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A spontaneously immortalized Schwann cell line from aldose reductase‐deficient mice as a useful tool for studying polyol pathway and aldehyde metabolism
Author(s) -
Niimi Naoko,
Yako Hideji,
Takaku Shizuka,
Kato Hiroshi,
Matsumoto Takafumi,
Nishito Yasumasa,
Watabe Kazuhiko,
Ogasawara Saori,
Mizukami Hiroki,
Yagihashi Soroku,
Chung Sookja K.,
Sango Kazunori
Publication year - 2018
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/jnc.14277
Subject(s) - polyol pathway , schwann cell , immortalised cell line , aldehyde dehydrogenase , biology , aldose reductase , microbiology and biotechnology , cell culture , neurite , 4 hydroxynonenal , cell , biochemistry , enzyme , in vitro , genetics , lipid peroxidation
The increased glucose flux into the polyol pathway via aldose reductase ( AR ) is recognized as a major contributing factor for the pathogenesis of diabetic neuropathy, whereas little is known about the functional significance of AR in the peripheral nervous system. Spontaneously immortalized Schwann cell lines established from long‐term cultures of AR ‐deficient and normal C57 BL /6 mouse dorsal root ganglia and peripheral nerves can be useful tools for studying the physiological and pathological roles of AR . These cell lines, designated as immortalized knockout AR Schwann cells 1 ( IKARS 1) and 1970C3, respectively, demonstrated distinctive Schwann cell phenotypes, such as spindle‐shaped morphology and immunoreactivity to S100, p75 neurotrophin receptor, and vimentin, and extracellular release of neurotrophic factors. Conditioned media obtained from these cells promoted neuronal survival and neurite outgrowth of cultured adult mouse dorsal root ganglia neurons. Microarray and real‐time RT ‐ PCR analyses revealed significantly down‐regulated mRNA expression of polyol pathway‐related enzymes, sorbitol dehydrogenase and ketohexokinase, in IKARS 1 cells compared with those in 1970C3 cells. In contrast, significantly up‐regulated mRNA expression of aldo‐keto reductases ( AKR 1B7 and AKR 1B8) and aldehyde dehydrogenases ( ALDH 1L2, ALDH 5A1, and ALDH 7A1) was detected in IKARS 1 cells compared with 1970C3 cells. Exposure to reactive aldehydes (3‐deoxyglucosone, methylglyoxal, and 4‐hydroxynonenal) significantly up‐regulated the mRNA expression of AKR 1B7 and AKR 1B8 in IKARS 1 cells, but not in 1970C3 cells. Because no significant differences in viability between these two cell lines after exposure to these aldehydes were observed, it can be assumed that the aldehyde detoxification is taken over by AKR 1B7 and AKR 1B8 in the absence of AR.