Expression of Hepatoma-derived growth factor family members in the adult central nervous system

作者: HebaM El-Tahir , Frank Dietz , Ralf Dringen , Kerstin Schwabe , Karen Strenge

DOI: 10.1186/1471-2202-7-6

关键词:

摘要: Hepatoma-derived growth factor (HDGF) belongs to a polypeptide family containing five additional members called HDGF related proteins 1–4 (HRP-1 -4) and Lens epithelial derived factor. Whereas some such as HRP-2 are expressed in wide range of tissues, the expression others is very restricted. HRP-1 -4 only testis, HRP-3 nervous system. Here we investigated HDGF, central system adult mice on cellular level by immunohistochemistry. In addition performed Western blot analysis various brain regions well neuronal glial cell cultures. was rather evenly throughout all tested with lowest substantia nigra. strongly thalamus, prefrontal parietal cortex, neurohypophysis, cerebellum, bulbus olfactorius, piriform cortex amygdala complex. were found be neurons, astrocytes oligodendrocytes. contrast, strong restricted except for weak oligodendrocytes stem. Although majority neurons positive, like cerebellar granule cells negative. The coexpression glia three many suggests different functions protein that might include proliferation survival. point special function this member cells.

参考文章(44)
Bernd Hamprecht, Fridolin Löffler, [27] Primary glial cultures as a model for studying hormone action Methods in Enzymology. ,vol. 109, pp. 341- 345 ,(1985) , 10.1016/0076-6879(85)09097-8
T. Kuroda, H. Yamamoto, T. Mori, T. Kishimoto, H. Nakamura, Y. Izumoto, K. Kawamura, H. Kambe, Molecular cloning of complementary DNA for a novel human hepatoma-derived growth factor. Its homology with high mobility group-1 protein. Journal of Biological Chemistry. ,vol. 269, pp. 25143- 25149 ,(1994) , 10.1016/S0021-9258(17)31509-0
Johannes Hirrlinger, Alexandra Resch, Jan Mirko Gutterer, Ralf Dringen, Oligodendroglial cells in culture effectively dispose of exogenous hydrogen peroxide: comparison with cultured neurones, astroglial and microglial cells. Journal of Neurochemistry. ,vol. 82, pp. 635- 644 ,(2002) , 10.1046/J.1471-4159.2002.00999.X
Tsung-Hui Hu, Chao-Cheng Huang, Li-Feng Liu, Pey-Ru Lin, Shang-Yun Liu, Hsueh-Wen Chang, Chi-Sin Changchien, Chuan-Mo Lee, Jiin-Haur Chuang, Ming Hong Tai, Expression of hepatoma-derived growth factor in hepatocellular carcinoma. Cancer. ,vol. 98, pp. 1444- 1456 ,(2003) , 10.1002/CNCR.11653
DT Nordquist, CA Kozak, HT Orr, cDNA cloning and characterization of three genes uniquely expressed in cerebellum by Purkinje neurons. The Journal of Neuroscience. ,vol. 8, pp. 4780- 4789 ,(1988) , 10.1523/JNEUROSCI.08-12-04780.1988
Peter Cherepanov, Eric Devroe, Pamela A. Silver, Alan Engelman, Identification of an evolutionarily conserved domain in human lens epithelium-derived growth factor/transcriptional co-activator p75 (LEDGF/p75) that binds HIV-1 integrase. Journal of Biological Chemistry. ,vol. 279, pp. 48883- 48892 ,(2004) , 10.1074/JBC.M406307200
Ralf Dringen, Lothar Kussmaul, Jan Mirko Gutterer, Johannes Hirrlinger, Bernd Hamprecht, The glutathione system of peroxide detoxification is less efficient in neurons than in astroglial cells. Journal of Neurochemistry. ,vol. 72, pp. 2523- 2530 ,(2002) , 10.1046/J.1471-4159.1999.0722523.X
Hirayuki Enomoto, Kenya Yoshida, Yoshihiko Kishima, Yorihide Okuda, Hideji Nakamura, Participation of hepatoma-derived growth factor in the regulation of fetal hepatocyte proliferation Journal of Gastroenterology. ,vol. 37, pp. 158- 161 ,(2002) , 10.1007/BF03326437
Nikolaus Machuy, Bernd Thiede, Krishnaraj Rajalingam, Christiane Dimmler, Oliver Thieck, Thomas F. Meyer, Thomas Rudel, A Global Approach Combining Proteome Analysis and Phenotypic Screening with RNA Interference Yields Novel Apoptosis Regulators Molecular & Cellular Proteomics. ,vol. 4, pp. 44- 55 ,(2005) , 10.1074/MCP.M400089-MCP200
Kazuhiro Ikegame, Mitsunari Yamamoto, Yoshihiko Kishima, Hirayuki Enomoto, Kenya Yoshida, Masaki Suemura, Tadamitsu Kishimoto, Hideji Nakamura, A new member of a hepatoma-derived growth factor gene family can translocate to the nucleus. Biochemical and Biophysical Research Communications. ,vol. 266, pp. 81- 87 ,(1999) , 10.1006/BBRC.1999.1733