Low Intraprostatic DHT Promotes the Infiltration of CD8+ T Cells in BPH Tissues <i>via</i> Modulation of CCL5 Secretion

Fan, Yu; Hu, Shuai; Liu, Jie; Xiao, Fei; Li, Xin; Yu, Wei; Cui, Yun; Sun, Mengkui; Lv, Tianjing; He, Qun; Jin, Jie

doi:https://doi.org/10.1155/2014/397815

Mediators of Inflammation

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Abstract Introduction Materials and Methods Results Discussion Acknowledgments References Copyright Related Articles

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Immune-Endocrine Cross-Talk in Reproductive Biology and Pathology

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Clinical Study | Open Access

Volume 2014 | Article ID 397815 | https://doi.org/10.1155/2014/397815

Low Intraprostatic DHT Promotes the Infiltration of CD8+ T Cells in BPH Tissues via Modulation of CCL5 Secretion

Yu Fan,^1,2Shuai Hu,^1,2Jie Liu,^1,2Fei Xiao,³Xin Li,^1,2Wei Yu,^1,2Yun Cui,^1,2Mengkui Sun,^1,2Tianjing Lv,^1,2Qun He,^1,2and Jie Jin^1,2

Academic Editor: Izabela Woclawek-Potocka

Received24 Dec 2013

Revised18 Feb 2014

Accepted26 Feb 2014

Published06 Apr 2014

Abstract

Clinical studies suggested thatandrogen might be associated with infiltrating T cells in prostate of benign prostatic hyperplasia (BPH) patients, but detail of T-cell subset and mechanism still remained unclear. The present study tested the hypothesis that intraprostatic 5α-dihydrotestosterone (DHT) exerts effects on T cells recruitment by BPH epithelial cells. Prostate tissues from 64 cases of BPH patients after transurethral resection of prostate (TURP) were divided into 2 groups: (1) no medication history; (2) administration of 5α-reductase type II inhibitor-finasteride 5 mg daily for at least 6 months before surgery. Group 2 presented significantly higher CD8+ T cells infiltration than group 1, but no changes in CD4+ T cells (immunohistochemistry and flow cytometry). In vitro study more CD8+ T cell migrated to the prostate tissue lysates from group 2 and BPH-1 cells in low DHT condition. Transcription of chemokine (C-C motif) Ligand 5 (CCL5) mRNA in BPH-1 cells and chemokine (C-C motif) receptor 5 (CCR5) mRNA in CD8+ T cells were upregulated in low DHT condition (q-PCR). CCL5 expression was also identified to be higher in group 2 prostate tissues by IHC. This study suggested that intraprostatic DHT may participate in regulating inflammatory response which was induced by human prostatic epithelial cell, via modulating CCL5 secretion.

1. Introduction

Benign prostatic hyperplasia (BPH) is one of the most common chronic diseases in aging men [1]. The most potent androgen in men, 5α-dihydrotestosterone (DHT), is widely accepted to be more essential than testosterone for prostatic epithelial cell proliferation and function [2]. It is believed to be largely converted from testosterone in prostate by the action of 5α-reductase enzyme [3]. So the mainstay of therapies is the 5α-reductase inhibitors, which regulate the levels of intraprostatic DHT. Finasteride, a competitive inhibitor of 5α-reductase-type II with relatively low affinity for type I [4], has been one of the most commonly prescribed drugs for the management of BPH. It markedly reduces intraprostatic DHT concentration [5]. 5α-reductase inhibitors (finasteride) exert a strong apoptotic effect on the DHT-dependent epithelium, but in some BPH patients finasteride fails to control symptoms.

To date, chronic inflammation has been recognized as another key player in the BPH pathogenesis and progression [6]. Meanwhile, many studies have showed that the majority of lymphocytes in BPH tissue were T-lymphocytes [7, 8]; infiltration of chronically T lymphocytes and secretion of inflammatory cytokines with the prostatic gland are considered a determinant factor in BPH pathogenesis and progression [9]. Unfortunately, most of the recent studies focused on the proinflammatory cytokines secreted by T-lymphocytes and BPH cells [10]. The causes for T-cell infiltration and immune dysregulation in the prostate remain subjects of debate.

