-
Je něco špatně v tomto záznamu ?
The origin, in vitro differentiation, and stemness specificity of progenitor cells
W. Kranc, J. Budna, M. Dudek, A. Bryja, A. Chachuła, S. Ciesiółka, S. Borys, M. Dyszkiewicz-Konwińska, M. Jeseta, L. Porowski, P. Antosik, D. Bukowska, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
Jazyk angličtina Země Itálie
Typ dokumentu časopisecké články
PubMed
28685538
Knihovny.cz E-zdroje
- MeSH
- buněčná a tkáňová terapie metody trendy MeSH
- buněčná diferenciace fyziologie MeSH
- folikulární buňky cytologie fyziologie MeSH
- kmenové buňky cytologie fyziologie MeSH
- leukemický inhibiční faktor metabolismus MeSH
- lidé MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Since the successful collection of the first progenitor stem cells (SCs), there has been an increased interest in these cells as a model for undiscovered and unlimited potential of differentiation and development. Additionally, it was shown that SC populations display an ability to form pluripotent and/or totipotent cell populations. It was found that human ovarian granulosa cells (GCs) maintain a large capacity for differentiation into several other cell lineages, such as chondrogenic, osteogenic, neurogenic, and adipogenic, particularly during long-term, in vitro culture. In these cases, the specific media supplements that promote various pathways of differentiation, such as leukemia-inhibiting factor (LIF) and/or FSH, are well recognized. However, these are only some examples of the differentiation possibilities of human SCs in vitro and other pathways still require further investigation. Many SC populations, which are directed to differentiate into specific cell types, are also successfully used in several human disease therapies, e.g. leukemia. Moreover, SCs are used for tissue scaffold construction in patients with respiratory and cardiovascular diseases. In this review, the most recent knowledge about the in vitro growth and differentiation capacity of SCs is presented. Furthermore, we discuss the possible worldwide application of SCs in advanced cell and tissue bioengineering. In conclusion, it is suggested that, in the future, SCs will be a basic strategy in human therapy, and their use will open new gates in regenerative and reconstructive medicine in the 21st century.
Department of Anatomy Poznan University of Medical Sciences Poznan Poland
Department of Histology and Embryology Poznan University of Medical Sciences Poznan Poland
Institute of Veterinary Sciences Poznan University of Life Sciences Poznan Poland
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17030701
- 003
- CZ-PrNML
- 005
- 20171102123022.0
- 007
- ta
- 008
- 171025s2017 it f 000 0|eng||
- 009
- AR
- 035 __
- $a (PubMed)28685538
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a it
- 100 1_
- $a Kranc, W $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 245 14
- $a The origin, in vitro differentiation, and stemness specificity of progenitor cells / $c W. Kranc, J. Budna, M. Dudek, A. Bryja, A. Chachuła, S. Ciesiółka, S. Borys, M. Dyszkiewicz-Konwińska, M. Jeseta, L. Porowski, P. Antosik, D. Bukowska, KP. Brüssow, M. Bruska, M. Nowicki, M. Zabel, B. Kempisty,
- 520 9_
- $a Since the successful collection of the first progenitor stem cells (SCs), there has been an increased interest in these cells as a model for undiscovered and unlimited potential of differentiation and development. Additionally, it was shown that SC populations display an ability to form pluripotent and/or totipotent cell populations. It was found that human ovarian granulosa cells (GCs) maintain a large capacity for differentiation into several other cell lineages, such as chondrogenic, osteogenic, neurogenic, and adipogenic, particularly during long-term, in vitro culture. In these cases, the specific media supplements that promote various pathways of differentiation, such as leukemia-inhibiting factor (LIF) and/or FSH, are well recognized. However, these are only some examples of the differentiation possibilities of human SCs in vitro and other pathways still require further investigation. Many SC populations, which are directed to differentiate into specific cell types, are also successfully used in several human disease therapies, e.g. leukemia. Moreover, SCs are used for tissue scaffold construction in patients with respiratory and cardiovascular diseases. In this review, the most recent knowledge about the in vitro growth and differentiation capacity of SCs is presented. Furthermore, we discuss the possible worldwide application of SCs in advanced cell and tissue bioengineering. In conclusion, it is suggested that, in the future, SCs will be a basic strategy in human therapy, and their use will open new gates in regenerative and reconstructive medicine in the 21st century.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a buněčná diferenciace $x fyziologie $7 D002454
- 650 _2
- $a buněčná a tkáňová terapie $x metody $x trendy $7 D064987
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a folikulární buňky $x cytologie $x fyziologie $7 D006107
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a leukemický inhibiční faktor $x metabolismus $7 D053605
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a kmenové buňky $x cytologie $x fyziologie $7 D013234
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Budna, J $u Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Dudek, M $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Bryja, A $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Chachuła, A $u Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Ciesiółka, S $u Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Borys, S $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Dyszkiewicz-Konwińska, M $u Department of Biomaterials and Experimental Dentistry, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Jeseta, M $u Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czech Republic.
- 700 1_
- $a Porowski, L $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Antosik, P $u Institute of Veterinary Sciences, Poznan University of Life Sciences, Poznan, Poland. $7 gn_A_00007535
- 700 1_
- $a Bukowska, D $u Institute of Veterinary Sciences, Poznan University of Life Sciences, Poznan, Poland.
- 700 1_
- $a Brüssow, K P $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Bruska, M $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Nowicki, M $u Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
- 700 1_
- $a Zabel, M $u Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland. Department of Histology and Embryology, Wroclaw Medical University, Wroclaw, Poland.
- 700 1_
- $a Kempisty, B $u Department of Anatomy, Poznan University of Medical Sciences, Poznan, Poland. Department of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland.
- 773 0_
- $w MED00008336 $t Journal of biological regulators and homeostatic agents $x 0393-974X $g Roč. 31, č. 2 (2017), s. 365-369
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28685538 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20171025 $b ABA008
- 991 __
- $a 20171102123115 $b ABA008
- 999 __
- $a ok $b bmc $g 1254294 $s 991728
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 31 $c 2 $d 365-369 $i 0393-974X $m Journal of Biological Regulators & Homeostatic Agents $n J Biol Regul Homeost Agents $x MED00008336
- LZP __
- $a Pubmed-20171025