Repair of acute liver damage with immune evasive hESC derived hepato-blasts.

Abstract:

:Human embryonic stem cells (hESCs) can undergo unlimited self-renewal and differentiate into hepatic cells, including expandable hepato-blasts (HBs) and hepatocyte-like cells (HLCs) in vitro. Therefore, hESC-derived HBs have the potential to become a renewable cell source for cell therapy of serious liver damage. However, one of the key challenges for such cell therapy is the allogeneic immune rejection of hESC-derived HBs. To overcome this challenge, we developed a strategy to protect the hESC-derived HBs from allogeneic immune rejection by ectopically expressing immune suppressive molecules CTLA4-Ig and PD-L1, denoted CP HBs. Like HBs derived from normal hESCs, CP HBs are capable of repairing liver damage in animal models. Using humanized mice (Hu-mice) reconstituted with human immune system, we showed that CP HBs are protected from allogeneic immune system and can survive long-term in Hu-mice. These data support the feasibility to develop CP HBs into a cell therapy to treat serious liver damage.

journal_name

Stem Cell Res

journal_title

Stem cell research

authors

Liu J,Pan T,Chen Y,Liu Y,Yang F,Chen Q,Abbas N,Zhong M,Zhang Q,Xu Y,Li YX

doi

10.1016/j.scr.2020.102010

subject

Has Abstract

pub_date

2020-12-01 00:00:00

pages

102010

eissn

1873-5061

issn

1876-7753

pii

S1873-5061(20)30311-1

journal_volume

49

pub_type

杂志文章
  • Generation of hiPSC line TCIERi001-A from normal human epidermal keratinocytes.

    abstract::Human induced pluripotent stem cell (hiPSC) line TCIERi001-A was generated from normal human epidermal keratinocytes (NHEK) primary cell line with the nonintegrating system using Sendai reprogramming kit. Sendai particles were used to deliver the defined transcription factors that included three vector preparations, s...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2019.101590

    authors: Shrestha R,Wen YT,Tsai RK

    更新日期:2019-12-01 00:00:00

  • Human embryonic stem cells and derived contractile embryoid bodies are susceptible to Coxsakievirus B infection and respond to interferon Iβ treatment.

    abstract::We studied the susceptibility of human embryonic stem cells and derived contractile embryoid bodies from WAO9, HUES-5 and HUES-16 cell lines to Coxsackievirus B infection. After validating stem cell-like properties and cardiac phenotype, Coxsackievirus B receptors CAR and DAF, as well as type I interferon receptors we...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2010.09.002

    authors: Scassa ME,Jaquenod de Giusti C,Questa M,Pretre G,Richardson GA,Bluguermann C,Romorini L,Ferrer MF,Sevlever GE,Miriuka SG,Gómez RM

    更新日期:2011-01-01 00:00:00

  • Generation of induced pluripotent stem cell line (ZZUi004-A) from urine sample of a patient with spinocerebellar ataxia type 3.

    abstract::Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disease caused by a CAG repeat expansion in the region of the ATXN3 gene. The main feature of SCA3 is progressive ataxia, which affects balance, gait, and speech. Urine cells (UCs) of a SCA3 patient were successfully translated to induced...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2018.01.027

    authors: Wang Y,Shi C,Wang Z,Sun H,Yang Z,Zhang F,Liu Y,Liu H,Jiang C,Zhang S,Xu Y,Wen X

    更新日期:2018-04-01 00:00:00

  • Stem cell passage affects directional migration of stem cells in electrotaxis.

    abstract::Stem cells can differentiate into various body tissues and organs and thus are considered as promising tools for cell therapy and tissue engineering. Early passage stem cells have high differentiation ability compared to late passage stem cells. Thus, it is important to use early passage stem cells in cell therapy. He...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2019.101475

    authors: Hong SH,Lee MH,Koo MA,Seon GM,Park YJ,Kim D,Park JC

    更新日期:2019-07-01 00:00:00

  • Constitutive transgene expression of Stem Cell Antigen-1 in the hair follicle alters the sensitivity to tumor formation and progression.

    abstract::The cell surface protein Stem Cell Antigen-1 (Sca-1) marks stem or progenitor cells in several murine tissues and is normally upregulated during cancer development. Although the specific function of Sca-1 remains unknown, Sca-1 seems to play a role in proliferation, differentiation and cell migration in a number of ti...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2017.07.002

    authors: Christensen R,Owens DM,Füchtbauer AC,Gunnarsson A,Ramsing M,Füchtbauer EM,Jensen UB

    更新日期:2017-08-01 00:00:00

  • Generation of a human induced pluripotent stem cell line from urinary cells of a patient with primary congenital glaucoma using integration free Sendai technology.

