Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-x5gtn Total loading time: 0 Render date: 2024-05-01T13:13:00.627Z Has data issue: false hasContentIssue false

Chapter 20.1 - Fetal stem cell transplantation

stem cell biology basics

from Section 2 - Fetal disease

Published online by Cambridge University Press:  05 February 2013

Mark D. Kilby
Affiliation:
Department of Fetal Medicine, University of Birmingham
Anthony Johnson
Affiliation:
Baylor College of Medicine, Texas
Dick Oepkes
Affiliation:
Department of Obstetrics, Leiden University Medical Center
Get access

Summary

Introduction

The term “stem cell” was originally used in the nineteenth century by embryologists to describe germ-line cells, that is, those that give rise to eggs and sperm. The first modern reference to stem cells came from scientists in the early 1960s when evidence was found of continuous cellular activity during neurogenesis in the brain. However, it was the hematologists Till and McCulloch who, in 1961, laid the foundations for future technological and conceptual advances in the field by demonstrating the presence of stem cells in the bone marrow [1]. Since then, and especially in the last 15 years, stem cell research has expanded exponentially.

Simply put, the driving force for the considerable interest in stem cells is the prospect that they represent a totally new approach to medicine in the twenty-first century. In particular, most excitement has been generated around the idea that stem cells can provide a limitless supply of tissue cell types for what is generally referred to as regenerative medicine, whether this be in the context of treatment of traumatic tissue damage or alleviation of the consequences of cellular loss brought about by disease or the result of ageing. However, there is more to the clinical application of stem cell biology knowledge than an off-the-shelf supply of large numbers of tissue cells. Hence, our ever-increasing understanding of stem cell biology is also likely to provide clues as to ways in which we might either influence the body’s own cellular replacement mechanisms for therapeutic benefit, for example, following severe ischemic damage in the brain or the heart, or overcome deficits in stem cell function that contribute partly or wholly to ageing in tissues such as muscle. Moreover, cancer has been shown to be underpinned by cells that have acquired aberrant stem cell-like properties, and it may prove possible to target these as a way of curtailing the development or progression of the disease.

Type
Chapter
Information
Fetal Therapy
Scientific Basis and Critical Appraisal of Clinical Benefits
, pp. 389 - 396
Publisher: Cambridge University Press
Print publication year: 2012

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Till, JE, McCulloch, EA. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat Res 1961;14:213–22.Google Scholar
Gurdon, JB, Elsdale, TR, Fischberg, M. Sexually mature individuals of Xenopus laevis from the transplantation of single somatic nuclei. Nature 1958;182:64–5.Google Scholar
Campbell, KH, McWhir, J, Ritchie, WA, Wilmut, I. Sheep cloned by nuclear transfer from a cultured cell line. Nature 1996;380:64–6.Google Scholar
Takahashi, K, Yamanaka, S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell 2006;126:663–76.Google Scholar
Takahashi, K, Tanabe, K, Ohnuki, M, et al. Induction of pluripotent stem cells from adult human fibroblasts by defined factors. Cell 2007;131:861–72.Google Scholar
Weissman, IL, Shizuru, JA. The origins of the identification and isolation of hematopoietic stem cells, and their capability to induce donor-specific transplantation tolerance and treat autoimmune diseases. Blood 2008;112:3543–53.Google Scholar
Goodell, MA, Brose, K, Paradis, G, Conner, AS, Mulligan, RC. Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo. J Exp Med 1996;183:1797–806.Google Scholar
Thomas, ED, Lochte, HL Jr, Lu, WC, Ferrebee, JW. Intravenous infusion of bone marrow in patients receiving radiation and chemotherapy. N Engl J Med 1957;257:491–6.Google Scholar
Macchiarini, P, Jungebluth, P, Go, T, et al. Clinical transplantation of a tissue-engineered airway. Lancet 2008;372:2023–30.Google Scholar
Unternaehrer, JJ, Daley, GQ. Induced pluripotent stem cells for modelling human diseases. Philos Trans R Soc Lond B Biol Sci 2011;366:2274–85.Google Scholar
Hanna, J, Wernig, M, Markoulaki, S, et al. Treatment of sickle cell anemia mouse model with iPS cells generated from autologous skin. Science 2007;318(5858):1920–3.Google Scholar
Urnov, FD, Rebar, EJ, Holmes, MC, Zhang, HS, Gregory, PD. Genome editing with engineered zinc finger nucleases. Nat Rev Genet 2010;11:636–46.Google Scholar
Murry, CE, Keller, G. Differentiation of embryonic stem cells to clinically relevant populations: lessons from embryonic development. Cell 2008;132:661–80.Google Scholar
Efe, JA, Ding, S.The evolving biology of small molecules: controlling cell fate and identity. Philos Trans R Soc Lond B Biol Sci 2011;366:2208–21.Google Scholar
Ott, HC, Matthiesen, TS, Goh, SK, et al. Perfusion-decellularized matrix: using nature’s platform to engineer a bioartificial heart. Nat Med 2008;14:213–21.Google Scholar
Baptista, PM, Siddiqui, MM, Lozier, G, et al. The use of whole organ decellularization for the generation of a vascularized liver organoid. Hepatology 2011;53:604–17.Google Scholar
Zanjani, ED, Pallavicini, MG, Ascensao, JL, et al. Engraftment and long-term expression of human fetal hemopoietic stem cells in sheep following transplantation in utero. J Clin Invest 1992;89:1178–88.Google Scholar
Boyd, AS, Fairchild, PJ. Approaches for immunological tolerance induction to stem cell-derived cell replacement therapies. Expert Rev Clin Immunol 2010;6:435–48.Google Scholar
Taylor, CJ, Bolton, EM, Bradley, JA. Immunological considerations for embryonic and induced pluripotent stem cell banking. Philos Trans R Soc Lond B Biol Sci 2011;366:2312–22.Google Scholar
Wilmut, I, Sullivan, G, Chambers, I. The evolving biology of cell reprogramming. Philos Trans R Soc Lond B Biol Sci 2011;366:2183–97.Google Scholar
Kim, K, Doi, A, Wen, B, et al. Epigenetic memory in induced pluripotent stem cells. Nature 2010;467:285–90.Google Scholar
Lister, R, Pelizzola, M, Kida, YS, et al. Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells. Nature 2011;471:68–73.Google Scholar
Gore, A, Li, Z, Fung, HL, et al. Somatic coding mutations in human induced pluripotent stem cells. Nature 2011;471:63–7.Google Scholar
Zhao, T, Zhang, ZN, Rong, Z, Xu, Y. Immunogenicity of induced pluripotent stem cells. Nature 2011;474:212–15.Google Scholar
Efe, JA, Hilcove, S, Kim, J, et al. Conversion of mouse fibroblasts into cardiomyocytes using a direct reprogramming strategy. Nat Cell Biol 2011;13:215–22.Google Scholar
Kim, J, Efe, JA, Zhu, S, et al. Direct reprogramming of mouse fibroblasts to neural progenitors. Proc Natl Acad Sci U S A 2011;108:7838–43.Google Scholar
Jopling, C, Sleep, E, Raya, M, et al. Zebrafish heart regeneration occurs by cardiomyocyte dedifferentiation and proliferation. Nature 2010;464:606–9.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×