The most important potential cause for immune response in prostate is the prostatic microenvironment [11]. BPH epithelial cells, an important component of prostatic microenvironment, are suggested as a key role of the induction of immune-mediated inflammatory processes [12]. On the other hand, intraprostatic DHT could affect function of epithelial cell directly [13]. Accordingly, it suggests some linkages between inflammation and intraprostatic DHT. Vignozzi et al. (2012) [14] reported that intraprostatic testosterone plays a protective role in metabolic syndrome-associated prostate inflammation in rabbit model. From a pathophysiological standpoint, some studies showed correlation between DHT level and inflammation [15], but the detail of T cell subsets infiltration influenced by BPH epithelial cells and intraprostatic DHT still remained largely unresolved.

In the present work, we focused on the relationship between intraprostatic DHT level, BPH epithelial cells, and T-cell infiltration. We further elucidated the chemokine changes in different level of intraprostatic DHT.

2. Materials and Methods

2.1. Materials

2.1.1. Patients

The patients were selected by considering medication duration from the medical records of 726 patients who underwent transurethral resection of the prostate (TURP) between January 2008 and December 2011 in Peking University First Hospital. According to the medication history, prostate tissue was obtained from 64 prostatic hyperplasia patients by transurethral resection. Patients were divided into two groups: group 1 consisted of 28 patients who had been medicated neither with α-adrenergic blocker nor with 5α-reductase inhibitor; group 2 consisted of 36 patients treated with finasteride 5 mg daily for longer than six months before surgery. All included samples were pathologically confirmed as benign prostatic hyperplasia without prostate cancer or prostatic intraepithelial neoplasia (PIN). And the patients who had urinary tract infection or previous prostate-related surgery or were treated with urinary catheter were excluded from the study.

2.1.2. Reagents and Antibodies

Monoclonal anti-CCL5 antibodies and the recombinant protein IgG were purchased from R&D systems (MAB678, MAB002, Minneapolis, MN, USA), and 500 μg/mL stock was reconstituted in phosphate buffered saline (PBS). For anti-CCL5 treatment, stocks were adjusted to a final concentration of 6 μg/mL. Ficoll-Paque was purchased from Amersham Pharmacia Biotech (17144002, Piscataway, NJ, USA). Collagenase D was purchased from Roche Diagnostic (100 mg, 11088858001 Indianapolis, IN, USA) and was adjusted to a final concentration of 1 mg/mL to use. Antibodies used for flow cytometry included PE-Cy 7-conjugated mouse anti-human CD3 antibody (341091), fluorescein isothiocyanate (FITC)-conjugated mouse anti-human CD4 antibody (340133), phycoerythrin (PE)-conjugated mouse anti-human CD8 antibody (340046), PE-Cy 7-conjugated mouse IgG1, κ isotype (555872), FITC-conjugated mouse IgG1 κ isotype (555909), or PE-conjugated mouse IgG1κ isotype (554680). All these FACs antibodies were purchased from BD Biosciences (NJ, USA). Antibodies used for immunohistochemistry included Rabbit anti-CD4(+) (dilution 1 : 50, ab133616, Abcam, Cambridge, UK), anti-CD8(+) (dilution 1 : 50, RM-9116-S1, Thermo Fisher Scientific, Cheshire, UK), and the rabbit anti-CCL5 (+) (2 μg/mL, ab9679, Abcam, Cambridge, UK).

2.2. Experimental Procedures

2.2.1. Blood Sample Preparation

Blood samples were collected in sterile heparinized containers from 6 health persons at 10 mL per tube. Purification of human Peripheral blood mononuclear cells was performed according to some previous publications [16]. Peripheral blood mononuclear cells (PBMC) were isolated by Ficoll density gradient and blood was centrifuged for 20 min at 2000 ×g. The cells were washed twice in phosphate buffered saline (PBS, pH 7.2) without calcium and magnesium and resuspended in X-VIVO 15 medium (04-418Q, Lonza, NJ, USA) for further analysis.