    abstract::We have generated a human induced pluripotent stem cell (iPSC) line derived from urinary cells of a 10years old patient with primary congenital glaucoma (PCG). The cells were reprogrammed with the human OSKM transcription factors using the Sendai-virus delivery system and shown to have full differentiation potential. ...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2018.04.004

    authors: Zhang J,Wu S,Hu M,Liu Q

    更新日期:2018-05-01 00:00:00

  • Eltrombopag, a thrombopoietin receptor agonist, enhances human umbilical cord blood hematopoietic stem/primitive progenitor cell expansion and promotes multi-lineage hematopoiesis.

    abstract::Umbilical cord blood (UCB) transplantation has emerged as a promising therapy, but it is challenged by scarcity of stem cells. Eltrombopag is a non-peptide, thrombopoietin (TPO) receptor agonist, which selectively activates c-Mpl in humans and chimpanzees. We investigated eltrombopag's effects on human UCB hematopoiet...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2012.05.001

    authors: Sun H,Tsai Y,Nowak I,Liesveld J,Chen Y

    更新日期:2012-09-01 00:00:00

  • Long-term microcarrier suspension cultures of human embryonic stem cells.

    abstract::The conventional method of culturing human embryonic stem cells (hESC) is on two-dimensional (2D) surfaces, which is not amenable for scale up to therapeutic quantities in bioreactors. We have developed a facile and robust method for maintaining undifferentiated hESC in three-dimensional (3D) suspension cultures on ma...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2009.02.005

    authors: Oh SK,Chen AK,Mok Y,Chen X,Lim UM,Chin A,Choo AB,Reuveny S

    更新日期:2009-05-01 00:00:00

  • Intra-subject variability in human bone marrow stromal cell (BMSC) replicative senescence: molecular changes associated with BMSC senescence.

    abstract::The outcomes of clinical trials using bone marrow stromal cell (BMSC) are variable; the degree of the expansion of BMSCs during clinical manufacturing may contribute to this variability since cell expansion is limited by senescence. Human BMSCs from aspirates of healthy subjects were subcultured serially until cell gr...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2013.07.005

    authors: Ren J,Stroncek DF,Zhao Y,Jin P,Castiello L,Civini S,Wang H,Feng J,Tran K,Kuznetsov SA,Robey PG,Sabatino M

    更新日期:2013-11-01 00:00:00

  • Adrenomedullin promotes differentiation of oligodendrocyte precursor cells into myelin-basic-protein expressing oligodendrocytes under pathological conditions in vitro.

    abstract::Oligodendrocytes, which are the main cell type in cerebral white matter, are generated from their precursor cells (oligodendrocyte precursor cells: OPCs). However, the differentiation from OPCs to oligodendrocytes is disturbed under stressed conditions. Therefore, drugs that can improve oligodendrocyte regeneration ma...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2015.05.001

    authors: Maki T,Takahashi Y,Miyamoto N,Liang AC,Ihara M,Lo EH,Arai K

    更新日期:2015-07-01 00:00:00

  • Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant.

    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

    authors: Cheng YC,Huang CY,Ho MC,Hsu YH,Syu SH,Lu HE,Lin HI,Lin CH,Hsieh PCH

    更新日期:2018-04-01 00:00:00

  • Generation of two induced pluripotent stem cell lines from a patient with Stargardt Macular Dystrophy caused by the c.768G>T and c.6079C>T mutations in ABCA4.

    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

    authors: Jennings L,Zhang D,Chen SC,Moon SY,Lamey T,Thompson JA,McLaren T,De Roach JN,Chen FK,McLenachan S

    更新日期:2020-10-01 00:00:00

  • Generation of non-transgenic iPS cells from human cord blood CD34+ cells under animal component-free conditions.

    abstract::Recently, many hurdles and limitations for production of clinically applicable iPSC derivatives have been overcome. Transgene-free iPSCs can be efficiently derived from easily accessible cell sources such as blood. Here we describe the generation of transgene-free hiPS cells from cord blood derived CD34+ cells, reprog...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2017.03.022

    authors: Haase A,Göhring G,Martin U

    更新日期:2017-05-01 00:00:00

  • Establishment of TUSMi007-A, an induced pluripotent stem cell (iPSC) line from an 83-year old Chinese Han patient with Alzheimer's disease (AD).

    abstract::An 83-year old Alzheimer's disease (AD) male patient donated his Peripheral blood mononuclear cells (PBMC). The non-integrating episomal vector system used to reprogram PBMCs with the human OKSM transcription factors. The pluripotency of transgene-free iPSCs was confirmed by immunocytochemistry for pluripotency marker...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2018.11.008

    authors: Wang Y,Zhang J,Lei Y,Zhao J

    更新日期:2018-12-01 00:00:00

  • Derivation and characterization of the human embryonic stem cell line CR-4: Differentiation to human retinal pigment epithelial cells.

