行功能特征分析、在基因和神经生物学之间建立因果关系,并筛选新型治疗方法。在这里,我们报告了一个 iPSC 资源的创建和可用性,该资源包括来自具有 BD 和相关病症的遗传隔离家庭的临床、基因组和细胞数据。来自最初的 324 名研究参与者的结果,其中 61 名参与者的多能克隆已经得到验证,显示出罕见的单核苷酸变异和与许多已知风险基因和致病性 CNV 重叠的 CNV 的富集。这个不断增长的 iPSC 资源可供从事 BD 和相关病症的功能基因组研究的科学家使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06f/10725500/a7fbaabb89e7/41398_2023_2641_Fig1_HTML.jpg

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