TY - JOUR
T1 - Oxidized but not acetylated low-density lipoprotein reduces preproinsulin mRNA expression and secretion of insulin from HIT-T15 cells
AU - Okajima, Fumitaka
AU - Kurihara, Mikiko
AU - Ono, Chihaya
AU - Nakajima, Yasushi
AU - Tanimura, Kyoko
AU - Sugihara, Hitoshi
AU - Tatsuguchi, Atsushi
AU - Nakagawa, Kiyotaka
AU - Miyazawa, Teruo
AU - Oikawa, Shinichi
N1 - Funding Information:
This study was supported by Grants-in-Aid from the Japanese Ministry of Education, Science, Sport, and Culture #13671202 (to S.O), and in part by a Research Grant from Japan Foundation for Aging and Health, and by Health and Labour Sciences Research Grants from the Japanese Ministry of Health, Labor, and Welfare.
PY - 2005/2/21
Y1 - 2005/2/21
N2 - We examined the effect of oxidized low-density lipoprotein (oxLDL) on the insulin secretion in the culture of HIT-T15 cell line, an islet β-cell line derived from a hamster pancreatic tumor. In order to check the uptake of modified LDL by HIT-T15 cells, we prepared DiI-labeled native LDL (nLDL), acetylated LDL (AcLDL), and oxLDL. After the addition of each LDL into the cultures of HIT-T15 cells, fluorescence microscopic study was done. It was suggested that AcLDL and oxLDL were taken up by HIT-T15 cells, as well as nLDL. mRNA expression of the LDL receptor, CD36, and SR-B1 was detected in HIT-T15 by RT-PCR. The medium insulin level was measured in the culture of HIT-T15 cells with each LDL. oxLDL significantly reduced the insulin secretion stimulated by various concentrations of glucose, the intracellular content of insulin, and the expression of preproinsulin mRNA compared to the control cultures without LDL addition. In contrast, nLDL and AcLDL had no effect on the insulin secretion, the intracellular insulin level, or the expression of preproinsulin mRNA. MTT assay findings (reflecting cell numbers) were not different between cultures with and without LDLs. These results indicated that oxLDL disturbed the insulin metabolism of HIT-T15 cells.
AB - We examined the effect of oxidized low-density lipoprotein (oxLDL) on the insulin secretion in the culture of HIT-T15 cell line, an islet β-cell line derived from a hamster pancreatic tumor. In order to check the uptake of modified LDL by HIT-T15 cells, we prepared DiI-labeled native LDL (nLDL), acetylated LDL (AcLDL), and oxLDL. After the addition of each LDL into the cultures of HIT-T15 cells, fluorescence microscopic study was done. It was suggested that AcLDL and oxLDL were taken up by HIT-T15 cells, as well as nLDL. mRNA expression of the LDL receptor, CD36, and SR-B1 was detected in HIT-T15 by RT-PCR. The medium insulin level was measured in the culture of HIT-T15 cells with each LDL. oxLDL significantly reduced the insulin secretion stimulated by various concentrations of glucose, the intracellular content of insulin, and the expression of preproinsulin mRNA compared to the control cultures without LDL addition. In contrast, nLDL and AcLDL had no effect on the insulin secretion, the intracellular insulin level, or the expression of preproinsulin mRNA. MTT assay findings (reflecting cell numbers) were not different between cultures with and without LDLs. These results indicated that oxLDL disturbed the insulin metabolism of HIT-T15 cells.
KW - HIT-T15 cell
KW - Lipid peroxidation
KW - Oxidative stress
KW - Oxidized LDL
KW - Pancreatic beta cell
KW - Scavenger receptor
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U2 - 10.1016/j.bbalip.2004.11.018
DO - 10.1016/j.bbalip.2004.11.018
M3 - Article
C2 - 15708365
AN - SCOPUS:13644252970
SN - 1388-1981
VL - 1687
SP - 173
EP - 180
JO - BBA - Specialised Section On Lipids and Related Subjects
JF - BBA - Specialised Section On Lipids and Related Subjects
IS - 1-3
ER -