    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

    authors: Mazzilli JL,Domozhirov AY,Mueller-Ortiz SL,Garcia CA,Wetsel RA,Zsigmond EM

    更新日期:2017-01-01 00:00:00

  • Laminin α5 substrates promote survival, network formation and functional development of human pluripotent stem cell-derived neurons in vitro.

    abstract::Laminins are one of the major protein groups in the extracellular matrix (ECM) and specific laminin isoforms are crucial for neuronal functions in the central nervous system in vivo. In the present study, we compared recombinant human laminin isoforms (LN211, LN332, LN411, LN511, and LN521) and laminin isoform fragmen...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2017.09.002

    authors: Hyysalo A,Ristola M,Mäkinen ME,Häyrynen S,Nykter M,Narkilahti S

    更新日期:2017-10-01 00:00:00

  • Pluripotent stem cell-derived interneuron progenitors mature and restore memory deficits but do not suppress seizures in the epileptic mouse brain.

    abstract::GABAergic interneuron dysfunction has been implicated in temporal lobe epilepsy (TLE), autism, and schizophrenia. Inhibitory interneuron progenitors transplanted into the hippocampus of rodents with TLE provide varying degrees of seizure suppression. We investigated whether human embryonic stem cell (hESC)-derived int...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2018.10.007

    authors: Anderson NC,Van Zandt MA,Shrestha S,Lawrence DB,Gupta J,Chen CY,Harrsch FA,Boyi T,Dundes CE,Aaron G,Naegele JR,Grabel L

    更新日期:2018-12-01 00:00:00

  • Derivation of NEM2 affected human embryonic stem cell line Genea079.

    abstract::The Genea079 human embryonic stem cell line was derived from a donated, fully commercially consented ART blastocyst, carrying compound heterozygous mutations in the NEB gene, exon 55 deletion & c.15110dupA, indicative of Nemaline Myopathy Type 2 (NEM2). Following ICM outgrowth on inactivated human feeders, karyotype w...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2016.02.015

    authors: Dumevska B,McKernan R,Goel D,Schmidt U

    更新日期:2016-03-01 00:00:00

  • Derivation, characterization, and gene expression profile of two new human ES cell lines from India.

    abstract::Human embryonic stem cells (hESCs) offer new avenues for studying human development and disease progression in addition to their tremendous potential toward development of cell-replacement therapies for various cellular disorders. We have earlier reported the derivation and characterization of Relicell(®) hES1, the fi...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2010.07.001

    authors: Mandal A,Bhowmik S,Patki A,Viswanathan C,Majumdar AS

    更新日期:2010-11-01 00:00:00

  • Genomic imprinting is variably lost during reprogramming of mouse iPS cells.

    abstract::Derivation of induced pluripotent stem (iPS) cells is mainly an epigenetic reprogramming process. It is still quite controversial how genomic imprinting is reprogrammed in iPS cells. Thus, we derived multiple iPS clones from genetically identical mouse somatic cells. We found that parentally inherited imprint was vari...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2013.05.011

    authors: Takikawa S,Ray C,Wang X,Shamis Y,Wu TY,Li X

    更新日期:2013-09-01 00:00:00

  • Generation of OCT4-EGFP, NANOG-tdTomato dual reporter human induced pluripotent stem cell line, KKUi001-A, using the CRISPR/Cas9 system.

    abstract::OCT4 and NANOG are core transcription factor genes in self-renewal, differentiation, and reprogramming. Here, we generated an OCT4-EGFP, NANOG-tdTomato dual reporter hiPSC line, KKUi001-A, on the basis of human induced pluripotent stem cells using CRISPR/Cas9 technology. EGFP and tdTomato reporter were inserted into b...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2020.101943

    authors: Lee M,Choi NY,Park S,Bang JS,Lee Y,Jeong D,Ham S,Lim S,Kim KH,Ko K

    更新日期:2020-10-01 00:00:00

  • Generation of a gene corrected human isogenic IBMS-iPSC-014-C from polycystic-kidney-disease induced pluripotent stem cell line using CRISPR/Cas9.

    abstract::We report the engendering an isogenic iPSC line from the IBMS-iPSC-014-05 with homozygous correction of the R803X, Chr4: 88989098C > T in PKD2, using CRISPR/Cas9 technology. The results from the isogenic control, IBMS-iPSC-014-05C, showed that mutation had been corrected, while maintaining normal morphology, pluripote...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2020.101784

    authors: Liu CL,Huang CY,Chen HC,Lu HE,Hsieh PCH,Lee JJ

    更新日期:2020-05-01 00:00:00

  • Generation of two control iPSC clones NCCSi008-A and NCCSi008-B from an individual of Indian ethnicity.

