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在禁食状态下,C57BL/6 小鼠肝脏中 PPARα 靶基因的表达需要 TIS21 基因。

PPARα-Target Gene Expression Requires TIS21 Gene in Liver of the C57BL/6 Mice under Fasting Condition.

机构信息

Ajou Graduate School of medicine, Suwon 16499, Republic of Korea.

BK Plus program, Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon 16499, Korea.

出版信息

Mol Cells. 2018 Feb 28;41(2):140-149. doi: 10.14348/molcells.2018.2257. Epub 2018 Jan 29.

Abstract

The TIS21 gene belongs to the antiproliferative gene (APRO) family and exhibits tumor suppressive activity. However, here we report that TIS21 controls lipid metabolism, rather than cell proliferation, under fasting condition. Using microarray analysis, whole gene expression changes were investigated in liver of TIS21 knockout (TIS21-KO) mice after 20 h fasting and compared with wild type (WT). Peroxisome proliferator-activated receptor alpha (PPARα) target gene expression was almost absent in contrast to increased lipid synthesis in the TIS21-KO mice compared to WT mice. Immunohistochemistry with hematoxylin and eosin staining revealed that lipid deposition was focal in the TIS21-KO liver as opposed to the diffuse and homogeneous pattern in the WT liver after 24 h starvation. In addition, cathepsin E expression was over 10 times higher in the TIS21-KO liver than that in the WT, as opposed to the significant reduction of thioltransferase in both adult and fetal livers. At present, we cannot account for the role of cathepsin E. However, downregulation of glutaredoxin 2 thioltransferase expression might affect hypoxic damage in the TIS21-KO liver. We suggest that the TIS21 gene might be essential to maintain energy metabolism and reducing power in the liver under fasting condition.

摘要

TIS21 基因属于增殖抑制基因(APRO)家族,具有肿瘤抑制活性。然而,在这里我们报告 TIS21 在禁食条件下控制脂质代谢,而不是细胞增殖。通过微阵列分析,研究了 TIS21 敲除(TIS21-KO)小鼠在禁食 20 小时后的肝脏中全基因表达的变化,并与野生型(WT)进行了比较。与 WT 相比,TIS21-KO 小鼠的过氧化物酶体增殖物激活受体 α(PPARα)靶基因表达几乎不存在,而脂质合成增加。苏木精和伊红染色的免疫组织化学显示,与 WT 肝脏中弥散且均匀的模式相比,TIS21-KO 肝脏中的脂质沉积呈局灶性。此外,TIS21-KO 肝脏中的组织蛋白酶 E 表达水平比 WT 肝脏高 10 倍以上,而两种成体和胎肝中的硫转移酶则显著降低。目前,我们还不能解释组织蛋白酶 E 的作用。然而,谷胱甘肽还原酶 2 硫转移酶表达的下调可能会影响 TIS21-KO 肝脏中的缺氧损伤。我们认为,TIS21 基因可能是维持肝脏在禁食条件下能量代谢和还原力所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a6a/5824024/8d739b4a8e49/molce-41-2-140f1.jpg

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