Aromatase immunoreactivity in fetal ovine neuronal cell cultures exposed to oxidative injury.

A lot of evidence testifies that aromatase is expressed in the central nervous system where it has been detected not only in hypothalamic and limbic regions but also in the cerebral cortex and spinal cord. In physiological conditions, aromatase is expressed exclusively by neurons, where it has been mainly found in cell bodies, processes and synaptic terminals. Moreover, primary cultured cortical astrocytes from female rats are more resistant to oxidant cell death than those from males, suggesting a protective role of estradiol. The aim of this study was to evaluate changes in aromatase expression in response to 3-nitro-L-tyrosine, a marker of oxidative stress, in primary neuronal cell cultures from brains of 60-day old sheep fetuses. Cells were identified as neurons by using class III β-tubulin, a marker of neuronal cells. Two morphological types were consistently recognizable: i) bipolar cells with an oval cell body; ii) multipolar cells whose processes formed a wide net with those of adjacent cells. In situ hybridization technique performed on 60-day old fetal neurons revealed that in baseline conditions aromatase gene expression occurs. Importantly, cells exposed to 360 µM 3-nitro-L-tyrosine were fewer and showed more globular shape and shorter cytoplasmic processes in comparison to control cells. The immunocytochemical study with anti-aromatase antibody revealed that cells exposed to 360 µM 3-nitro-L-tyrosine were significantly more immunoreactive than control cells. Thus, it can be postulated that the oxidant effects of the amino acid analogue 3-nitro-L-tyrosine could be counterbalanced by an increase in aromatase expression that in turn can lead to the formation of neuroprotective estradiol via aromatization of testosterone.

The brain is an important site of steroid synthesis in vertebrates (Baulieu, 1997). Neuroendocrine tissue is capable of converting androgens into estrogens by the enzyme P450 aromatase (Naftolin ). Estradiol, through its specific receptors, promotes many crucial regulatory effects on various processes, such as viability and survival of neurons in rat primary cultures (Chowen ), neural differentiation and plasticity as well as sexual behavior. Aromatase modulates synaptic plasticity in the hippocampus and other brain regions related to cognition.The enzyme may also influence synaptic development and plasticity in other non-reproductive regions of the central nervous system. For instance, Purkinje cells in aromatase-knockout mice show decreased dendritic growth and impairment of formation of dendritic spines and synapses (Sasahara ). In addition, numerous studies have shown expression, activity and distribution of aromatase in the central nervous system of rats (Shinoda ) and humans (Yague ). In the brain, aromatase is predominantly expressed in hypothalamic and limbic regions, but also other structures such as the cerebral cortex, midbrain and spinal cord reveal aromatase activity and immunoreactivity.

It has been demonstrated that aromatase is neuroprotective in the central nervous system. For instance, treatment with the neurotoxin kainic acid resulted in significant neuronal loss in the hippocampus of rats treated with the aromatase inhibitor fadrozole (Azcoitia ). Under baseline conditions, aromatase is expressed in the central nervous system of mammals exclusively by neurons, where it has been mainly found in cell bodies, processes and synaptic terminals (Naftolin ). Since aromatase is expressed in several cellular compartments, it can be supposed that it leads to the formation of estrogen that acts not only through the classical receptors but also by direct and rapid effects at neuronal membranes (Roselli, 2007).

Aromatase-expressing astrocytes have been observed in rats after stressful conditions such as serum deprivation or ischemia (Azcoitia , Roselli, 2007). The increased expression of aromatase in injured brain areas suggests that the enzyme may be involved in the protection of nervous tissue by increasing levels of local estrogens. Moreover, primary cultured cortical astrocytes from female rats are more resistant to oxidant cell death than males, suggesting estradiol has a protective role (Liu ). In particular, these Authors demonstrated that astrocytes isolated from neonatal cortex exhibit marked sex differences in the sensitivity to oxygen-glucose deprivation and oxidant cell death since female cells exhibited enhanced aromatization and estradiol formation.

The present investigation describes for the first time changes in aromatase expression in response to 3-nitro-L-tyrosine - a marker of oxidative stress - in primary neuronal cultures from fetal sheep brain.

Materials and Methods

Cells derived from the brains of twelve 60-day old sheep fetuses were obtained from local abbatoirs when pregnant sheep were slaughtered. The period of gestation was established measuring fetal crown-rump length, following the tables reported by McGeady . One fragment from each brain was suspended in ice-cold cell freezing medium composed of Dulbecco’s modified Eagle’s medium (DMEM) with 1% HEPES (pH 7.4), 10% fetal calf serum and 10% dimethylsulfoxide (DMSO), following the cryopreservation method reported for neural tissue of bovine species (Hashimoto ). Cryotubes were slowly cooled to −80°C and transferred to liquid nitrogen the following day. Frozen tissues were rapidly thawed in a water bath at 38°C and minced in small fragments under sterile conditions. A papain dissociation system kit (Worthington Biochemical Corporation, Lakewood, NJ, USA) was used to dissociate cells. Cells were then suspended in a basal medium for cell culture consisting of a 1:1 mixture of DMEM and Ham’s F12, supplemented with penicillin (30 mg/L), streptomycin (50 mg/L), sodium bicarbonate (2.4 g/L), insulin (10 µg/mL), transferrin (10 µg/mL), sodium selenite (10−8M) and 10% fetal calf serum, at 38°C in a 5% CO2 humidified atmosphere. Cells were plated on glass coverslips, previously coated with poly-L-lysine (Sigma, St. Louis, MO, USA). Twenty coverslips from each fetal brain were obtained.