    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

    authors: Vaidyanath A,Khan M,Shiras A

    更新日期:2020-05-01 00:00:00

  • Generation of a transgene-free induced pluripotent stem cells line (UNIPDi002-A) from oral mucosa epithelial stem cells carrying the R304Q mutation in TP63 gene.

    abstract::Transgene free UNIPDi002-A-human induced pluripotent stem cell (hiPSC) line was generated by Sendai Virus Vectors reprogramming from human oral mucosal epithelial stem cells (hOMESCs) of a patient affected by ectrodactyly-ectodermal dysplasia-clefting (EEC)-syndrome, carrying a mutation in exon 8 of the TP63 gene (R30...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2018.02.006

    authors: Trevisan M,Barbaro V,Riccetti S,Masi G,Barzon L,Nespeca P,Alvisi G,Di Iorio E,Palù G

    更新日期:2018-04-01 00:00:00

  • Generation of induced pluripotent stem cells (iPSCs) from a hereditary spastic paraplegia patient carrying a homozygous Y275X mutation in CYP7B1 (SPG5).

    abstract::Skin fibroblasts were obtained from a 47-year-old hereditary spastic paraplegia patient carrying a homozygous mutation Y275X in CYP7B1 (Cytochrome P450, Family 7, Subfamily B, Polypeptide 1), responsible for causing hereditary spastic paraplegia type 5 (SPG5). Induced pluripotent stem cells (iPSCs) were generated by t...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2016.09.011

    authors: Hauser S,Höflinger P,Theurer Y,Rattay TW,Schöls L

    更新日期:2016-09-01 00:00:00

  • Predictive bioinformatics identifies novel regulators of proliferation in a cancer stem cell model.

    abstract::The cancer stem cell model postulates that tumors are hierarchically organized with a minor population, the cancer stem cells, exhibiting unlimited proliferative potential. These cells give rise to the bulk of tumor cells, which retain a limited ability to divide. Without successful targeting of cancer stem cells, tum...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2017.11.009

    authors: Fields E,Wren JD,Georgescu C,Daum JR,Gorbsky GJ

    更新日期:2018-01-01 00:00:00

  • Establishment of human embryonic stem cell WAe009-A-48 carrying a long QT syndrome mutation in SCN5A.

    abstract::The long QT syndrome type 3 (LQT3) is currently the 3rd most prevalent of the 15 known types of LQT syndrome. Cardiac events in LQT3 are less frequent than LQT1 and LQT2, but more likely to be fatal. LQT3 is caused by mutation in gene SCN5A, which codes for the Nav1.5 Na+ channel. Herein, we have generated a human emb...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2021.102194

    authors: Yang X,Wu F,Zhong J,Li F

    更新日期:2021-01-25 00:00:00

  • Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene.

    abstract::Frontotemporal dementia with parkinsonism linked to chromosome 17q21.2 (FTDP-17) is an autosomal-dominant neurodegenerative disorder. Mutations in the MAPT (microtubule-associated protein tau) gene can cause FTDP-17, but the underlying pathomechanisms of the disease are still unknown. Induced pluripotent stem cells (i...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2016.09.024

    authors: Nimsanor N,Poulsen U,Rasmussen MA,Clausen C,Mau-Holzmann UA,Nielsen JE,Nielsen TT,Hyttel P,Holst B,Schmid B

    更新日期:2016-11-01 00:00:00

  • The Sirt1 activator SRT3025 expands hematopoietic stem and progenitor cells and improves hematopoiesis in Fanconi anemia mice.

    abstract::Fanconi anemia is a genetic bone marrow failure syndrome. The current treatment options are suboptimal and do not prevent the eventual onset of aplastic anemia requiring bone marrow transplantation. We previously showed that resveratrol, an antioxidant and an activator of the protein deacetylase Sirt1, enhanced hemato...

    journal_title:Stem cell research

    pub_type: 杂志文章

    doi:10.1016/j.scr.2015.05.007

    authors: Zhang QS,Deater M,Schubert K,Marquez-Loza L,Pelz C,Sinclair DA,Grompe M

    更新日期:2015-07-01 00:00:00

  • Generation of an induced pluripotent stem cell line (CHFUi001-A) from an osteogenesis imperfecta patient with COL1A2 mutation.

    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

    authors: Zheng Z,Lu W,Pei Z,Chen J,Yang T,Luo F

    更新日期:2020-07-05 00:00:00