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Anat Cell Biol. 2010 September; 43(3): 194–200.
Published online 2010 September 30. doi:  10.5115/acb.2010.43.3.194
PMCID: PMC3015037

Ethanol down regulates the expression of myelin proteolipid protein in the rat hippocampus

Abstract

It is well known that chronic ethanol treatment affects the synthesis of RNA and protein in the brain and the maintenance and function of nervous system. The changes in myelination-related genes are most prominent in human alcoholics. Previously, our cDNA microarray study showed altered Proteolipid protein (PLP), a major protein of central myelin. The present study aimed to gain more understanding of the expression of PLP after chronic ethanol treatment. Male Sprague-Dawley rats were daily treated with ethanol (15% in saline, 3 g/kg, i.p.) or saline for 14 days. Messenger RNAs from hippocampus of each group were subjected to cDNA expression array hybridization to determine the differential gene expressions. Among many ethanol responsive genes, PLP was negatively regulated by ethanol treatment, which is one of the most abundant proteins in the CNS and has an important role in the stabilization of myelin sheath. Using northern blot and immunohistochemical analysis, we showed the change in expression level of PLP mRNA and protein after ethanol treatment. PLP mRNA and protein were decreased in hippocampus of rat with chronic ethanol exposure, suggesting that ethanol may affect the stabilization of myelin sheath through the modulation of PLP expression and induce the pathophysiology of alcoholic brain.

Keywords: rat, brain, hippocampus, alcohol, proteolipid protein

Introduction

Chronic ethanol consumption has adverse effects on the entire central nervous system (Ollat & Sebban, 1983; Deitrich et al., 1989; Samson & Harris, 1992). Previous studies have demonstrated that chronic ethanol intake induces alteration of brain functions, which may be caused by effects of ethanol on neuronal functions (Walker et al., 1980; Deitrich et al., 1989; Ryabinin 1998). Changes in neuronal functions caused by chronic exposure to ethanol are believed to underlie manifestations of a variety of psychiatric disorders and behavioral dysfunctions (Deitrich et al., 1989; Samson & Harris, 1992).

Recent study of gene expression monitoring with cDNA expression arrays provides a simple way to explore the biochemical effects of ethanol on the brain (Duggan et al., 1999; Bowers et al., 2006). The results of cDNA microarray studies showed that various genes related to oxidative stress and membrane trafficking were changed by chronic ethanol treatment. Also, these studies showed that ethanol interacts with various proteins and modifies protein function in the central nervous system (CNS) (Saito et al., 2002). Specially, the changes in myelination-related genes were most prominent in human alcoholics (Liu et al., 2004). One of the most abundant protein in mammalian CNS is Proteolipid protein (PLP), and PLP contributes to myelin's unique biological properties owing its high affinity to lipid (Boison et al., 1995; Möbius et al., 2008). Consistently, we detected PLP changes in our cDNA microarray study.

The aim of the present study is to investigate the changes in PLP mRNA and protein expression in the hippocampus of rat with prolonged ethanol treatment, which may have an important role in learning and memory.

Materials and Methods

Experimental animals

Male Sprague-Dawley rats were purchased from Samtaco Co. (Osan, South Korea) and were maintained in the animal facility at the Gyeongsang National University School of Medicine. Rats were treated in accordance with standard guidelines for laboratory animal care. All rats were provided standard chow and water ad libitum. Ethanol was diluted to 15% and given intraperitoneally at a dose of 3 g/kg b.w. in solution of 0.9% saline for 14 days. We used total 10 animals per group, 6 animals for extraction of RNA and 4 animals for tissue preparation. Control animals were injected with an equivalent volume of 0.9% saline. This dose resulted in blood ethanol levels that peak within 15 min of administration via either route (intraperitoneal, intragastric) and remain elevated for at least 3 hr.

