Two decades of embryonic stem cells: a historical overview

被引:42
|
作者
Eguizabal, C. [1 ]
Aran, B. [2 ]
Lopes, S. M. Chuva de Sousa [3 ,4 ]
Geens, M. [5 ]
Heindryckx, B. [4 ]
Panula, S. [6 ]
Popovic, M. [4 ]
Vassena, R. [7 ]
Veiga, A. [2 ,8 ]
机构
[1] Basque Ctr Blood Transfus & Human Tissues, Cell Therapy & Stem Cell Grp, Barrio Labeaga S-N, Galdakao 48960, Spain
[2] Ctr Regenerat Med Barcelona, Barcelona Stem Cell Bank, Barcelona 08908, Spain
[3] Leiden Univ Med Ctr, Dept Anat & Embryol, Einthovenweg 20, NL-2333 ZC Leiden, Netherlands
[4] Ghent Univ Hosp, Dept Reprod Med, Ghent Fertil & Stem Cell Team G FaST, B-9000 Ghent, Belgium
[5] Vrije Univ Brussel, Res Grp Reprod & Genet, Laarbeeklaan 103, B-1090 Brussels, Belgium
[6] Karolinska Inst, Dept Clin Sci Intervent & Technol, S-17177 Stockholm, Sweden
[7] Clin EUGIN, Barcelona 08029, Spain
[8] Hosp Univ Dexeus, Dexeus Mujer, Barcelona 08028, Spain
基金
欧洲研究理事会;
关键词
pluripotency; human embryonic stem cell (hESC); human-induced pluripotent stem cells (hiPSC); regenerative medicine; differentiation; clinical trials; PRIMORDIAL GERM-CELLS; X-CHROMOSOME INACTIVATION; GENOME-EDITING SYSTEM; LONG QT SYNDROME; NUCLEAR TRANSFER; IN-VITRO; SELF-RENEWAL; HOMOLOGOUS RECOMBINATION; GENETIC CORRECTION; DIRECTED DIFFERENTIATION;
D O I
10.1093/hropen/hoy024
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
STUDY QUESTION: How did the field of stem cell research develop in the years following the derivation of the first human embryonic stem cell (hESC) line? SUMMARY ANSWER: Supported by the increasing number of clinical trials to date, significant technological advances in the past two decades have brought us ever closer to clinical therapies derived from pluripotent cells. WHAT IS KNOWN ALREADY: Since their discovery 20 years ago, the use of human pluripotent stem cells has progressed tremendously from bench to bedside. Here, we provide a concise review of the main keystones of this journey and focus on ongoing clinical trials, while indicating the most relevant future research directions. STUDY DESIGN, SIZE, DURATION: This is a historical narrative, including relevant publications in the field of pluripotent stem cells (PSC) derivation and differentiation, recounted both through scholarly research of published evidence and interviews of six pioneers who participated in some of the most relevant discoveries in the field. PARTICIPANTS/MATERIALS, SETTING, METHODS: The authors all contributed by researching the literature and agreed upon body of works. Portions of the interviews of the field pioneers have been integrated into the review and have also been included in full for advanced reader interest. MAIN RESULTS AND THE ROLE OF CHANCE: The stem cell field is ever expanding. We find that in the 20 years since the derivation of the first hESC lines, several relevant developments have shaped the pluripotent cell field, from the discovery of different states of pluripotency, the derivation of induced PSC, the refinement of differentiation protocols with several clinical trials underway, as well as the recent development of organoids. The challenge for the years to come will be to validate and refine PSCs for clinical use, from the production of highly defined cell populations in clinical grade conditions to the possibility of creating replacement organoids for functional, if not anatomical, function restoration. LIMITATIONS, REASONS FOR CAUTION: This is a non-systematic review of current literature. Some references may have escaped the experts' analysis due to the exceedingly diverse nature of the field. As the field of regenerative medicine is rapidly advancing, some of the most recent developments may have not been captured entirely. WIDER IMPLICATIONS OF THE FINDINGS: The multi-disciplinary nature and tremendous potential of the stem cell field has important implications for basic as well as translational research. Recounting these activities will serve to provide an in-depth overview of the field, fostering a further understanding of human stem cell and developmental biology. The comprehensive overview of clinical trials and expert opinions included in this narrative may serve as a valuable scientific resource, supporting future efforts in translational approaches. STUDY FUNDING/COMPETING INTEREST(S): ESHRE provided funding for the authors' on-site meeting and discussion during the preparation of this manuscript. S.M.C.S.L. is funded by the European Research Council Consolidator (ERC-CoG-725722-OVOGROWTH). M.P. is supported by the Special Research Fund, Bijzonder Onderzoeksfonds (BOF01D08114). M.G. is supported by the Methusalem grant of Vrije Universiteit Brussel, in the name of Prof. Karen Sermon and by Innovation by Science and Technology in Flanders (IWT, Project Number: 150042). A.V. and B.A. are supported by the Plataforma de Proteomica, Genotipado y Lineas Celulares (PT1770019/0015) (PRB3), Instituto de Salud Carlos III. Research grant to B.H. by the Research Foundation-Flanders (FWO) (FWO.KAN.2016.0005.01 and FWO.Project G051516N). There are no conflicts of interest to declare.
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页数:20
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