One monolayer per brain was used to characterize neurons by the immunofluorescence method. Briefly, at day 10 of culture, cells were fixed with 4% paraformaldehyde at room temperature for 30 min. After fixation, cells were washed with PBS, then permeabilized with 0.1% Triton X-100 for 15 min at room temperature and incubated overnight with a monoclonal antibody anti-class III β-tubulin (Sigma), a widely-recognized marker of neuronal cells, diluted 1:200. Cells were then incubated for 1h at 37°C with the antimouse FITC-conjugated antibody (Sigma) diluted 1:100. In addition, nuclei were counterstained with Hoechst #33258 fluorescent dye. One additional monolayer per brain was used as negative control by omitting the primary antibody or employing non-immune mouse serum. Cells were finally examined by confocal microscopy.

In order to detect aromatase gene expression in baseline conditions, in situ hybridization technique was performed. A melting curve ranging 37° to 42°C was performed in a preliminary study carried out at our labs, indicating 38°C as the optimal temperature. On one monolayer per brain biotinylated cDNA probe with a 48-nucleotide sequence from Sigma was pipetted and followed by incubation with streptavidin peroxidase complex and diaminobenzidine as chromogen. A second monolayer was incubated with sense probe and displayed no signal.

In addition, 5 monolayers per brain underwent 72 hr-exposure to 180 (2 coverslips) and 360 µM (3 coverslips) 3-nitro-L-tyrosine. Aromatase immunoreactivity was then detected by immunoperoxidase technique. The concentration of 180 and 360 µM 3-nitro-L-tyrosine were chosen as they were able to determine morphological alterations in C1300 murine neuroblastoma cell line (Zedda ).

In detail, cells were blocked for 20min with normal goat serum and incubated overnight at 4°C with a polyclonal anti-aromatase antibody obtained from rabbit (5 µg/mL, Acris, Hiddenhausen, Germany) diluted 1:200, then for 1h in biotinylated goat anti-rabbit antibody (Vector, Burlingame, CA, USA) diluted 1:250. This antibody recognises aromatase from numerous Mammalian species including bovine and sheep, as specified by Acris. After several rinses in PBS, sections were incubated with avidin-biotin complex system (ABC, Vector) for 30 min. Coverslips were then incubated with diaminobenzidine (DAB) for 1–5 min and finally dehydrated and mounted on slides. A second polyclonal antibody from Sigma confirmed the results. Both antibodies were preliminarily tested with Western blot using fetal sheep brain.

Five additional monolayers per brain underwent the protocol above without 3-nitro-L-tyrosine and served as controls. Quantitative analysis of immunocytochemical results was performed by means of Image J 1.42q software (NIH, Bethesda MD, USA) which detects variations of staining between 360 µM 3-nitro-L-tyrosine-treated and untreated cells. Averages ±SD from the data obtained are reported in the diagram in Figure 6.

Figure 6

Significant difference in the number of aromatase-immunopositive cells in 360 µM 3-nitro-L-tyrosine-exposed cultures and controls expressed in percentage, p<0.5.

A further six monolayers per sample, namely three cultured under baseline conditions and three after 72hr-360 µM 3-nitro-L-tyrosine exposure, were used to carry out viability assay with a mixture of Hoechst #33258 and propidium iodide dyes and observed by confocal microscope.

Results

In the living state and baseline conditions cells were numerous and viable and they grew to and adhered well on glass coverslips.Their cell bodies were spindle-like, oval- or triangular-shaped with long processes that tended to have contacts with those of the contiguous cells (Figure 1). The immunofluorescence method revealed that more than 90% of cultured cells could be identified as neurons, since they were class III β-tubulin positive. Two types of cells were detected: i) bipolar cells with an oval cell body and two long processes that originated from the opposite poles; ii) multipolar cells whose processes formed a wide net with those of adjacent cells (Figure 2). In situ hybridization technique showed that at gestation day 60, aromatase was expressed in fetal sheep brain, as shown in Figure 3. Treatment with 180 µM 3-nitro-L-tyrosine (Figure 4B) did not determine any significant change in cell number and morphology in comparison with controls (Figure 4A). In contrast, cells exposed to 360 µM 3-nitro-L-tyrosine (Figure 4C) were reduced in number and showed a more globular shape and shorter cytoplasmic processes in comparison to control cells. In addition, 360 µM 3-nitro-L-tyrosine-exposed cells displayed intracytoplasmic vacuols as a consequence of cell suffering (Figure 4D).

