Abstract:
:Primary hepatocyte transplantation (HTx) is a safe cell therapy for patients with liver disease, but wider application is circumvented by poor cell engraftment due to limitations in hepatocyte quality and transplantation strategies. Hepatocyte-like cells (HLCs) derived from human induced pluripotent stem cells (hiPSC) are considered a promising alternative but also require optimisation of transplantation and are often transplanted prior to full maturation. Whole-body in vivo imaging would be highly beneficial to assess engraftment non-invasively and monitor the transplanted cells in the short and long-term. Here we report a lentiviral transduction approach designed to engineer hiPSC-derived HLCs during differentiation. This strategy resulted in the successful production of sodium iodide symporter (NIS)-expressing HLCs that were functionally characterised, transplanted into mice, and subsequently imaged using radionuclide tomography.
journal_name
Stem Cell Resjournal_title
Stem cell researchauthors
Ashmore-Harris C,Blackford SJ,Grimsdell B,Kurtys E,Glatz MC,Rashid TS,Fruhwirth GOdoi
10.1016/j.scr.2019.101599subject
Has Abstractpub_date
2019-12-01 00:00:00pages
101599eissn
1873-5061issn
1876-7753pii
S1873-5061(19)30229-6journal_volume
41pub_type
杂志文章abstract::SOX4 has been shown to promote neuronal differentiation both in the adult and embryonic neural progenitors. Ectopic SOX4 expression has also been shown to inhibit oligodendrocyte differentiation in mice, however the underlying molecular mechanisms remain poorly understood. Here we demonstrate that SOX4 regulates trans...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.10.005
更新日期:2018-12-01 00:00:00
abstract::Osteogenesis Imperfecta (OI) is a rare autosomal dominant metabolic disorder caused by heterozygous mutations in the COL1A1 or COL1A2 genes, which encode the pro-α1(I) and pro-α2(I) chains of type I procollagen, respectively. A human induced pluripotent stem cell (iPSC) line, termed as CHFUi001-A, was generated from p...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101907
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abstract::Reprogramming technology enables the production of neural progenitor cells (NPCs) from somatic cells by direct transdifferentiation. However, little is known on how neural programs in these induced neural stem cells (iNSCs) differ from those of alternative stem cell populations in vitro and in vivo. Here, we performed...
journal_title:Stem cell research
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doi:10.1016/j.scr.2016.04.015
更新日期:2016-05-01 00:00:00
abstract::Rubinstein-Taybi syndrome (RSTS) is a neurodevelopmental disorder characterized by growth retardation, skeletal anomalies and intellectual disability, caused by heterozygous mutations in either CREBBP (RSTS1) or EP300 (RSTS2) genes. We characterized 3 iPSC lines generated by Sendai from blood of RSTS1 patients with un...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101553
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abstract::In order to evaluate the functional significance of palmitoylation during multi-potent neural stem/progenitor cell proliferation and differentiation, retinoic acid-induced P19 cells were used in this study as a model system. Cell behaviour was monitored in the presence of the protein palmitoylation inhibitor 2-bromopa...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2013.12.010
更新日期:2014-03-01 00:00:00
abstract::Mesenchymal stem cells (MSC) have been isolated from almost every adult tissue. In cord blood (CB), different non-hematopoietic CD45-, CD34- adherent cell populations can be generated: the cord blood derived MSC (CB-MSC), that behave almost like MSC from bone marrow (BM-MSC), and unrestricted somatic stem cells (USSC)...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2010.03.004
更新日期:2010-07-01 00:00:00
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journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.10.016
更新日期:2018-12-01 00:00:00
abstract::Induced pluripotent stem (iPS) cells are generated from mouse and human somatic cells by forced expression of defined transcription factors using different methods. Amniotic fluid (AF) cells are easy to obtain from routinely scheduled procedures for prenatal diagnosis and iPS cells have been generated from human AF. H...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2015.09.009
更新日期:2015-11-01 00:00:00
abstract::Pluripotency is a cellular state of multiple options. Here, we highlight the potential for self-organization to contribute to stem cell fate computation. A new way of considering regulatory circuitry is presented that describes the expression of each transcription factor (TF) as a branching process that propagates thr...
