Copyright
©The Author(s) 2015.
World J Gastroenterol. Jun 7, 2015; 21(21): 6591-6603
Published online Jun 7, 2015. doi: 10.3748/wjg.v21.i21.6591
Published online Jun 7, 2015. doi: 10.3748/wjg.v21.i21.6591
Figure 3 Increased necrotic area in the Dicer1-/- liver.
A: Hematoxylin-eosin stained liver tissue from Dicer1-/- mouse shows necrosis (Scale bar: 200 μm). The necrotic area is circled with black dotted lines; B: Quantitative analysis of necrotic area observed on HE stained sections (mean ± SD; n = 4-5), aP < 0.05 vs wild-type mice; C: ALT and AST serum levels in the wild-type and Dicer1-deficient mice at indicated time points (mean ± SD; n = 4-6), aP < 0.05 vs wild-type mice; D: IL-1α expression in Dicer1-/- liver was compared with control littermates (mean ± SD; n = 4), aP < 0.05 vs wild-type mice. ALT: Alanine amino-transferase; AST: Aspartate amino-transferase.
- Citation: Lu XF, Zhou YJ, Zhang L, Ji HJ, Li L, Shi YJ, Bu H. Loss of Dicer1 impairs hepatocyte survival and leads to chronic inflammation and progenitor cell activation. World J Gastroenterol 2015; 21(21): 6591-6603
- URL: https://www.wjgnet.com/1007-9327/full/v21/i21/6591.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i21.6591