Neutrophil generation from hematopoietic progenitor cells and induced pluripotent stem cells (iPSCs): potential applications

被引:5
作者
Jafarzadeh, Abdollah [1 ,2 ,3 ]
Motaghi, Marzieh [4 ]
Patra, Sanand Kumar [5 ]
Jafarzadeh, Zahra [6 ]
Nemati, Maryam [4 ]
Saha, Bhaskar [5 ]
机构
[1] Kerman Univ Med Sci, Appl Cellular & Mol Res Ctr, Kerman, Iran
[2] Kerman Univ Med Sci, Sch Med, Dept Immunol, Pajoohesh Sq, Kerman 7616913555, Iran
[3] Zahedan Univ Med Sci, Clin Immunol Res Ctr, Zahedan, Iran
[4] Kerman Univ Med Sci, Sch Para Med, Dept Hematol & Lab Sci, Kerman, Iran
[5] Natl Ctr Cell Sci, Ganeshkhind, Pune, India
[6] Kerman Univ Med Sci, Student Res Comm, Fac Pharm, Kerman, Iran
关键词
cell differentiation; cellular therapy; hematopoietic progenitor cells; induced pluripotent stem cells; neutrophils; SEVERE CONGENITAL NEUTROPENIA; EX-VIVO EXPANSION; FUNCTIONAL NEUTROPHILS; MATURE NEUTROPHILS; IN-VITRO; G-CSF; DIFFERENTIATION; PATIENT; TRANSPLANTATION; TRANSFUSIONS;
D O I
10.1016/j.jcyt.2024.03.483
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Neutrophils are the most frequent immune cell type in peripheral blood, performing an essential role against pathogens. People with neutrophil deficiencies are susceptible to deadly infections, highlighting the importance of generating these cells in host immunity. Neutrophils can be generated from hematopoietic progenitor cells (HPCs) and embryonic stem cells (ESCs) using a cocktail of cytokines. In addition, induced pluripotent stem cells (iPSCs) can be differentiated into various functional cell types, including neutrophils. iPSCs can be derived from differentiated cells, such as skin and blood cells, by reprogramming them to a pluripotent state. Neutrophil generation from iPSCs involves a multistep process that can be performed through feeder cell-dependent and feeder cell-independent manners. Various cytokines and growth factors, in particular, stem cell facto, IL-3, thrombopoietin and granulocyte colony-stimulating factor (G-CSF), are used in both methods, especially, G-CSF which induces the final differentiation of neutrophils in the granulocyte lineage. iPSC-derived neutrophils have been used as a valuable tool for studying rare genetic disorders affecting neutrophils. The iPSC-derived neutrophils can also be used for disease modeling, infection research and drug discovery. However, several challenges must be overcome before iPSC-derived neutrophils can be used therapeutically in transplantation medicine. This review provides an overview of the commonly employed protocols for generating neutrophils from HPCs, ESCs and iPSCs and discusses the potential applications of the generated cells in research and medicine. (c) 2024 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:797 / 805
页数:9
相关论文
共 76 条
[1]   Neutrophil Function: From Mechanisms to Disease [J].
Amulic, Borko ;
Cazalet, Christel ;
Hayes, Garret L. ;
Metzler, Kathleen D. ;
Zychlinsky, Arturo .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30, 2012, 30 :459-489
[2]   Generation of pluripotent stem cells from adult mouse liver and stomach cells [J].
Aoi, Takashi ;
Yae, Kojiro ;
Nakagawa, Masato ;
Ichisaka, Tomoko ;
Okita, Keisuke ;
Takahashi, Kazutoshi ;
Chiba, Tsutomu ;
Yamanaka, Shinya .
SCIENCE, 2008, 321 (5889) :699-702
[3]   Protection against lethal Aspergillus fumigatus infection in mice by allogeneic myeloid progenitors is not major histocompatibility complex restricted [J].
Arber, C ;
Bitmansour, A ;
Shashidhar, S ;
Wang, S ;
Tseng, B ;
Brown, JMY .
JOURNAL OF INFECTIOUS DISEASES, 2005, 192 (09) :1666-1671
[4]   A method for high-purity isolation of neutrophil granulocytes for functional cell migration assays [J].
Avci, Edibe ;
Akkaya-Ulum, Yeliz Z. ;
Yoyen-Ermis, Digdem ;
Esendagli, Gunes ;
Balci-Peynircioglu, Banu .
TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, 2019, 44 (06) :810-821
[5]   Temporal Analysis of Genome Alterations Induced by Single-Cell Passaging in Human Embryonic Stem Cells [J].
Bai, Qiang ;
Ramirez, Jean-Marie ;
Becker, Fabienne ;
Pantesco, Veronique ;
Lavabre-Bertrand, Thierry ;
Hovatta, Outi ;
Lemaitre, Jean-Marc ;
Pellestor, Franck ;
De Vos, John .
STEM CELLS AND DEVELOPMENT, 2015, 24 (05) :653-662
[6]   Studying Neutrophil Function in vitro: Cell Models and Environmental Factors [J].
Blanter, Marfa ;
Gouwy, Mieke ;
Struyf, Sofie .
JOURNAL OF INFLAMMATION RESEARCH, 2021, 14 :141-162
[7]   Large-scale expansion and transplantation of CD34+ hematopoietic cells: in vitro and in vivo confirmation of neutropenia abrogation related to the expansion process without impairment of the long-term engraftment capacity [J].
Boiron, Jean-Michel ;
Dazey, Bernard ;
Cailliot, Christian ;
Launay, Beatrice ;
Attal, Michel ;
Mazurier, Frederic ;
McNiece, Ian K. ;
Ivanovic, Zoran ;
Caraux, Jean ;
Marit, Gerald ;
Reiffers, Josy .
TRANSFUSION, 2006, 46 (11) :1934-1942
[8]   Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X-0-Linked, AR22(0)- and AR47(0)- Chronic Granulomatous Diseases [J].
Brault, Julie ;
Goutagny, Erwan ;
Telugu, Narasimha ;
Shao, Kaifeng ;
Baquie, Mathurin ;
Satre, Veronique ;
Coutton, Charles ;
Grunwald, Didier ;
Brion, Jean-Paul ;
Barlogis, Vincent ;
Stephan, Jean-Louis ;
Plantaz, Dominique ;
Hescheler, Juergen ;
Krause, Karl-Heinz ;
Saric, Tomo ;
Stasia, Marie Jose .
BIORESEARCH OPEN ACCESS, 2014, 3 (06) :311-326
[9]   Effective and Rapid Generation of Functional Neutrophils from Induced Pluripotent Stem Cells Using ETV2-Modified mRNA [J].
Brok-Volchanskaya, Vera S. ;
Bennin, David A. ;
Suknuntha, Kran ;
Klemm, Lucas C. ;
Huttenlocher, Anna ;
Slukvin, Igor .
STEM CELL REPORTS, 2019, 13 (06) :1099-1110
[10]   CAR-neutrophil mediated delivery of tumor-microenvironment responsive nanodrugs for glioblastoma chemo-immunotherapy [J].
Chang, Yun ;
Cai, Xuechao ;
Syahirah, Ramizah ;
Yao, Yuxing ;
Xu, Yang ;
Jin, Gyuhyung ;
Bhute, Vijesh J. ;
Torregrosa-Allen, Sandra ;
Elzey, Bennett D. ;
Won, You-Yeon ;
Deng, Qing ;
Lian, Xiaojun Lance ;
Wang, Xiaoguang ;
Eniola-Adefeso, Omolola ;
Bao, Xiaoping .
NATURE COMMUNICATIONS, 2023, 14 (01)