2.2.2. Prostate Tissue Preparation

Prostate tissue preparation was performed as the publication description [17]. One part of fresh prostate tissue which was got from surgery was placed in a solution of 1 mg/mL Collagenase D (Roche) in RPMI 1640 media containing 10% FBS with DNase I (20 μg/mL; Sigma-Aldrich, St. Louis, MO, USA). Tissue was minced at about 1 mm³ and placed at 37°C for 1 hr for digestion, followed by passing through a 70 μm filter. Then the lymphocytes were isolated by Ficoll density gradient. Then the tissue lysates were filtered through 0.22 μm filter and 6 cases of these tissue lysates from each 2 groups were chosen randomly for the further migration assay. The other part of fresh tissue was formalin-fixed for the IHC staining.

2.2.3. Cell Culture

The BPH epithelial cell-line, BPH-1, was purchased from KeyGen Biotech Co., Ltd (KG1008, NJ, China) and the predominantly CD8(+) T-lymphocytic cell-line, Molt-3 [18], was purchased from the American Type Culture Collection (CRL-1552, Rockville, MD, USA) and grown in RPMI-1640 media containing 1% penicillin and streptomycin, supplemented with 10% fetal bovine serum (FBS). All cell lines were cultured in a 5% (v/v) CO₂ humidified incubator at 37°C. BPH-1 cells of charcoal medium group were treated with 10% charcoal treated fetal calf serum (SH30068.03, Hyclone, South Logan UT, USA) for 2 days, then collected supernatant and BPH-1 cells were harvested for the further experiment. Peripheral blood mononuclear cells (PBMC) that were isolated from human blood were grown in X-VIVO 15 medium (04-418Q, Lonza, NJ, USA) and all the further experiment would be finished in 2 days.

2.3. Methods

2.3.1. Immunohistochemistry

To determine the expression of CD4 and CD8 on the cell surface and intracellular CCL5 in BPH tissues, the specimens from TUR-P surgery were fixed in 4% buffered formalin overnight at 4°C and then dehydrated in an ascending ethanol series, routinely embedded in paraffin, and sectioned at 3 μm. After conventional deparaffinization, hydration, and antigen retrieve, endogenous peroxidase was inactivated by 3% hydrogen peroxide. The primary antibodies of the rabbit anti-CD4(+) (dilution 1 : 50, Abcam), anti-CD8(+) (dilution 1 : 50, Thermo), and the rabbit anti-CCL5 (+) (2 μg/mL, Abcam) were used for incubation at 4°C overnight. After washings with phosphate-buffered saline (PBS), the primary antibody was recognized by the biotinylated secondary antibody (PK-4001, Vector Labs, Burlingame, CA, USA) at room temperature for 30 min and visualized by VECTASTAIN ABC peroxidase system and peroxidase substrate DAB kit (SK-4100, Vector Labs).

The max density of CD4 positive or CD8 positive cell was defined as ratio between the maximum positive cell number and all of nuclear cell number under 100x field. And these indexes were average value by two operators who are blind to each other and were calculated with Image-Pro Plus 6.0 software (Media Cybernetics, Rockville, MD, USA).

Proteins expression of CCL5 was assessed semiquantitatively and a 4-tiered system (0 negative, 1 weak, 2 moderate, and 3 strong) was used. Two pathologists evaluated the stain strength and the final result was the average of their scores.

2.3.2. Flow Cytometry

To further study the T-cell subpopulation infiltration among the total T cell, the isolated lymphocytes from prostate tissues were analyzed by two-color flow cytometry for phenotypic characterization of T cells according to manufacturer’s procedure. Cells were resuspended in staining buffer (PBS containing 1% fetal bovine serum) and stained for 30 min at 4°C with anti-CD3 PE-Cy 7 and anti-CD4 FITC or anti-CD8 PE and their isotype control antibodies (both from BD Biosciences). Flow cytometry was done on a Becton Dickinson LSRII (BD Biosciences); cells were acquired and data were analyzed using Flow Jo software (BD Biosciences). Then the average percentage of CD4 positive or C8 positive among total T cell in each group was calculated. At the same time the CD8+ T cells from blood of healthy persons were also harvested by the same method.

2.3.3. Quantitative PCR

Total RNA was extracted from each cell line using Trizol (15596-018, Invitrogen, Grand Island, NY, USA). According to manufacturer’s protocol, cDNA was synthesized from 1 μg RNA, using a High capacity cDNA reverse transcription kit (4368813, Applied Biosystem, CA, USA). The standard PCR conditions included 2 minutes at 50°C and 10 min at 95°C followed by 40 cycles of extension at 95°C for 15 seconds and one minute at 60°C. Threshold lines were automatically adjusted to intersect amplification lines in the linear portion of the amplification curves and cycle to threshold (Ct) were recorded automatically. Data were normalized with GAPDH mRNA transcription (housekeeping gene) and the fold change in gene expression relative to normal was calculated using the ddCt method. The sequences of the gene primers are designed by Primer Premier 5 software (Premier Biosoft International, Palo Alto, CA, USA) and are shown in Table 1.

