Literature DB >> 22308291

Hematopoietic stem cells: to be or Notch to be.

Anna Bigas1, Lluis Espinosa.   

Abstract

Notch is a well-conserved signaling pathway and its function in cell fate determination is crucial in embryonic development and in the maintenance of tissue homeostasis during adult life. Notch activation depends on cell-cell interactions that are essential for the generation of cell diversity from initially equivalent cell populations. In the adult hematopoiesis, Notch is undoubtedly a very efficient promoter of T-cell differentiation, and this has masked for a long time the effects of Notch on other blood lineages, which are gradually being identified. However, the adult hematopoietic stem cell (HSC) remains mostly refractory to Notch intervention in experimental systems. In contrast, Notch is essential for the generation of the HSCs, which takes place during embryonic development. This review summarizes the knowledge accumulated in recent years regarding the role of the Notch pathway in the different stages of HSC ontology from embryonic life to fetal and adult bone marrow stem cells. In addition, we briefly examine other systems where Notch regulates specific stem cell capacities, in an attempt to understand how Notch functions in stem cell biology.

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Substances:

Year:  2012        PMID: 22308291     DOI: 10.1182/blood-2011-10-355826

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  54 in total

1.  NOTCH Activation at the Hematovascular Mesoderm Stage Facilitates Efficient Generation of T Cells with High Proliferation Potential from Human Pluripotent Stem Cells.

Authors:  Akhilesh Kumar; Jeong Hee Lee; Kran Suknuntha; Saritha S D'Souza; Abir S Thakur; Igor I Slukvin
Journal:  J Immunol       Date:  2018-12-21       Impact factor: 5.422

Review 2.  Wharton's Jelly Mesenchymal Stromal Cells as a Feeder Layer for the Ex Vivo Expansion of Hematopoietic Stem and Progenitor Cells: a Review.

Authors:  Melania Lo Iacono; Rita Anzalone; Giampiero La Rocca; Elena Baiamonte; Aurelio Maggio; Santina Acuto
Journal:  Stem Cell Rev Rep       Date:  2017-02       Impact factor: 5.739

Review 3.  Pleiotropic roles of Notch signaling in normal, malignant, and developmental hematopoiesis in the human.

Authors:  Rahul Kushwah; Borhane Guezguez; Jung Bok Lee; Claudia I Hopkins; Mickie Bhatia
Journal:  EMBO Rep       Date:  2014-09-24       Impact factor: 8.807

4.  Developmental exposure to 2,3,7,8 tetrachlorodibenzo-p-dioxin attenuates later-life Notch1-mediated T cell development and leukemogenesis.

Authors:  Lori S Ahrenhoerster; Tess C Leuthner; Everett R Tate; Peter A Lakatos; Michael D Laiosa
Journal:  Toxicol Appl Pharmacol       Date:  2015-01-10       Impact factor: 4.219

5.  HoxBlinc RNA Recruits Set1/MLL Complexes to Activate Hox Gene Expression Patterns and Mesoderm Lineage Development.

Authors:  Changwang Deng; Ying Li; Lei Zhou; Joonseok Cho; Bhavita Patel; Naohiro Terada; Yangqiu Li; Jörg Bungert; Yi Qiu; Suming Huang
Journal:  Cell Rep       Date:  2015-12-24       Impact factor: 9.423

6.  Splenic hematopoietic stem cells display a pre-activated phenotype.

Authors:  Emilie Coppin; Jonathan Florentin; Sathish Babu Vasamsetti; Anagha Arunkumar; John Sembrat; Mauricio Rojas; Partha Dutta
Journal:  Immunol Cell Biol       Date:  2018-03-11       Impact factor: 5.126

7.  Hes1 suppresses acute myeloid leukemia development through FLT3 repression.

Authors:  T Kato; M Sakata-Yanagimoto; H Nishikii; M Ueno; Y Miyake; Y Yokoyama; Y Asabe; Y Kamada; H Muto; N Obara; K Suzukawa; Y Hasegawa; I Kitabayashi; K Uchida; A Hirao; H Yagita; R Kageyama; S Chiba
Journal:  Leukemia       Date:  2014-09-19       Impact factor: 11.528

Review 8.  Regulation of endothelial cell differentiation and specification.

Authors:  Kathrina L Marcelo; Lauren C Goldie; Karen K Hirschi
Journal:  Circ Res       Date:  2013-04-26       Impact factor: 17.367

Review 9.  The biochemistry of hematopoietic stem cell development.

Authors:  P Kaimakis; M Crisan; E Dzierzak
Journal:  Biochim Biophys Acta       Date:  2012-10-12

10.  Microfibril-associated glycoprotein 2 (MAGP2) loss of function has pleiotropic effects in vivo.

Authors:  Michelle D Combs; Russell H Knutsen; Thomas J Broekelmann; Holly M Toennies; Thomas J Brett; Chantel A Miller; Daniel L Kober; Clarissa S Craft; Jeffrey J Atkinson; J Michael Shipley; Barbara C Trask; Robert P Mecham
Journal:  J Biol Chem       Date:  2013-08-20       Impact factor: 5.157

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