Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research

We generated three human induced pluripotent stem cell (hiPSC) sublines from human dermal fibroblasts (HDF) (MZT05) generated from a skin biopsy donated from a previously fertile woman. The skin biopsy was broadly consented for generating hiPSC lines for biomedical research, including unique consent...

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Main Authors: Erica C. Pandolfi, Timothy J. Hunt, Sierra Goldsmith, Kellie Hurlbut, Sherman J. Silber, Amander T. Clark
Format: Article
Language:English
Published: Elsevier 2021-07-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506121002555
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author Erica C. Pandolfi
Timothy J. Hunt
Sierra Goldsmith
Kellie Hurlbut
Sherman J. Silber
Amander T. Clark
author_facet Erica C. Pandolfi
Timothy J. Hunt
Sierra Goldsmith
Kellie Hurlbut
Sherman J. Silber
Amander T. Clark
author_sort Erica C. Pandolfi
collection DOAJ
description We generated three human induced pluripotent stem cell (hiPSC) sublines from human dermal fibroblasts (HDF) (MZT05) generated from a skin biopsy donated from a previously fertile woman. The skin biopsy was broadly consented for generating hiPSC lines for biomedical research, including unique consent specifically for studying human fertility, infertility and germ cell differentiation. hiPSCs were reprogrammed using Sendai virus vectors and were subsequently positive for markers of self-renewal. Pluripotency was further verified using PluriTest analysis and in vitro differentiation was tested using Taqman Real-Time PCR assays. These sublines serve as controls for hiPSC research projects aimed at understanding the cell and molecular regulation of female fertility.
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spelling doaj.art-977e1c71a6a94390aaeae5ff705356202022-12-21T22:37:35ZengElsevierStem Cell Research1873-50612021-07-0154102409Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science researchErica C. Pandolfi0Timothy J. Hunt1Sierra Goldsmith2Kellie Hurlbut3Sherman J. Silber4Amander T. Clark5Department of Molecular, Cell and Developmental Biology, Los Angeles, CA 90095, USA; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, CA USA; Molecular Biology Institute, University of California, Los Angeles, CA, USADepartment of Molecular, Cell and Developmental Biology, Los Angeles, CA 90095, USA; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, CA USA; Molecular Biology Institute, University of California, Los Angeles, CA, USAInfertility Center of St. Louis, St. Luke's Hospital, St. Louis, MO, USAInfertility Center of St. Louis, St. Luke's Hospital, St. Louis, MO, USAInfertility Center of St. Louis, St. Luke's Hospital, St. Louis, MO, USADepartment of Molecular, Cell and Developmental Biology, Los Angeles, CA 90095, USA; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, CA USA; Molecular Biology Institute, University of California, Los Angeles, CA, USA; Corresponding author at: Department of Molecular, Cell and Developmental Biology, Los Angeles, CA 90095, USA.We generated three human induced pluripotent stem cell (hiPSC) sublines from human dermal fibroblasts (HDF) (MZT05) generated from a skin biopsy donated from a previously fertile woman. The skin biopsy was broadly consented for generating hiPSC lines for biomedical research, including unique consent specifically for studying human fertility, infertility and germ cell differentiation. hiPSCs were reprogrammed using Sendai virus vectors and were subsequently positive for markers of self-renewal. Pluripotency was further verified using PluriTest analysis and in vitro differentiation was tested using Taqman Real-Time PCR assays. These sublines serve as controls for hiPSC research projects aimed at understanding the cell and molecular regulation of female fertility.http://www.sciencedirect.com/science/article/pii/S1873506121002555
spellingShingle Erica C. Pandolfi
Timothy J. Hunt
Sierra Goldsmith
Kellie Hurlbut
Sherman J. Silber
Amander T. Clark
Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
Stem Cell Research
title Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
title_full Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
title_fullStr Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
title_full_unstemmed Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
title_short Generation of three human induced pluripotent stem cell sublines (UCLAi005-A, UCLAi005-B and UCLAi005-C) for reproductive science research
title_sort generation of three human induced pluripotent stem cell sublines uclai005 a uclai005 b and uclai005 c for reproductive science research
url http://www.sciencedirect.com/science/article/pii/S1873506121002555
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