scholarly journals Notch pathway inhibitor DAPT accelerates in vitro proliferation and adipogenesis in infantile hemangioma stem cells

2021 ◽  
Vol 22 (6) ◽  
Author(s):  
Xing Xu ◽  
Yao Wu ◽  
Honghong Li ◽  
Juan Xie ◽  
Dongsheng Cao ◽  
...  
2011 ◽  
Vol 4 (1) ◽  
pp. 54 ◽  
Author(s):  
Dan Xu ◽  
Teresa M O ◽  
Archil Shartava ◽  
Taylor C Fowles ◽  
Jianchang Yang ◽  
...  

2015 ◽  
Vol 05 (999) ◽  
pp. 1-1
Author(s):  
Abu Bakar Mohd Hilmi ◽  
Mohd Noor Norhayati ◽  
Ahmad Sukari Halim ◽  
Chin Keong Lim ◽  
Zulkifli Mustafa ◽  
...  

2010 ◽  
Vol 125 (Supplement) ◽  
pp. 15
Author(s):  
CL Stewart ◽  
E Boscolo ◽  
JB Mulliken ◽  
J Bischoff

1995 ◽  
Vol 219 (1) ◽  
pp. 211-222 ◽  
Author(s):  
Donald P. Lennon ◽  
Stephen E. Haynesworth ◽  
Randell G. Young ◽  
James E. Dennis ◽  
Arnold I. Caplan

2011 ◽  
Vol 29 (9) ◽  
pp. 1327-1335 ◽  
Author(s):  
Argiris Papathanasopoulos ◽  
Dimitrios Kouroupis ◽  
Karen Henshaw ◽  
Dennis McGonagle ◽  
Elena A. Jones ◽  
...  

2007 ◽  
Vol 342-343 ◽  
pp. 165-168
Author(s):  
Sun Young Kook ◽  
You Young Jo ◽  
Hee Jung Lee ◽  
Byoung Moo Seo ◽  
Pill Hoon Choung

To ascertain the properties of human dental stem cells, various postnatal human stem cells were isolated from extracted human teeth and jawbones. Isolated dental stem cells were plated until losing their ‘stemness’ and were evaluated for their proliferation rate, colony forming efficiency, and expression of a specific stem cell marker. These dental stem cells have the potential to proliferate for more than 10 passages, except for the maxillary bone marrow stem cells (MXBMSCs). In particular, stem cells obtained from the periapical follicle (PAFSCs) were definitely superior to the other dental stem cells in proliferation, colony forming efficiency and expression of specific stem cells marker.


1992 ◽  
Vol 176 (2) ◽  
pp. 351-361 ◽  
Author(s):  
H Kodama ◽  
M Nose ◽  
Y Yamaguchi ◽  
J Tsunoda ◽  
T Suda ◽  
...  

The preadipose cell line, PA6, can support long-term hemopoiesis. Frequency of the hemopoietic stem cells capable of sustaining hemopoiesis in cocultures of bone marrow cells and PA6 cells for 6 wk was 1/5.3 x 10(4) bone marrow cells. In the group of dishes into which bone marrow cells had been inoculated at 2.5 x 10(4) cells/dish, 3 of 19 dishes (16%) contained stem cells capable of reconstituting erythropoiesis of WBB6F1-W/Wv mice, indicating that PA6 cells can support the proliferation of primitive hemopoietic stem cells. When the cocultures were treated with an antagonistic anti-c-kit monoclonal antibody, ACK2, only a small number of day 12 spleen colony-forming units survived; and hemopoiesis was severely reduced. However, when the cocultures were continued with antibody-free medium, hemopoiesis dramatically recovered. To examine the proliferative properties of the ACK2-resistant stem cells, we developed a colony assay system by modifying our coculture system. Sequential observations of the development of individual colonies and their disappearance demonstrated that the stem cells having higher proliferative capacity preferentially survive the ACK2 treatment. Furthermore, cells of subclones of the PA6 clone that were incapable of supporting long-term hemopoiesis expressed mRNA for the c-kit ligand. These results suggest that a mechanism(s) other than that involving c-kit receptor and its ligand plays an important role in the survival and proliferation of primitive hemopoietic stem cells.


2017 ◽  
Vol 67 (2) ◽  
pp. 183-196 ◽  
Author(s):  
Siegmund Lang ◽  
Marietta Herrmann ◽  
Christian Pfeifer ◽  
Gero Brockhoff ◽  
Johannes Zellner ◽  
...  

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