scholarly journals Abetalipoproteinaemia arising from a new variant of microsomal triglyceride transfer protein in a child presenting with chronic fat malabsorption

2021 ◽  
Vol 15 (1) ◽  
pp. 53
Author(s):  
CB Eke ◽  
AD Marais ◽  
RJ De Lacy ◽  
AJ Hooper ◽  
BD Ratanjee ◽  
...  
2000 ◽  
Vol 41 (8) ◽  
pp. 1199-1204 ◽  
Author(s):  
Ken Ohashi ◽  
Shun Ishibashi ◽  
Jun-ichi Osuga ◽  
Ryu-ichi Tozawa ◽  
Kenji Harada ◽  
...  

2006 ◽  
Vol 130 (6) ◽  
pp. 1661-1669 ◽  
Author(s):  
Silvia Mirandola ◽  
Stefano Realdon ◽  
Jahangir Iqbal ◽  
Martina Gerotto ◽  
Francesca Dal Pero ◽  
...  

2008 ◽  
Vol 49 (9) ◽  
pp. 2013-2022 ◽  
Author(s):  
Zhouji Chen ◽  
Elizabeth P. Newberry ◽  
Jin Y. Norris ◽  
Yan Xie ◽  
Jianyang Luo ◽  
...  

2013 ◽  
Vol 288 (20) ◽  
pp. 14372-14383 ◽  
Author(s):  
Joby Josekutty ◽  
Jahangir Iqbal ◽  
Takao Iwawaki ◽  
Kenji Kohno ◽  
M. Mahmood Hussain

Microsomal triglyceride transfer protein (MTP) is a target to reduce plasma lipids because of its indispensable role in triglyceride-rich lipoprotein biosynthesis. MTP inhibition in Western diet fed mice decreased plasma triglycerides/cholesterol, whereas increasing plasma alanine/aspartate aminotransferases (ALT/AST) and hepatic triglycerides/free cholesterol. Free cholesterol accumulated in the endoplasmic reticulum (ER) and mitochondria resulting in ER and oxidative stresses. Mechanistic studies revealed that MTP inhibition increased transcription of the GPT/GOT1 genes through up-regulation of the IRE1α/cJun pathway leading to increased synthesis and release of ALT1/AST1. Thus, transcriptional up-regulation of GPT/GOT1 genes is a major mechanism, in response to ER stress, elevating plasma transaminases. Increases in plasma and tissue transaminases might represent a normal response to stress for survival.


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