cDNA expression array

Gene expression was analyzed using a cDNA expression array (Clontech laboratory, Palo, CA). Twenty µg of total RNA from hippocampus of saline- and ethanol-treated animals were reverse transcribed respectively. Solution containing hippocampal RNA, oligo (dT) primer, 0.5 µM dNTP (without dCTP), and reverse transcription buffer were heat-denatured at 65[degree celsius] for 10 min. 50 µCi of 32P-d CTP (3,000 Ci/mmol, NEN), 200 units of MMLV reverse transcriptase (Promega, Fitchburg, Wisconsin) and 20 units of RNasin were added and incubated at 37[degree celsius] for 1 hr. Free isotope was removed by Sephadex G-50 column chromatography (Pharmacia, Uppsala, Sweden). Radioactivity was checked by β-counter. Labelled probes were denatured by boiling for 10 min and added to hybridization solution containing 50% deionized formamide, 5X SSPE, 1X Denhardts solution, 0.1% SDS, and 2 mg of heat-denatured salmon sperm DNA, to reach a final probe concentration of 1×106 cpm/ml and freshly applied to the atlas cDNA expression array membrane, which was prehybridized in 20 ml of hybridization solution at 42[degree celsius] on a compact locker for 2 hr. Hybridization proceeded overnight at 42[degree celsius] on a compact locker. Following hybridization, membranes were stringently washed with agitation for 10 min in 200ml of prewarmed (42[degree celsius]) solution 1 (2X SSPE, 0.1% SDS) twice and solution 2 (0.1X SSPE, 0.1% SDS) twice at 42[degree celsius] for 5 min. Afterwards, membranes were exposed to X-ray film (Pharmacia, Uppsala, Sweden) at -70[degree celsius] for 3 days.

Tissue preparation

For in situ hybridization & immunohistochemistry, rats were anesthetized with pentobarbital sodium and perfused via the left cardiac ventricle with approximately 250~300 ml of 4% paraformaldehyde in 0.1 M Phosphate buffered saline after perfusion with 100~150 ml of 0.9% saline. Brains were quickly removed after perfusion and further fixed with the same fixative for 12 hr at 4[degree celsius], fixed brains were rinsed for 24 hr in 20% sucrose and sectioned serially at 12 µm thickness in a cryostat (Leica, Wetzlar, Germany) at -20 µm. Each section was then mounted on gelatin coated slides and stored at -70[degree celsius] until use. Since prolonged storage of tissue section seemed to decrease the intact mRNA, tissue section was used within 1 month. Solutions were prepared with DEPC-treated distilled water to further eliminate RNase contamination.

Northern blot analysis

Total RNAs were extracted by the acid guanidinium thiocyanate-phenol-chloroform method. The total RNAs (20 µg) separated by formaldehyde/1.2% agarose gel electrophoresis, transferred to a 0.45 µm Nytran membrane for 18~24 hr by diffusion blotting, then the RNA blotted membrane was UV-crosslinked. Prehybridization was carried out at 42[degree celsius] for 2 hr in a heat-sealable plastic bag (Invitrogen, Carlsbad, CA) with hybridization buffer consisting of 50% deionized formamide, 5X SSPE, 1X Denhardts solution, 0.1% SDS, and 2 mg of heat-denatured salmon sperm DNA. After addition of each 32P-labelled PLP cDNA probe as made by random primer labeling method. Hybridization was preformed at 42[degree celsius] for 24 hr. Following hybridization, the membrane was washed twice with 2x SSPE and 0.1% SDS at room temperature for 10 min, followed by the second washing with 0.07x SSPE, 0.5% SDS, and 5 mM EDTA (pH 8.0) at 42[degree celsius] for 5 min. The membrane was exposed to X-ray film (Fuji, Tokyo, Japan) at -70[degree celsius] for 3 days.