2.3.4. Migration Assay

To detect the recruitment of CD8+ T cell by tissue lysates and BPH-1 cells, the tissue lysates or of BPH-1 cells of different treatment were plated into the lower chamber of the transwells with 5 μM pore polycarbonate membrane inserts (3421 Corning, MA, USA). of CD8+ T cells isolated by flow cytometry from 6 healthy persons and Molt-3 cells were plated onto the upper chamber. After 6 hrs, the cells migrated into the lower chamber media were collected and counted by the Bio-Rad TC10 automatic cell counter. Each sample was assayed in triplicate and each case was repeated twice.

2.3.5. Statistical Analysis

Statistical analyses for continuous variables involved paired -test with SPSS 17.0 (SPSS Inc., Chicago, IL, USA). Data were also analyzed through one-way ANOVA coupled with the Newman-Keuls test and Mann-Whitney test. was considered statistically significant.

3. Results

3.1. The Influence of Finasteride Treatment on T Cell Population Infiltrating in BPH Prostate Tissue

We detected T-cell population infiltration between prostate tissue with/ without finasteride treatment [19]. Firstly, the immunohistochemical analysis using anti-CD4 and CD8 antibody showed that CD8+ T cells were identified surrounding the epithelium area, but CD4+ T cells in stromal area (Figures 1(a) and 1(b)).

(a)

(b)

(c)

Figure 1

The T-cell population infiltrating prostate tissue with/without finasteride treatment. (a) CD8 was stained from no medication group and finasteride group; scale bar: 100 μm and 20 μm. Negative controls were showed in the bottom left corner, respectively. Data presented as the percentage of CD8+ T-cell number in all of nuclear cell number (mean ± SEM); (-test). (b) Immunohistochemistry staining for CD4+ T infiltration. Magnification and negative control are the same as mentioned before. (c) Flow cytometry assay. Data presented as the rate of CD8+ or CD4+ T cells in total T cell (mean ± SEM). in the right column, (-test).

Furthermore, as shown in Figure 1(a), the max densities of CD8+ T cells infiltrated in the finasteride group and in the no medication group were , , and they were significantly higher in the finasteride group than in the no medication group (). However, CD4+ T cells infiltration showed no difference (Figure 1(b)). Then flow cytometry data was consistent with the IHC staining. The tissues of group 2 presented a significantly higher percentage of CD8 positive cells among all total T-lymphocytes than tissues of group 1 (21.36% versus 8.78%, Figure 1(c)).

3.2. The CD8+ T Cells Migration In Vitro

To study the potential cross talk between infiltrating CD8+ T cell and prostate epithelial cells as seen in BPH specimens (Figure 1), we established a coculture model for CD8+ T cell migration assay. As shown in Figures 2(a) and 2(b), more than 60% of CD8+ T from blood of health persons migrated to the prostate tissue lysates from the finasteride group. It was significantly higher than no medication group (64.02% versus 10.31%).

(a)

(b)

(c)

This data was then confirmed in BPH epithelial cell-line. As shown in Figure 2(c), BPH-1 cells which were pretreated with charcoal medium had more capability to recruit Molt-3 cells ().

3.3. Induction of Chemokines in BPH-1 Cells Stimulated by Changes of DHT Level

The q-PCR was used to assay for the most reported chemokines that are related to attracting T cells [20, 21] from BPH-1 cells with normal versus charcoal medium. The transcription of CCL5 mRNA in BPH-1 cells was higher in lower DHT condition () than those in normal condition () (Figure 3(a)). In addition, mRNA level of CCR5 was also upregulated nearly 3-fold in Molt-3 cells after coculture with BPH-1 cells in charcoal medium as shown in Figure 3(b).