journal_title:Stem cell research
pub_type: 杂志文章,评审
doi:10.1016/j.scr.2011.11.001
更新日期:2012-03-01 00:00:00
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journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2014.04.012
更新日期:2014-07-01 00:00:00
abstract:OBJECTIVE:Fecal incontinence reduces the quality of life of many women but has no long-term cure. Research on mesenchymal stem cell (MSC)-based therapies has shown promising results. The primary aim of this study was to evaluate functional recovery after treatment with MSCs in two animal models of anal sphincter injury...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2012.10.002
更新日期:2013-01-01 00:00:00
abstract::Incomplete achromatopsia (ACHM) is a disorder in which there is function defect of cone photoreceptors in the retina and individuals with such disease retain residual color vision. Here, we have generated an induced pluripotent stem cell (iPSC) line carrying a homozygous mutation in the PDE6C gene, already related wit...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101569
更新日期:2019-10-01 00:00:00
abstract::Human embryonic stem cell (hESC) line chHES-478 was derived from abnormal blastocyst diagnosed with albinism after preimplantation genetic diagnosis (PGD) treatment. DNA sequencing analysis confirmed that chHES-478 cell line carried a compound heterozygous mutation, c.896G>A(p.Arg299His) and c.929_930insC(p.Pro310Glnf...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.11.004
更新日期:2016-11-01 00:00:00
abstract::Maintenance of hematopoietic stem cells and their potential to give rise to progenitors of differentiated lymphoid and myeloid cells are accomplished by a network of regulatory processes. As a part of this network, the heteromeric transcription factor GA-binding protein (GABP) plays a crucial role in self-renewal of m...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.04.007
更新日期:2016-05-01 00:00:00
abstract::Insulin-like growth factor 1 (IGF-1) plays an important role in the regulation of tooth root development, and stem cells from apical papilla (SCAPs) are responsible for the formation of root pulp and dentin. To date, it remains unclear whether IGF-1 can regulate the function of SCAPs. In this study, SCAPs were isolate...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2011.12.005
更新日期:2012-05-01 00:00:00
abstract::The human embryonic stem cell line RCe011-A (RC-7) was derived from a failed to fertilise oocyte voluntarily donated as unsuitable and surplus to fertility requirements following ethics committee approved informed consent under licence from the UK Human Fertilisation and Embryology Authority. The cell line shows norma...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.02.036
更新日期:2016-03-01 00:00:00
abstract::Human teratoma is a germ cell tumor that contains normal tissues (e.g., hair, skin or cartilage) differentiated from embryonal germ layers. Because of the feature of this tumor, we hypothesized that human teratomas contain multipotent stem cells that can develop into various non-cancerous normal tissues. In this study...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101633
更新日期:2019-12-01 00:00:00
abstract::Maple syrup urine disease type Ib (MSUD Ib) is an autosomal recessive genetic metabolic disease caused by homozygous or compound heterozygous mutation in BCKDHB on chromosome 6q14. We generated an induced pluripotent stem cell (iPSC) line from peripheral blood mononuclear cells (PBMCs) of a 5-day-old boy with MSUD Ib ...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101579
更新日期:2019-10-01 00:00:00
abstract::Bone marrow stromal cell (BMSC) adhesion and migration are fundamental to a number of pathophysiologic processes, including fracture and wound healing. Vitamin C is beneficial for bone formation, fracture repair and wound healing. However, the role of the vitamin C transporter in BMSC adhesion, migration and wound hea...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2013.11.002
更新日期:2014-03-01 00:00:00
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journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2019.101430
更新日期:2019-05-01 00:00:00
abstract::A skin biopsy was obtained from a 14-year-old female patient with a history of Myelomeningocele. Dermal fibroblasts were isolated and reprogrammed with Sendai virus (SeV) vectors encoding OCT3/4, SOX2, KLF4, and c-MYC. The generated induced Pluripotent Stem Cell (iPSC) clones NTDi4_09A were free of genomically integra...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.05.007
更新日期:2018-08-01 00:00:00
abstract::X-linked Alport syndrome (XLAS) is a rare form of hereditary nephritis caused by mutations in the COL4A5 gene encoding the type IV collagen α5 chain. A skin biopsy was performed on one female patient with XLAS who carried a heterozygous p.G409S (c. 1225 G > A) mutation in the COL4A5 gene. A human-induced pluripotent s...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101833
更新日期:2020-05-01 00:00:00
abstract::As one of the most essential genome guardians, p53 and its mutants have been suggested associated with many types of cancers. Many p53 mutants function induce unique phenotypes, including carcinogenesis, metastasis, and drug resistance. The p53(R249S) mutation is the most prevalent and specific mutation associated wit...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.101360
更新日期:2019-01-01 00:00:00
abstract::Autosomal recessive Stargardt disease is the most common cause of inherited retinal disease. In this report, we describe the generation and characterization of two human induced pluripotent stem cell (iPSC) lines from a patient with compound heterozygous mutations in the ABCA4 gene (c.[768G>T];[6079C>T]). Patient derm...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101947
更新日期:2020-10-01 00:00:00
abstract::Two iPSC clones, NCCSi008-A and NCCSi008-B, were generated from a healthy male individual of Indian origin by reprogramming his CD4+ T cells with an integration free Sendai viral vector. The established iPSC clones showed high alkaline phosphatase (ALP) activity, expression of pluripotency markers, a normal male karyo...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.101765
更新日期:2020-05-01 00:00:00
abstract::The peptide hormone insulin produced by pancreatic β-cells undergoes post-transcriptional processing before secretion. In particular, C-peptide is cleaved from pro-insulin to generate mature insulin. Here, we introduce a C-peptide-mCherry human iPSC line (HMGUi001-A-8). The line was generated by CRISPR/Cas9 mediated h...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102126
更新日期:2020-12-16 00:00:00
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journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2020.102120
更新日期:2020-12-10 00:00:00
abstract::The CR-4 human embryonic stem cell line was derived from the inner cell mass of a developing blastocyst. This cell line has been adapted to grow in feeder-free conditions and is especially well-suited for differentiation to retinal pigment epithelium. The line demonstrates a normal human 46,XX female karyotype. Plurip...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2016.12.005
更新日期:2017-01-01 00:00:00
abstract::Leucine rich repeat kinase (LRRK2) is the most prevalent genetic cause for Parkinson's disease. LRRK2 p.G2385R is an Asian specific genetic risk factor for sporadic Parkinson's disease. We generated two induced pluripotent stem cells (iPSCs), IBMS-iPSC-018-09 and IBMS-iPSC-020-01, from the peripheral blood mononuclear...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.01.034
更新日期:2018-04-01 00:00:00
abstract::We describe the generation and characterization of 5 human induced pluripotent stem cell (iPSC) lines derived from peripheral blood mononuclear cells (PBMCs) of healthy adult individuals. The PBMCs were reprogrammed using non-integrating Sendai viruses containing the reprogramming factors POU5F1 (OCT4), SOX2, KLF4 and...
journal_title:Stem cell research
pub_type: 杂志文章
doi:10.1016/j.scr.2018.101380
更新日期:2019-01-01 00:00:00