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World Stem Cell Summit 2010

Saturday, February 6, 2010

ScienceDirect Alert: Cell Stem Cell, Vol. 6, Iss. 2, 2010


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Cell Stem CellCell Stem Cell

Volume 6, Issue 2,  Pages 91-182 (5 February 2010)


 1. Editors' Notes
Page xi


 
  Previews
 2. A New Member of the Spindle Orientation Club: Mammalian Intestinal Stem Cells
Pages 91-92
Yukiko M. Yamashita

 
 3. Age-Related Changes in Niche Cells Influence Hematopoietic Stem Cell Function
Pages 93-94
Erin J. Oakley, Gary Van Zant

 
 4. A Dominant Role of the Hair Follicle Stem Cell Niche in Regulating Melanocyte Stemness
Pages 95-96
Cédric Blanpain, Panagiota A. Sotiropoulou

 
 5. NO Signals from the Cancer Stem Cell Niche
Pages 97-98
Joan Seoane

 
  Forum
 6. A Legal Defense for Compensating Research Egg Donors
Pages 99-102
Susan L. Crockin

 
  Review
 7. Stem Cells and the Niche: A Dynamic Duo
Pages 103-115
Justin Voog, D. Leanne Jones

 
  Articles
 8. Sprouty1 Regulates Reversible Quiescence of a Self-Renewing Adult Muscle Stem Cell Pool during Regeneration
Pages 117-129
Kelly L. Shea, Wanyi Xiang, Vincent S. LaPorta, Jonathan D. Licht, Charles Keller, M. Albert Basson, Andrew S. Brack

Graphical Abstract

Pax7+ skeletal satellite cells regenerate muscle in their endogenous environment ► Quiescent satellite cells express the RTK inhibitor Spry1Spry1 is needed for satellite cells to return to quiescence after muscle injury ► Deletion of Spry1 in satellite cells depletes the muscle stem cell pool


 
 9. Key Roles for Transforming Growth Factor β in Melanocyte Stem Cell Maintenance
Pages 130-140
Emi K. Nishimura, Misa Suzuki, Vivien Igras, Jinyan Du, Scott Lonning, Yoshiki Miyachi, Jürgen Roes, Friedrich Beermann, David E. Fisher

Graphical Abstract

► TGF-β signaling active as melanocyte stem cells enter quiescence ► TGF-β from niche induces cell cycle arrest and suppresses melanogenic genes ► Deletion of TGF-β receptor depletes melanocyte stem cells ► Hair grays prematurely in mice lacking melanocyte TFG-β receptor


 
 10. Perivascular Nitric Oxide Activates Notch Signaling and Promotes Stem-like Character in PDGF-Induced Glioma Cells
Pages 141-152
Nikki Charles, Tatsuya Ozawa, Massimo Squatrito, Anne-Marie Bleau, Cameron W. Brennan, Dolores Hambardzumyan, Eric C. Holland

Graphical Abstract

► Perivascular niche nitric oxide activates Notch in PDGF-induced gliomas ► Notch signaling drives tumor stem-like characteristics and reduces survival ► Loss of eNOS activity decreases tumor stem-like characteristics ► Suppressing eNOS activity prolongs survival in glioma-bearing mice


 
 11. Polycomb-like 2 Associates with PRC2 and Regulates Transcriptional Networks during Mouse Embryonic Stem Cell Self-Renewal and Differentiation
Pages 153-166
Emily Walker, Wing Y. Chang, Julie Hunkapiller, Gerard Cagney, Kamal Garcha, Joseph Torchia, Nevan J. Krogan, Jeremy F. Reiter, William L. Stanford

Graphical Abstract

► PCL2 associates with the PRC2 complex in mouse ESCs ► PCL2 knockdown increases self-renewal and disrupts differentiation ► Reducing PLC2 decreases H3K27me3 at specific targets ► PCL2 represses transcription of self-renewal genes in ESCs


 
  Short Articles
 12. The Nuclear Receptor Nr5a2 Can Replace Oct4 in the Reprogramming of Murine Somatic Cells to Pluripotent Cells
Pages 167-174
Jian-Chien Dominic Heng, Bo Feng, Jianyong Han, Jianming Jiang, Petra Kraus, Jia-Hui Ng, Yuriy L. Orlov, Mikael Huss, Lin Yang, Thomas Lufkin, Bing Lim, Huck-Hui Ng

Graphical Abstract

► Nuclear receptor Nr5a2 enhances reprogramming of mouse fibroblasts ► Nr5a2 can replace Oct4 in the reprogramming cocktail ► Nr5a2 with enhanced transcriptional activity more effective in reprogramming ► DNA binding links Nr5a2 to the core pluripotency network


 
 13. Spindle Orientation Bias in Gut Epithelial Stem Cell Compartments Is Lost in Precancerous Tissue
Pages 175-181
Aaron J. Quyn, Paul L. Appleton, Francis A. Carey, Robert J.C. Steele, Nick Barker, Hans Clevers, Rachel A. Ridgway, Owen J. Sansom, Inke S. Näthke

Graphical Abstract

► Mitotic spindles in intestinal stem cells align perpendicularly ► In precancerous tissue, this spindle orientation bias is lost ► Spindle alignment correlates with segregation of unreplicated DNA ► Loss of unreplicated DNA occurs more quickly in precancerous tissue


 


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