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A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals

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TLDR
A gender-balanced, racially/ethnically diverse library of human induced pluripotent stem cells (hiPSC) lines from 40 clinically healthy human individuals who range in age from 22 to 61 years was reported in this article.
Abstract
Summary A library of well-characterized human induced pluripotent stem cell (hiPSC) lines from clinically healthy human subjects could serve as a useful resource of normal controls for in vitro human development, disease modeling, genotype-phenotype association studies, and drug response evaluation. We report generation and extensive characterization of a gender-balanced, racially/ethnically diverse library of hiPSC lines from 40 clinically healthy human individuals who range in age from 22 to 61 years. The hiPSCs match the karyotype and short tandem repeat identities of their parental fibroblasts, and have a transcription profile characteristic of pluripotent stem cells. We provide whole-genome sequencing data for one hiPSC clone from each individual, genomic ancestry determination, and analysis of mendelian disease genes and risks. We document similar transcriptomic profiles, single-cell RNA-sequencing-derived cell clusters, and physiology of cardiomyocytes differentiated from multiple independent hiPSC lines. This extensive characterization makes this hiPSC library a valuable resource for many studies on human biology.

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Citations
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Functional Effects of Cardiomyocyte Injury in COVID-19

- 26 Jan 2022 - 
TL;DR: In this article , the authors integrated cell biological and physiological analyses of human cardiomyocytes differentiated from human induced pluripotent stem cells (hiPSCs) infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the presence of interleukins (ILs) with clinical findings related to laboratory values in COVID-19 patients.
Journal ArticleDOI

Fibroblast growth factor homologous factors serve as a molecular rheostat in tuning arrhythmogenic cardiac late sodium current

TL;DR: In this article , the authors demonstrate that the intracellular fibroblast growth factor homologous factors (FHF1−4) tune pathogenic late sodium current (INa,L) in an isoform-specific manner.
Journal ArticleDOI

Action potential variability in human pluripotent stem cell-derived cardiomyocytes obtained from healthy donors

TL;DR: In this article , the authors report the action potential variability of 780 cardiomyocytes derived from pluripotent stem cells obtained from six healthy donors and conclude that even using the same cell line and differentiation protocol, the differentiation batch still affects the results.
Journal ArticleDOI

Harshening stem cell research and precision medicine: The states of human pluripotent cells stem cell repository diversity, and racial and sex differences in transcriptomes

TL;DR: This paper analyzed the diversity of human induced pluripotent stem cells with respect to ethnicity, sex, and disease types, and revealed a lack of diversity despite the large sample size of human ILP cells and showed that the White group made up the majority of the banked ILP stem cells.
References
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Journal ArticleDOI

Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined Factors

TL;DR: It is demonstrated that iPS cells can be generated from adult human fibroblasts with the same four factors: Oct3/4, Sox2, Klf4, and c-Myc.
Journal ArticleDOI

Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

TL;DR: This article showed that OCT4, SOX2, NANOG, and LIN28 factors are sufficient to reprogram human somatic cells to pluripotent stem cells that exhibit the essential characteristics of embryonic stem (ES) cells.
Journal ArticleDOI

Reprogramming of human somatic cells to pluripotency with defined factors

TL;DR: The data demonstrate that defined factors can reprogramme human cells to pluripotency, and establish a method whereby patient-specific cells might be established in culture.
Journal ArticleDOI

ClinVar: public archive of relationships among sequence variation and human phenotype

TL;DR: To facilitate evaluation of the medical importance of each variant, ClinVar aggregates submissions with the same variation/phenotype combination, adds value from other NCBI databases, assigns a distinct accession of the format RCV000000000.0 and reports if there are conflicting clinical interpretations.
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How can Eliza be used for stem cell research?

The provided paper does not mention anything about Eliza or its use in stem cell research.