Cerebral Apolipoprotein D Exits the Brain and Accumulates in Peripheral Tissues

被引:7
作者
Desmarais, Frederik [1 ,2 ]
Herve, Vincent [2 ,3 ]
Bergeron, Karl F. [1 ]
Ravaut, Gaetan [1 ]
Perrotte, Morgane [3 ]
Fyfe-Desmarais, Guillaume [1 ,2 ]
Rassart, Eric [2 ]
Ramassamy, Charles [3 ]
Mounier, Catherine [1 ]
机构
[1] Univ Quebec Montreal UQAM, Dept Sci Biol, Ctr Rech CERMO FC, Lab Metab Mol Lipides, 141 Av President Kennedy, Montreal, PQ H2X 1Y4, Canada
[2] Univ Quebec Montreal UQAM, Dept Sci Biol, Lab Biol Mol, 141 Av President Kennedy, Montreal, PQ H2X 1Y4, Canada
[3] Inst Natl Rech Sci INRS, Ctr Armand Frappier Sante Biotechnol, 531 Boul Prairies, Laval, PQ H7V 1B7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
apolipoprotein D; basigin; protein accumulation; blood-brain barrier;
D O I
10.3390/ijms22084118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apolipoprotein D (ApoD) is a secreted lipocalin associated with neuroprotection and lipid metabolism. In rodent, the bulk of its expression occurs in the central nervous system. Despite this, ApoD has profound effects in peripheral tissues, indicating that neural ApoD may reach peripheral organs. We endeavor to determine if cerebral ApoD can reach the circulation and accumulate in peripheral tissues. Three hours was necessary for over 40% of all the radiolabeled human ApoD (hApoD), injected bilaterally, to exit the central nervous system (CNS). Once in circulation, hApoD accumulates mostly in the kidneys/urine, liver, and muscles. Accumulation specificity of hApoD in these tissues was strongly correlated with the expression of lowly glycosylated basigin (BSG, CD147). hApoD was observed to pass through bEnd.3 blood brain barrier endothelial cells monolayers. However, cyclophilin A did not impact hApoD internalization rates in bEnd.3, indicating that ApoD exit from the brain is either independent of BSG or relies on additional cell types. Overall, our data showed that ApoD can quickly and efficiently exit the CNS and reach the liver and kidneys/urine, organs linked to the recycling and excretion of lipids and toxins. This indicated that cerebral overexpression during neurodegenerative episodes may serve to evacuate neurotoxic ApoD ligands from the CNS.
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页数:18
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