scholarly journals Transdifferentiation of stem cells: from the cell to the body

2021 ◽  
Vol 23 (3) ◽  
pp. 205-214
Author(s):  
Alexander V. Moskalev ◽  
Boris Yu. Gumilevsky ◽  
Vasiliy Ya. Apcel ◽  
Vasiliy N. Tsygan

The phases of embryo development, starting with the formation of gametes and germlines, are considered. This study described the differences in the selection of germ and somatic cells. The formation of true germ cells is associated with the induction of bone morphogenetic protein. The zinc-finger transcription factor is the marker of the formation of true germ cells in primates. True germ cells have two types: germ cells that form endoderm and those that form an epiblast. Their differentiation is provided by the growth factor of fibroblasts due to the signaling protein FGF4, which interacts with the FGFR2 receptor in the primary endoderm. The migration of germ cells is controlled by the factors of stromal cells. The implantation of a fertilized egg is associated with the peculiarities of the differentiation of the trophectoderm and the influence of transcription factors. Since stem cell lines are isolated from non-brain tissues, their origin and development remain not fully established. In mice, the chorion is formed from a small area of trophectoderm covered with an out-of-the-mouth mesoderm on the proximal end of the egg lumen. In humans, the chorion, together with its basisnon-embryonic mesodermis the earliest appearance of tissue emanating from the primary endoderm. Modern research has confirmed the possibility of obtaining clones from the nuclei of early blastomere embryos. However, the use of cell nuclei at later stages yielded unsatisfactory results. The use of embryonic stem nuclei has produced much better results than the use of cells in the later stages of development. Therefore, whatever the source of the cores, they should be in the G0 or G1 phase, but not in G2.

Blood ◽  
2006 ◽  
Vol 107 (2) ◽  
pp. 520-527 ◽  
Author(s):  
Jie Zheng ◽  
Kenji Kitajima ◽  
Eiko Sakai ◽  
Tohru Kimura ◽  
Naoko Minegishi ◽  
...  

AbstractThe zinc finger transcription factor GATA-1 is essential for both primitive (embryonic) and definitive (adult) erythropoiesis. To define the roles of GATA-1 in the production and differentiation of primitive and definitive erythrocytes, we established GATA-1-null embryonic stem cell lines in which GATA-1 was able to be conditionally expressed by using the tetracycline conditional gene expression system. The cells were subjected to hematopoietic differentiation by coculturing on OP9 stroma cells. We expressed GATA-1 in the course of primitive and definitive erythropoiesis and analyzed the ability of GATA-1 to rescue the defective erythropoiesis caused by the GATA-1 null mutation. Our results show that GATA-1 functions in the proliferation and maturation of erythrocytes in a distinctive manner. The early-stage expression of GATA-1 during both primitive and definitive erythropoiesis was sufficient to promote the proliferation of red blood cells. In contrast, the late-stage expression of GATA-1 was indispensable to the terminal differentiation of primitive and definitive erythrocytes. Thus, GATA-1 affects the proliferation and differentiation of erythrocytes by different mechanisms.


2010 ◽  
Vol 32 (5) ◽  
pp. 11-13
Author(s):  
Sarah Cooper

Advocates of embryonic stem (ES) cells have promised much from this technology, from reversal of neurodegenerative diseases to custom tissue regeneration. What is it, then, that makes ES cells so remarkable? Essentially, this question can be answered by two major features: an ability to self-renew and thereby divide indefinitely in culture, and pluripotency, the ability to respond to external signals and differentiate into any type of cell in the body, including germ cells.


2010 ◽  
Vol 38 (4) ◽  
pp. 1051-1057 ◽  
Author(s):  
Delphine Laustriat ◽  
Jacqueline Gide ◽  
Marc Peschanski

Human pluripotent stem cells are a biological resource most commonly considered for their potential in cell therapy or, as it is now called, ‘regenerative medicine’. However, in the near future, their most important application for human health may well be totally different, as they are more and more envisioned as opening new routes for pharmacological research. Pluripotent stem cells indeed possess the main attributes that make them theoretically fully equipped for the development of cell-based assays in the fields of drug discovery and predictive toxicology. These cells are characterized by: (i) an unlimited self-renewal capacity, which make them an inexhaustible source of cells; (ii) the potential to differentiate into any cell phenotype of the body at any stage of differentiation, with probably the notable exception, however, of the most mature forms of many lineages; and (iii) the ability to express genotypes of interest via the selection of donors, whether they be of embryonic origin, through pre-implantation genetic diagnosis, or adults, by genetic reprogramming of somatic cells, so-called iPSCs (induced pluripotent stem cells). In the present review, we provide diverse illustrations of the use of pluripotent stem cells in drug discovery and predictive toxicology, using either human embryonic stem cell lines or iPSC lines.


2005 ◽  
Vol 22 (3) ◽  
pp. 152-158
Author(s):  
Sayaka Wakayama ◽  
Masashi Miyake ◽  
Teruhiko Wakayama

Cells ◽  
2019 ◽  
Vol 8 (3) ◽  
pp. 226 ◽  
Author(s):  
Hirokazu Tanaka ◽  
J. Espinoza ◽  
Ryosuke Fujiwara ◽  
Shinya Rai ◽  
Yasuyoshi Morita ◽  
...  

Iron overload is the accumulation of excess iron in the body that may occur as a result of various genetic disorders or as a consequence of repeated blood transfusions. The surplus iron is then stored in the liver, pancreas, heart and other organs, which may lead to chronic liver disease or cirrhosis, diabetes and heart disease, respectively. In addition, excessive iron may impair hematopoiesis, although the mechanisms of this deleterious effect is not entirely known. In this study, we found that ferrous ammonium sulfate (FeAS), induced growth arrest and apoptosis in immature hematopoietic cells, which was mediated via reactive oxygen species (ROS) activation of p38MAPK and JNK pathways. In in vitro hematopoiesis derived from embryonic stem cells (ES cells), FeAS enhanced the development of dysplastic erythroblasts but inhibited their terminal differentiation; in contrast, it had little effect on the development of granulocytes, megakaryocytes, and B lymphocytes. In addition to its directs effects on hematopoietic cells, iron overload altered the expression of several adhesion molecules on stromal cells and impaired the cytokine production profile of these cells. Therefore, excessive iron would affect whole hematopoiesis by inflicting vicious effects on both immature hematopoietic cells and stromal cells.


2009 ◽  
Vol 18 (5) ◽  
pp. 704-716 ◽  
Author(s):  
S Deleu ◽  
E Gonzalez-Merino ◽  
N Gaspard ◽  
TMU Nguyen ◽  
P Vanderhaeghen ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (10) ◽  
pp. e0164664 ◽  
Author(s):  
Yani Zhang ◽  
Yingjie Wang ◽  
Qisheng Zuo ◽  
Xiaoyan Wang ◽  
Dong Li ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document