In situ hybridization

All solutions were made with sterile water, and glasswares were autoclaved to prevent contamination by RNase. The antisense PLP cRNA was transcribed in vitro from a vector containing a 238 bp fragment of the cloned rat cDNA using sp6 polymerase in the presence of 35S-UTP (1,250 ci/mmol, NEN). 35S-UTP labeled probes were prepared using in vitro transcription kit (Promega, Fitchburg, Wisconsin). Sections were dried, washed with 0.1 M Phosphate buffered saline, permeabilized by proteinase K, acetylated, and hybridized at 55[degree celsius] for 20 hr. The sections were then incubated with 50 µg/ml RNase A for 30 min at 37[degree celsius] and then washed with a series of SSC solutions. The highest stringency wash was 0.1 X SSC at 60[degree celsius] for 30 min, and dehydrated in alcohol solution with ascending concentration. Tissue Sections were coated with NTB2 emulsion (Invitrogen, Carlsbad, CA), kept at 4[degree celsius] for 14 days, and developed. Tissue sections were counterstained with cresyl violet. The slides were observed under a bright field microscopy, and then photographed.

Immunohistochemistry

For the localization of immunoreactive PLP, avidin-biotin complex (ABC) method was used. Tissue sections on slides were air-dried, dipped in 0.1 M PBS (pH 7.0) twice for 10 min, and rinsed with Triton X-100 in 0.1 M PBS for 10 min. Tissue sections were incubated with 50 µl of normal horse serum, diluted 1 : 100 for 30 min to exclude the nonspecific binding before the primary antibody application. Then slides were applied with 50 µl of the primary antibody, mouse-derived anti-PLP (Santa Cruz Biotechnology, CA) with a final dilution of 1 : 500 for overnight at 4[degree celsius]. Tissue sections were washed with 0.1 M PBS for 10 min twice, incubated with biotinylated secondary antibody (Santa Cruz Biotechnology, CA) for 2 hr at room temperature. After washing an excess secondary antiserum, ABC diluted 1 : 250 was treated for 2 hr at room temperature. Slides were washed again in PBS and Triton X-100, and then were rinsed with PBS for 10 min at room temperature. Slides were incubated in 0.05% 3,3'-diaminobenzidine tetrahydrochloride (DAB) in PBS for 10 min. Hydrogen peroxide was added to the same DAB solution to make a final concentration of 0.01% H2O2, and the container was shaken gently as the reaction proceeded. After 1~2 min, as determined by the degree of staining with the light microscope, the reaction was terminated with several washes of PBS. Tissue sections were observed under a light microscopy and photographed.

Results

To examine the effects of ethanol on PLP expression in the hippocampus, we performed cDNA microarray in SD rats, and found that PLP was reduced approximately ~36% (Fig. 1). In order to confirm the reduced expression of PLP by ethanol using array hybridization, total RNAs were extracted from hippocampus and subjected to northern blot analysis with GAPDH as internal standard (Fig. 2). Quantification of PLP mRNA northern blot analysis showed that PLP mRNA was decreased approximately ~30% in the hippocampus of ethanol-treated rats compared with control and this result was consistent with cDNA array.

Fig. 1
Expression array hybridized with 32P-labeled cDNA from hippocampal pools of control saline- and ethanol-treated animals as revealed with X-ray film (upper panel) exposed for 3 days. The cDNAs on the bottom line of upper panel are commonly considered as ...
Fig. 2
Northern blot analysis of PLP mRNA. Twenty µg of total RNA from hippocampus of saline- or ethanol-treated rats were electrophoresed formaldehyde contained 1.2% agarose gel and transferred to nytran membrane, then hybridized with 32P-labeled gene ...

To evaluate the localization and expressional changes of PLP mRNA in the hippocampal region, in situ hybridization was applied. PLP mRNA was observed in the hippocampus proper (stratum radiatum layer) where the axons, from pyramidal cell and inter neuronal dendrite, form network (Fig. 3). Higher magnification view of PLP in saline treated group (Fig. 3B) showed some cells have dense signals but not in the same area of ethanol-treated group (Fig. 3D). Since PLP is the main protein of CNS myelin and myelin sheaths are formed by oligodendrocyte (Boison et al., 1994; Sarret et al., 2010), those cells may be oligodendrocytes. As well, PLP is known to colocalize with myelin basic protein , supporting our results (Boison et al., 1995).

