2021
DOI: 10.1016/j.htct.2020.01.005
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Generation of hematopoietic stem/progenitor cells with sickle cell mutation from induced pluripotent stem cell in serum-free system

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Cited by 4 publications
(9 citation statements)
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“…Ideally, hNPPCs derived from the hiPSCs represent a better approach to obtaining hNPPCs. Many studies have been conducted to acquire iPSCs-derived nephrogenic progenitors [ 40 ], chondroprogenitors [ 56 ], and hematopoietic progenitor cells [ 57 ] etc. In our previous study, we hypothesized that NPPCs could differentiate from iPSCs [ 58 ] and documented the differentiation protocol of hiPSCs differentiation into hNPCs [ 23 ].…”
Section: Resultsmentioning
confidence: 99%
“…Ideally, hNPPCs derived from the hiPSCs represent a better approach to obtaining hNPPCs. Many studies have been conducted to acquire iPSCs-derived nephrogenic progenitors [ 40 ], chondroprogenitors [ 56 ], and hematopoietic progenitor cells [ 57 ] etc. In our previous study, we hypothesized that NPPCs could differentiate from iPSCs [ 58 ] and documented the differentiation protocol of hiPSCs differentiation into hNPCs [ 23 ].…”
Section: Resultsmentioning
confidence: 99%
“…Paes et al provided a simple and efficient HSC culture method using an inexpensive in-house prepared medium that is both feeder-free and serum-free [ 73 ]. They concluded that the homegrown medium produced more CD34 + CD45 + HSPCs and erythroid colonies than STEMdiff APEL 2 [ 73 ].…”
Section: Introductionmentioning
confidence: 99%
“…Paes et al provided a simple and efficient HSC culture method using an inexpensive in-house prepared medium that is both feeder-free and serum-free [ 73 ]. They concluded that the homegrown medium produced more CD34 + CD45 + HSPCs and erythroid colonies than STEMdiff APEL 2 [ 73 ]. Moreover, Nafria et al provided a detailed procedure to generate CD45 + CD34 + RUNX1C + HSCs from spin EB that mimic intraembryonic aorta-gonad mesonephros hematopoiesis [ 59 , 74 ].…”
Section: Introductionmentioning
confidence: 99%
“…For many diseases, obtaining HSPCs by their mobilization using drugs is impossible due to the pathology of the diseases. Although induced pluripotent stem cells (iPSCs) generated from patients with erythroid diseases serve as a stable source of erythroid cells [10,11], this strategy is tedious and expensive. Furthermore, erythroid cells generated from iPSCs exhibit characteristics of primitive erythrocytes [12,13] with inefficient terminal maturation [14][15][16] and expression of embryonic and fetal stage proteins [13][14][15][16][17].…”
Section: Introductionmentioning
confidence: 99%
“…XY,-10,der(10),add(21)(q22)[20] 16945,XY,-10,der(10),add(21)(q22)[18] PBiEPC-XY,+8,-18,+19,+21[10]/49,XY,+8,del(18)(p11.2),+19,+21[7] 181 44~48,XY,-Y,+8,-18,+19,+21[cp6] CD34iEPC 143 80~87<4n>,XXX,der(X),-3,add(4)(p13),del(4)(q21),der(4;11)(p13;q23),der(5;11)(q35;q23),-7, add(7)(p14), der(8;15)(p23;p10),-9, add(9)(q34),der(10),-12, der(13;15)(p10;p10),-14,-17, i(17)(q10), add(21)(p10), add(21)(q21), +mar[cp20] 157 79~92<4n>,XXX,der(X),-3,add(6)(p23),-7,t(7;10)(q32;q24),add(8)(p27), der(8),-9, -10,-11,-11,-12, der(13), -14,-15,der(15),-16,der(17),i(17)(q10),der(21),+mar,+mar[cp20]…”
mentioning
confidence: 99%