Stable Expression of the Alkaline Phosphatase Marker Gene by Neural Cells in Culture and after Transplantation into the CNS Using Cells Derived from a Transgenic Rat

2002 ◽  
Vol 174 (1) ◽  
pp. 48-57 ◽  
Author(s):  
Tahmina Mujtaba ◽  
Steve S.W. Han ◽  
Itzhak Fischer ◽  
Eric P. Sandgren ◽  
Mahendra S. Rao
2004 ◽  
Vol 1 (1) ◽  
pp. 47-55 ◽  
Author(s):  
YUKINORI AKIYAMA ◽  
KAREN LANKFORD ◽  
CHRISTINE RADTKE ◽  
CHARLES A. GREER ◽  
JEFFERY D. KOCSIS

Transplantation of cell suspensions containing olfactory ensheathing cells (OECs) has been reported to remyelinate demyelinated axons in the spinal cord with a Schwann cell (SC)-like pattern of myelination. However, questions have been raised recently as to whether OECs can form SC-like myelin. To address this issue we prepared SCs and OECs from transgenic rats in which a marker gene, human placental alkaline phosphatase (hPAP), is linked to the ubiquitously active promoter of the R26 gene. SCs were prepared from the sciatic nerve and OECs from the outer nerve-fiber layer of the olfactory bulb. Positive S100 and p75 immunostaining indicated that >95% of cells in culture displayed either SC or OEC phenotypes. Suspensions of either SCs or OECs were transplanted into an X-irradiation/ethidium bromide demyelinating lesion in the spinal cord. We observed extensive SC-like remyelination following either SC or OEC transplantation 3 weeks after injection of the cells. Alkaline phosphatase (ALP) chromagen reaction product was associated clearly with the myelin-forming cells. Thus, cell suspensions that are enriched in either SCs or OECs result in peripheral-like myelin when transplanted in vivo.


2017 ◽  
Vol 12 (1) ◽  
pp. 294-299 ◽  
Author(s):  
Jianguo Han ◽  
Li Su ◽  
Chunyang Zhang ◽  
Rongcai Jiang

AbstractmicroRNAs (miRNAs) play an important role in osteoblast differentiation. However, the mechanisms of miRNAs regulating osteoblast mineralization still needs to be further cleared. Distal-less genes 2 (Dlx2) plays an important role in osteoblast differentiation. We have found that miR-539 was significantly downregulated and Dlx2 was found to be inversely correlated with miR-539 in MC3T3-E1 cell line during osteoblast mineralization. The overexpression of miR-539 significantly decreased the expression level of Dlx2 and suppressed the osteogenic marker gene expression level, alkaline phosphatase activity and matrix mineralization. Our study showed that miR-539 was a negative regulator in osteoblast mineralization and that the targeting of Dlx2 gene partly contributes to this inhibitory effect exerted by miR-539.


2020 ◽  
Vol 349 ◽  
pp. 577422
Author(s):  
Julie Pabois ◽  
Tony Durand ◽  
Catherine Le Berre ◽  
Jacques Gonzales ◽  
Michel Neunlist ◽  
...  

2001 ◽  
Vol 127 (2) ◽  
pp. 99-109 ◽  
Author(s):  
Richard C Krueger ◽  
Matthew T Santore ◽  
Glyn Dawson ◽  
Nancy B Schwartz

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