Fig. 3
Bright field photomicrography of PLP mRNAs in the hippocampus of control saline- (A, B) and ethanol-treated animals (C, D). PLP mRNAs were localized in the brain slice (12 µm in thickness) at the level of 3.0 mm post bregma using in situ hybridization ...

It was clearly confirmed that the levels of PLP mRNA expression decreased in the hippocampus of ethanol-treated rats using northern blot analysis, and in situ hybridization.

Then, we examined whether ethanol affects PLP using immunohistochemical analysis. We found that PLP in the hippocampus from ethanol-treated rats was reduced in the hippocampus stratum radiatum layer compared with control (Fig. 4).

Fig. 4
Immunohistochemical detection of myelin PLP in the rat hippocampus from saline- (A, B) and ethanol-treated rats (C, D). Clear-cut decreases in PLP immunoreactivities were observed in the ethanol-treated hippocampal regions. Scale bars=A and C, 1,000 µm; ...

Discussion

In the present study, we found that PLP mRNA and its protein expression was reduced in the hippocampus of rats with prolonged ethanol administration. This result augmented that hippocampus is one of the brain regions most sensitive to prolonged ethanol administration and suggested that chronic ethanol administration may interfere normal function of hippocampus primarily via down-regulating the PLP mRNA and its protein expression.

In CNS, myelin is a modified form of the oligodendroglial plasma membrane, and spiraled around the axon extending to form a multilamellar structure. The compaction of myelin is essential for neuronal function, and it involves the close apposition of the cytoplasmic and extracellular surfaces of plasma membrane from specialized glial cells to form the major dense line (MDL) and the intraperiod line (IPL), respectively (Inoue et al., 1973; Peters et al., 1991). The myelin PLP is a main component of intraperiod lines and its function is to assemble myelin lamellae (Boison & Stoffel, 1994; Boison et al., 1995). Although the full array of biological functions of the myelin proteolipid has not yet been clearly defined, PLP appears to be important to stabilize the myelin sheath and maintain the structural integrity of the myelin membrane (Duncan et al., 1987; Boison & Stoffel, 1994).

Myelination of nerve fibers is essential for the function of the vertebrate nervous system. Myelination in the brain has been an area of interest in human alcohol studies due to the observed brain damage in alcoholics and the potential role of demyelination in this process (Kril & Halliday, 1999; Lewohl et al., 2001). It was reported that myelin-related genes, myelin basic protein (MBP), myelin proteolipid protein (PLP) and myelin oligodendrocytes glycoprotein (MOG) were down-regulated in the frontal cortex of human alcoholics (Liu et al., 2004). Also, the compaction of myelin enlamellate in the CNS of PLP-null mice was incompleted (Rosenbluth et al., 2006).

A series of mutant animals lacking PLP (Boison et al., 1995; Rosenbluth et al., 1996; Klugmann et al., 1997) as well as several human disorders involving the PLP gene (Griffiths et al., 1998; Daigo et al., 2008; Tanaka et al., 2009) display severe neurological impairment, emphasizing the physiological importance of this protein in nervous system. In the absence of myelin sheath, as seen in demyelization diseases, impulse conduction is impeded resulting in severe sensory and motor deficits (Boison & Stoffel, 1994).

Although PLP expression and its function in the cortex and cerebellum were widely studied in human alcoholics and murine alcohol model, PLP in the hippocampus remains to be explored. In the present study, we showed the expression of PLP mRNA and its protein were reduced in the hippocampus of rats with chronic ethanol treatment. More research is needed to elucidate the exact mechanism of deleterious effects of ethanol on the hippocampus, but one possible scenario is that prolonged ethanol exposure may interfere the normal function of hippocampal neurons by down-regulating the PLP expression.

Acknowledgments

This work was supported by the National Research Foundation of Korea (NRF) (No. R13-2005-012-01001-0).

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