Expression of leptin receptor isoforms in rat brain microvessels

被引:258
|
作者
Bjorbæk, C
Elmquist, JK
Michl, P
Ahima, RS
van Bueren, A
McCall, AL
Flier, JS
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Dept Med,Sch Med, Div Endocrinol, Boston, MA 02215 USA
[2] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Dept Neurol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02215 USA
[4] Oregon Hlth & Sci Univ, Dept Vet Affairs Med Ctr, Div Endocrine, Med Serv, Portland, OR 97207 USA
[5] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97207 USA
[6] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97207 USA
关键词
D O I
10.1210/en.139.8.3485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Leptin acts on specific brain regions to affect body weight regulation. As leptin is made by white adipose tissue, it is thought that leptin must cross the blood-brain barrier or the blood-cerebrospinal fluid barrier to reach key sites of action within the brain. High expression of a short form leptin receptor has been reported in the choroid plexus. However, whether one or more of the known leptin receptor isoforms is expressed in brain capillaries is unknown. To identify and quantitate leptin receptor isoforms in rat brain microvessels, we applied quantitative RT-PCR to RNA from purified rat brain microvessels in parallel with in situ hybridization. The results show that the amount of short form leptin receptor messenger RNA (mRNA) in brain microvessels is extremely high, exceeding that in choroid plexus. In contrast, low levels of this mRNA were detected in the cerebellum, hypothalamus, and meninges. The long form leptin receptor mRNA is only present at low levels in the microvessels, but surprisingly, its level in cerebellum is 5 times higher than that in the hypothalamus. In situ hybridization experiments confirmed strong expression of short leptin receptors in microvessels, choroid plexus, and leptomeninges. The distribution and type of leptin receptor mRNA isoforms in brain microvessels are consistent with the possibility that receptor-mediated transport of leptin across the blood-brain barrier is mediated by the short leptin receptor isoform.
引用
收藏
页码:3485 / 3491
页数:7
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