(a)

(b)

(c)

Figure 3

Induction of chemokines in BPH-1 cells stimulated by changes of DHT level. (a) Q-PCR screening of a panel of cytokine factors that could be responsible for BPH-1 cell promoted T-cell migration. Compared to the BPH-1 cells cultured with normal medium, mRNA transcription of CCL5 was upregulated in BPH-1 cells with charcoal medium treatment; (-test). (b) Transcription of chemokine related receptors mRNA was detected by q-PCR. (ANOVA and Newman-Keuls test). (c) The interruption assay by adding CCL5 neutralizing antibody in above migration system. Data presented as the average cell numbers in lower chamber (mean ± SEM). (ANOVA and Newman-Keuls test).

Next, interruption assay was detected by using CCL5 neutralizing antibody in the migration system. It was shown that blocking CCL5 led to significantly suppressing the Molt-3 cells migration toward BPH-1 cells in low DHT condition Figure 3(c).

3.4. CCL5 Expression in Clinical Samples with/without Finasteride Treatment

The CCL5 expression was investigated in above BPH patients by IHC staining as shown in Figure 4. The results showed that CCL5 expression located in the epithelial area. Meanwhile, immunoreactive score was higher in the finasteride treatment group (2.79 ± 0.26), compared to the no medication group (1.41 ± 0.28).

(a)

(b)

4. Discussion

At present, so many studies have shown the role of chronic inflammation in BPH development. Cytokines, growth factors like IL6, IL8, IFN-r produced by T-lymphocytes, and BPH cells are involved in altering tissue remodeling and hyperplastic growth at each stage of BPH [2]. However, few literatures focused on the aetiology of BPH chronic inflammation. Potential causes include infectious agents, exposure to other environmental and dietary factors, and hormonal and metabolic derangements [22]. In this study, we aimed to dissect the induction of immune response by prostatic environmental factors.

It is reported that prostatic immune inflammatory cells consist of 70% T lymphocytes, 15% B-lymphocytes, and 15% macrophages, as well as mast cells [23] (and our unshown data). Hence, in the present study, we focused on the T-cell subpopulation. To the best of our knowledge, 6 months finasteride treatment means low intraprostatic DHT level in these patients [24]. The IHC and flow cytometry results showed that finasteride treatment could lead to more infiltration of CD8+ T cells but not CD4+ T cells.

The IHC results in this study showed CD8+ T cells localized surrounding epithelial area in BPH tissue. BPH epithelial is an important component of microenvironment in the prostate tissue. It can acquire the ability to express class II MHC molecules [25]. BPH epithelial cells have been previously described to act as a key cell, indicating their potential role in inducing and sustaining an autoimmune response within the prostatic gland [26]. To better investigate whether androgens could directly suppress T-cell infiltration, we performed migration assay by using BPH-1 cells and Molt-3 cells in vitro studies with/ without low androgen condition. Data in vitro were consistent with in vivo IHC staining.

Results in this study demonstrated that intraprostatic DHT has strong immune suppressive effects on CD8+ T cell infiltration induced by BPH epithelial cells. Some other groups have also discussed the similar study. Vignozzi et al. highlighted that DHT exerts an immune regulatory role on human prostatic stromal cells, inhibiting their potential to actively induce and/or sustain autoimmune and inflammatory responses [27]. Park and Shim found that finasteride might interfere with the anti-inflammatory reaction induced by doxazosin in combination of doxazosin and finasteride treatment [28]. Here we detected more patients and identified the T cell subsets which infiltrated in the prostatic tissue after finasteride treatment. Importantly, we also tried to find the key chemokine.

To further dissect how BPH-1 recruited more Molt-3 cells, we applied q-PCR to examine the expression of T cell related chemokines in BPH-1 cells at low DHT level. We found that CCL5 which functions as a chemokine playing a critical role in the recruitment of T cells [29] was expressed significantly higher in BPH-1 cells with androgen deprivation. We also found that CCR5 which is the natural CCL5 coreceptor [30] was upregulated in Molt-3 cells after coculture with BPH-1 cell in low androgen condition.

Then CCL5 expression was identified in the clinical sample mentioned above. Higher expression of CCL5 is showed in BPH tissues after finasteride treatment by immunohistochemistry. Importantly, the CCL5 was localized surrounding the epithelial area. In normal and BPH prostate tissue, infiltrating CD8+ T cells are mainly localized around epithelial ducts [31, 32]. Herein, the CCL5 expression was consistent with the distribution of CD8+ T cells. It suggested that CCL5 may be the key chemokine which secreted by BPH epithelial cells to recruit CD8+ T cells after anti-DHT therapy.

