Grigori Enikolopov

Dr. Grigori Enikolopov


Research Focus & Metrics

Academic Career Length

50Years (1977-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 August 2010 in Nature
Verified
Journal Article
Closed access
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SMSimón Méndez-Ferrer
Simón Méndez-Ferrer
TMTatyana V. Michurina
Tatyana V. Michurina
FFFrancesca Ferraro
Francesca Ferraro
AMAmin R. Mazloom
Amin R. Mazloom
BMBen D. MacArthur
Ben D. MacArthur
PFPaul S. Frenette
Paul S. Frenette

25 January 2012 in Nature
Verified
Journal Article
Open access
PDF file
LDLei Ding
Lei Ding
TSThom Saunders
Thom Saunders
GEGrigori Enikolopov
Grigori Enikolopov
SMSean J. Morrison
Sean J. Morrison
Several cell types have been proposed to create niches for haematopoietic stem cells (HSCs). However, the expression patterns of HSC maintenance factors have not been systematically studied and no such factor has been conditionally deleted from any candidate niche cell. Thus, the cellular sources of these factors are undetermined. Stem cell factor (SCF; also known as KITL) is a key niche component that maintains HSCs. Here, using Scfgfp knock-in mice, we found that Scf was primarily expressed by perivascular cells throughout the bone marrow. HSC frequency and function were not affected when Scf was conditionally deleted from haematopoietic cells, osteoblasts, nestin-cre- or nestin-creER-expressing cells. However, HSCs were depleted from bone marrow when Scf was deleted from endothelial cells or leptin receptor (Lepr)-expressing perivascular stromal cells. Most HSCs were lost when Scf was deleted from both endothelial and Lepr-expressing perivascular cells. Thus, HSCs reside in a perivascular niche in which multiple cell types express factors that promote HSC maintenance.

1 October 2010 in Cell Stem Cell
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Journal Article
Closed access
ASAmanda Sierra
Amanda Sierra
JEJuan M. Encinas
Juan M. Encinas
JDJuan J.P. Deudero
Juan J.P. Deudero
JCJessica H. Chancey
Jessica H. Chancey
GEGrigori Enikolopov
Grigori Enikolopov
MMMirjana Maletic-Savatic
Mirjana Maletic-Savatic

1 May 2011 in Cell Stem Cell
Verified
Journal Article
Closed access
JEJuan M. Encinas
Juan M. Encinas
TMTatyana V. Michurina
Tatyana V. Michurina
NPNatalia Peunova
Natalia Peunova
JPJune-Hee Park
June-Hee Park
JTJulie Tordo
Julie Tordo
GEGrigori Enikolopov
Grigori Enikolopov

12 January 2004 in Journal of Comparative Neurology
Verified
Journal Article
Closed access
PDF file
JMJohn L. Mignone
John L. Mignone
VKValery Kukekov
Valery Kukekov
ACAnn‐Shyn Chiang
Ann‐Shyn Chiang
DSDennis Steindler
Dennis Steindler
GEGrigori Enikolopov
Grigori Enikolopov

23 May 2006 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Closed access
JEJuan M. Encinas
Juan M. Encinas
AVAnne Vaahtokari
Anne Vaahtokari
GEGrigori Enikolopov
Grigori Enikolopov
Chronic treatment with antidepressants increases neurogenesis in the adult hippocampus. This increase in the production of new neurons may be required for the behavioral effects of antidepressants. However, it is not known which class of cells within the neuronal differentiation cascade is targeted by the drugs. We have generated a reporter mouse line, which allows identification and classification of early neuronal progenitors. It also allows accurate quantitation of changes induced by neurogenic agents in these distinct subclasses of neuronal precursors. We use this line to demonstrate that the selective serotonin reuptake inhibitor antidepressant fluoxetine does not affect division of stem-like cells in the dentate gyrus but increases symmetric divisions of an early progenitor cell class. We further demonstrate that these cells are the sole class of neuronal progenitors targeted by fluoxetine in the adult brain and suggest that the fluoxetine-induced increase in new neurons arises as a result of the expansion of this cell class. This finding defines a cellular target for antidepressant drug therapies.