Differential expression and regulatory roles of FABP5 and FABP7 in oligodendrocyte lineage cells

被引:0
作者
Kazem Sharifi
Majid Ebrahimi
Yoshiteru Kagawa
Ariful Islam
Tuerhong Tuerxun
Yuki Yasumoto
Tomonori Hara
Yui Yamamoto
Hirofumi Miyazaki
Nobuko Tokuda
Takeo Yoshikawa
Yuji Owada
机构
[1] Yamaguchi University Graduate School of Medicine,Department of Organ Anatomy
[2] RIKEN Brain Science Institute,Department of Molecular Psychiatry
来源
Cell and Tissue Research | 2013年 / 354卷
关键词
FABP; Oligodendrocyte progenitor cells; Oligodendrocyte; Proliferation; Differentiation;
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摘要
Fatty-acid-binding proteins (FABPs) are key intracellular molecules involved in the uptake, transportation and storage of fatty acids and in the mediation of signal transduction and gene transcription. However, little is known regarding their expression and function in the oligodendrocyte lineage. We evaluate the in vivo and in vitro expression of FABP5 and FABP7 in oligodendrocyte lineage cells in the cortex and corpus callosum of adult mice, mixed cortical culture and oligosphere culture by immunofluorescent counter-staining with major oligodendrocyte lineage markers. In all settings, FABP7 expression was detected in NG2+/PDGFRα+ oligodendrocyte progenitor cells (OPCs) that did not express FABP5. FABP5 was detected in mature CC1+/MBP+ oligodendrocytes that did not express FABP7. Analysis of cultured OPCs showed a significant decrease in the population of FABP7-knockout (KO) OPCs and their BrdU uptake compared with wild-type (WT) OPCs. Upon incubation of OPCs in oligodendrocyte differentiation medium, a significantly lower percentage of FABP7-KO OPCs differentiated into O4+ oligodendrocytes. The percentage of mature MBP+ oligodendrocytes relative to whole O4+/MBP+ oligodendrocytes was significantly lower in FABP7-KO and FABP5-KO than in WT cell populations. The percentage of terminally mature oligodendrocytes with membrane sheet morphology was significantly lower in FABP5-KO compared with WT cell populations. Thus, FABP7 and FABP5 are differentially expressed in oligodendrocyte lineage cells and regulate their proliferation and/or differentiation. Our findings suggest the involvement of FABP7 and FABP5 in the pathophysiology of demyelinating disorders, neuropsychiatric disorder and glioma, conditions in which OPCs/oligodendrocytes play central roles.
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页码:683 / 695
页数:12
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  • [1] Aberg K(2006)Human QKI, a potential regulator of mRNA expression of human oligodendrocyte-related genes involved in schizophrenia Proc Natl Acad Sci U S A 103 7482-7487
  • [2] Saetre P(2005)Brain lipid-binding protein is a direct target of Notch signaling in radial glial cells Genes Dev 19 1028-1033
  • [3] Jareborg N(2005)Role of Fabp7, a downstream gene of Pax6, in the maintenance of neuroepithelial cells during early embryonic development of the rat cortex J Neurosci 25 9752-9761
  • [4] Jazin E(2003)Dysregulated brain development in adult men with schizophrenia: a magnetic resonance imaging study Biol Psychiatry 53 412-421
  • [5] Anthony TE(2009)Peroxisome proliferator-activated receptor-gamma agonists promote differentiation and antioxidant defenses of oligodendrocyte progenitor cells J Neuropathol Exp Neurol 68 797-808
  • [6] Mason HA(1998)Structural evaluation of the prefrontal cortex in schizophrenia Am J Psychiatry 155 1049-1055
  • [7] Gridley T(2008)A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function J Neurosci 28 264-278
  • [8] Fishell G(1998)Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls Arch Gen Psychiatry 55 1084-1091
  • [9] Heintz N(2011)Peroxisome proliferator-activated receptor gamma agonists accelerate oligodendrocyte maturation and influence mitochondrial functions and oscillatory Ca(2+) waves J Neuropathol Exp Neurol 70 900-912
  • [10] Arai Y(2011)Regulating the balance between symmetric and asymmetric stem cell division in the developing brain Fly (Austin) 5 237-241