In conclusion, the most striking finding of the present study is that DHT exerts an immune regulatory role on human prostate epithelial cell, inhibiting their potential to actively induce inflammatory responses, and CCL5 which secreted by prostate epithelial cell is the key chemokine in this progression (Figure 5). Alternative anti-DHT therapy could lead to increased inflammation in prostatic tissue. This is might be a cause for treatment failure of 5α-reductase inhibitors. Anti-inflammation furthermore via targeting CCL5 combined with anti-DHT therapy in patients with BPH may be warranted in the future.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Yu Fan and Shuai Hu contributed equally to this work.

Acknowledgments

This work was supported by National Natural Science Foundation of China grants 81370858. The authors also thank Department of Urologic Pathology, Peking University First Hospital, for samples support.

References

J. T. Wei, E. Calhoun, and S. J. Jacobsen, “Urologic diseases in America project: benign prostatic hyperplasia,” Journal of Urology, vol. 173, no. 4, pp. 1256–1261, 2005.
View at: Publisher Site | Google Scholar
G. Gandaglia, A. Briganti, P. Gontero et al., “The role of chronic prostatic inflammation in the pathogenesis and progression of benign prostatic hyperplasia (BPH),” BJU International, vol. 112, no. 4, pp. 432–441, 2013.
View at: Google Scholar
C. K. M. Ho and F. K. Habib, “Estrogen and androgen signaling in the pathogenesis of BPH,” Nature Reviews Urology, vol. 8, no. 1, pp. 29–41, 2011.
View at: Publisher Site | Google Scholar
S. Aggarwal, S. Thareja, A. Verma, T. R. Bhardwaj, and M. Kumar, “An overview on 5α-reductase inhibitors,” Steroids, vol. 75, no. 2, pp. 109–153, 2010.
View at: Publisher Site | Google Scholar
J. D. McConnell, C. G. Roehrborn, O. M. Bautista et al., “The long-term effect of doxazosin, finasteride, and combination therapy on the clinical progression of benign prostatic hyperplasia,” The New England Journal of Medicine, vol. 349, no. 25, pp. 2387–2398, 2003.
View at: Publisher Site | Google Scholar
J. C. Nickel, C. G. Roehrborn, M. P. O'Leary, D. G. Bostwick, M. C. Somerville, and R. S. Rittmaster, “The relationship between prostate inflammation and lower urinary tract symptoms: examination of baseline data from the REDUCE trial,” European Urology, vol. 54, no. 6, pp. 1379–1384, 2008.
View at: Publisher Site | Google Scholar
G. Theyer, G. Kramer, I. Assmann et al., “Phenotypic characterization of infiltrating leukocytes in benign prostatic hyperplasia,” Laboratory Investigation, vol. 66, no. 1, pp. 96–107, 1992.
View at: Google Scholar
P. A. McArdle, K. Canna, D. C. McMillan, A.-H. McNicol, R. Campbell, and M. A. Underwood, “The relationship between T-lymphocyte subset infiltration and survival in patients with prostate cancer,” British Journal of Cancer, vol. 91, no. 3, pp. 541–543, 2004.
View at: Publisher Site | Google Scholar
I. G. Schauer and D. R. Rowley, “The functional role of reactive stroma in benign prostatic hyperplasia,” Differentiation, vol. 82, no. 4-5, pp. 200–210, 2011.
View at: Publisher Site | Google Scholar
Y. Bostanci, A. Kazzazi, S. Momtahen, J. Laze, and B. Djavan, “Correlation between benign prostatic hyperplasia and inflammation,” Current Opinion in Urology, vol. 23, no. 1, pp. 5–10, 2013.
View at: Google Scholar
B. Fibbi, G. Penna, A. Morelli, L. Adorini, and M. Maggi, “Chronic inflammation in the pathogenesis of benign prostatic hyperplasia,” International Journal of Andrology, vol. 33, no. 3, pp. 475–488, 2010.
View at: Publisher Site | Google Scholar
