scholarly journals Quantitation of apolipoprotein E mRNA in the liver and peripheral tissues of nonhuman primates.

1985 ◽  
Vol 260 (4) ◽  
pp. 2452-2457 ◽  
Author(s):  
T C Newman ◽  
P A Dawson ◽  
L L Rudel ◽  
D L Williams
1985 ◽  
Vol 260 (4) ◽  
pp. 2444-2451 ◽  
Author(s):  
D L Williams ◽  
P A Dawson ◽  
T C Newman ◽  
L L Rudel

1985 ◽  
Vol 454 (1) ◽  
pp. 222-229 ◽  
Author(s):  
DAVID L. WILLIAMS ◽  
PAUL A. DAWSON ◽  
THOMAS C. NEWMAN ◽  
LAWRENCE L. RUDEL

2020 ◽  
Author(s):  
Hyunah Lee ◽  
Graham D. Cocks ◽  
Paulina Nowosiad ◽  
Lucia M. Dutan Polit ◽  
Jack Price ◽  
...  

Abstract Apolipoprotein E (ApoE) is a multifunctional protein that plays significant roles in important cellular mechanisms in peripheral tissues and is as well expressed in the central nervous system, notably by adult neural stem cells (NSCs) in the hippocampus. Evidence from animal studies suggest that ApoE is critical for adult NSC maintenance. However, whether ApoE has the potential to play a similar role in human NSCs has not been directly investigated. To address this question, we conducted a focused study on APOE gene expression level using an in vitro model of neural differentiation and human induced pluripotent stem cells derived from a neurotypical individual. We found that APOE expression was dramatically decreased as the cells became more differentiated, indicating that APOE expression levels reflect the degree of cellular differentiation during neural induction suggesting a potential role for ApoE in human NSC maintenance. Our findings justify further investigations being carried out to understand whether changes in APOE level can directly impact the neurogenic capacity of human stem cells.


F1000Research ◽  
2020 ◽  
Vol 9 ◽  
pp. 353
Author(s):  
Hyunah Lee ◽  
Paulina Nowosiad ◽  
Lucia M. Dutan Polit ◽  
Jack Price ◽  
Deepak P. Srivastava ◽  
...  

Apolipoprotein E (APOE) is a multifunctional protein that plays significant roles in important cellular mechanisms in peripheral tissues and is as well expressed in the central nervous system, notably by adult neural stem cells (NSCs) in the hippocampus. Evidence from animal studies suggest that APOE is critical for adult NSC maintenance. However, whether APOE has the potential to play a similar role in human NSCs has not been directly investigated. To address this question, we conducted a focused study characterising APOE gene and protein expression in an in vitro model of neural differentiation utilising human induced pluripotent stem cells. We found that APOE gene expression was dramatically decreased as the cells became more differentiated, indicating that APOE expression levels reflect the degree of cellular differentiation during neural induction. Furthermore, qualitative analysis results of immunocytochemistry showed that intracellular localisation of APOE protein becomes more pronounced as neural differentiation progresses. Taken together, our findings suggest a potential role for APOE in human NSC maintenance and justify further investigations being carried out to understand whether changes in APOE levels can directly impact the neurogenic capacity of human stem cells.


F1000Research ◽  
2020 ◽  
Vol 9 ◽  
pp. 353
Author(s):  
Hyunah Lee ◽  
Paulina Nowosiad ◽  
Lucia M. Dutan Polit ◽  
Jack Price ◽  
Deepak P. Srivastava ◽  
...  

Apolipoprotein E (APOE) is a multifunctional protein that plays significant roles in important cellular mechanisms in peripheral tissues and is as well expressed in the central nervous system, notably by adult neural stem cells (NSCs) in the hippocampus. Evidence from animal studies suggest that APOE is critical for adult NSC maintenance. However, whether APOE has the potential to play a similar role in human NSCs has not been directly investigated. To address this question, we conducted a focused study characterising APOE gene and protein expression in an in vitro model of neural differentiation utilising human induced pluripotent stem cells. We found that APOE gene expression was dramatically decreased as the cells became more differentiated, indicating that APOE expression levels reflect the degree of cellular differentiation during neural induction. Furthermore, qualitative analysis results of immunocytochemistry showed that intracellular localisation of APOE protein becomes more pronounced as neural differentiation progresses. Taken together, our findings suggest a potential role for APOE in human NSC maintenance and justify further investigations being carried out to understand whether changes in APOE levels can directly impact the neurogenic capacity of human stem cells.


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