Figure 1

Phase contrast optics. Cells from 60-day old sheep fetuses. Cells are numerous and viable, oval- or triangular-shaped with long processes that tend to have contacts with those of the contiguous cells. Scale bar: 80 µm.

Figure 2

Confocal laser scanning microscopy. Most cells are positive to neuron-specific class III β-tubulin and show bipolar (arrow) and multipolar (arrowhead) shape as well as long cytoplasmic processes forming a wide net. Scale bar: 40 µm.

Figure 3

In situ hybridization study shows that aromatase is expressed in cultured cells at gestation day 60 and in baseline conditions. Scale bar: 40 µm.

Figure 4

Phase contrast optics. Cells exposed to 180µM 3-nitro-L-tyrosine (B) do not show any significant change in cell number and morphology in comparison with controls (A). Cells exposed to 360µM 3-nitro-L-tyrosine (C) show globular shape, short cytoplasmic processes and intracytoplasmic vacuols as a consequence of cell suffering (D). Scale bars in A, B: 80µm; C, D: 40µm.

The immunocytochemical method with anti-aromatase antibody revealed that cells exposed to 360 µM 3-nitro-L-tyrosine were significantly more immunoreactive than control cells (Figure 5). Although aromatase immunoreactivity was mainly detected in cell bodies, few cells displayed immunostained cytoplasmic processes as well. The quantitative analysis of anti-aromatase immunocytochemical results reported in the diagram of Figure 6 indicates statistically significant differences between percentages of stained cells in 360 µM 3-nitro-L-tyrosine-treated and untreated cultures.

Figure 5

Immunocytochemical study. Cells exposed to 360 µM 3-nitro-L-tyrosine (B) exhibit a higher aromatase immunoreactivity than control cells (A). Note that aromatase immunoreactivity is mainly confined to the cell body. Scale bar: 100 µm.

Finally, cell viability assay did not show any significant difference between controls and 72hr-360 µM 3-nitro-L-tyrosine-exposed monolayers.

Discussion

The present work shows for the first time changes in aromatase expression in response to 3-nitro-L-tyrosine, a marker of oxidative stress, in primary neuronal cultures from fetal sheep brain. In this study a relatively simple method to obtain pure cell cultures from fetal sheep brain is presented. This method is based on what reported by Peruffo who describe a protocol of obtaining primary cultures from the cerebral cortex and hypothalamus of bovine fetuses. According to these Authors, successful outcomes may depend on the brain region of cell collection, developmental stage and culture medium conditions. Such parameters are indeed capable of influencing cell differentiation, as well as the ratio between neurons and glial cells. Explants from cortex at early stages (10th week of pregnancy) yielded maximum amounts of neurons. In agreement with their reports, numerous and viable cells that grew to and adhered well on glass coverslips could be obtained in our study from the brain cortex and at early stage of sheep pregnancy (60th day). In such conditions, about 90% of growing cells were neurons (Peruffo ).

In our work, more than 90% of cultured cells were class III β-tubulin positive with bipolar and multipolar shape and long cytoplasmic processes forming a wide net. In this case, sheep cells behave like amphibian neurons where class III β-tubulin immunoreactivity is accompanied by the differentiation of cytoplasmic processes (Moody ). Our data are consistent with the report of Kay , who set up cortical and cerebellar neurons from 9 to 15-week old fetal sheep brains. Nearly all the cells cultured by these Authors from the youngest fetuses (9 weeks old) adhered as neurons. According to these Authors, the proportion of glial cells increased with age, as well as the risk of cultures of being overtaken by glial cells.

In our study, cells from fetuses at gestation day 60 and under baseline conditions express aromatase as revealed by in situ hybridization technique. This datum is in agreement with previous studies demonstrating the presence of aromatase activity in neurons obtained from hypothalamus of 14–15 day-old rat embryos (Negri Cesi ), as well as in diverse brain regions such as the hippocampus (Yague ). Cells exposed to 360 µM 3-nitro-L-tyrosine exhibited morphological changes as they became globular-shaped and reduced their cytoplasmic processes. This could be due to the action of 3-nitro-L-tyrosine on microtubules. Indeed, a previous work of ours showed that cell lines of neuronal and glial origin exposed to 360 µM 3-nitro-L -tyrosine underwent morphological changes and nuclear suffering as a result of nitrotyrosination of α-tubulin and consequent impairment of microtubular network (Zedda ).

It is of interest that the treatment of cells with 3-nitro-L-tyrosine resulted in a higher aromatase immunoreactivity than control cells. The oxidant action of the amino acid analogue 3-nitro-L-tyrosine could be counterbalanced by an increase in aromatase expression that in turn can lead to the formation of neuroprotective estradiol via aromatization of testosterone. Indeed, the neuroprotective properties of estradiol have been well documented (Behl, 2002) and a greater resistance against oxidant injury has been detected in female rat astrocytes than in males (Liu ).

In conclusion, our in vitro model could be useful to study the variations in aromatase expression in cells of neural origin and may contribute to a better understanding of some mechanisms of neurodegenerative disorders in which estrogens play a crucial role as antioxidant agents.