J. E. König, T. Senge, E. P. Allhoff, and W. König, “Analysis of the inflammatory network in benign prostate hyperplasia and prostate cancer,” Prostate, vol. 58, no. 2, pp. 121–129, 2004.
View at: Publisher Site | Google Scholar
W. Bushman, “Etiology, epidemiology, and natural history,” Urologic Clinics of North America, vol. 36, no. 4, pp. 403–415, 2009.
View at: Publisher Site | Google Scholar
L. Vignozzi, A. Morelli, E. Sarchielli et al., “Testosterone protects from metabolic syndrome-associated prostate inflammation: an experimental study in rabbit,” Journal of Endocrinology, vol. 212, no. 1, pp. 71–84, 2012.
View at: Publisher Site | Google Scholar
Z.-L. Wu, Y. Yuan, H. Geng, and S.-J. Xia, “Influence of immune inflammation on androgen receptor expression in benign prostatic hyperplasia tissue,” Asian Journal of Andrology, vol. 14, no. 2, pp. 316–319, 2012.
View at: Publisher Site | Google Scholar
C. K. Wong, P. T. Y. Wong, L. S. Tam, E. K. Li, D. P. Chen, and C. W. K. Lam, “Activation profile of Toll-like receptors of peripheral blood lymphocytes in patients with systemic lupus erythematosus,” Clinical and Experimental Immunology, vol. 159, no. 1, pp. 11–22, 2010.
View at: Publisher Site | Google Scholar
C. Guo, H. Liu, B.-H. Zhang, R. M. Cadaneanu, A. M. Mayle, and I. P. Garraway, “Epcam, cd44, and cd49f distinguish sphere-forming human prostate basal cells from a subpopulation with predominant tubule initiation capability,” PLoS ONE, vol. 7, no. 4, Article ID e34219, 2012.
View at: Publisher Site | Google Scholar
G. Harris, B. Azzolina, W. Baginsky et al., “Identification and selective inhibition of an isozyme of steroid 5α- reductase in human scalp,” Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 22, pp. 10787–10791, 1992.
View at: Publisher Site | Google Scholar
R. S. Rittmaster, “5α-reductase inhibitors in benign prostatic hyperplasia and prostate cancer risk reduction,” Best Practice and Research: Clinical Endocrinology and Metabolism, vol. 22, no. 2, pp. 389–402, 2008.
View at: Publisher Site | Google Scholar
A. E. Koch, “Chemokines and their receptors in rheumatoid arthritis: future targets?” Arthritis and Rheumatism, vol. 52, no. 3, pp. 710–721, 2005.
View at: Publisher Site | Google Scholar
K. A. Oldham, G. Parsonage, R. I. Bhatt et al., “T lymphocyte recruitment into renal cell carcinoma tissue: a role for chemokine receptors CXCR3, CXCR6, CCR5, and CCR6,” European Urology, vol. 61, no. 2, pp. 385–394, 2012.
View at: Publisher Site | Google Scholar
A. Briganti, U. Capitanio, N. Suardi et al., “Benign prostatic hyperplasia and its aetiologies,” European Urology, Supplements, vol. 8, no. 13, pp. 865–871, 2009.
View at: Publisher Site | Google Scholar
G. Kramer, G. E. Steiner, A. Handisurya et al., “Increased expression of lymphocyte-derived cytokines in benign hyperplastic prostate tissue, identification of the producing cell types, and effect of differentially expressed cytokines on stromal cell proliferation,” Prostate, vol. 52, no. 1, pp. 43–58, 2002.
View at: Publisher Site | Google Scholar
J. E. Edwards and R. A. Moore, “Finasteride in the treatment of clinical benign prostatic hyperplasia: a systematic review of randomised trials,” BMC Urology, vol. 2, p. 14, 2002.
View at: Google Scholar
G. Kramer, G. E. Steiner, P. Sokol, R. Mallone, G. Amann, and M. Marberger, “Loss of CD38 correlates with simultaneous up-regulation of human leukocyte antigen-DR in benign prostatic glands, but not in fetal or androgen-ablated glands, and is strongly related to gland atrophy,” BJU International, vol. 91, no. 4, pp. 409–416, 2003.
View at: Publisher Site | Google Scholar
G. Penna, B. Fibbi, S. Amuchastegui et al., “Human benign prostatic hyperplasia stromal cells as inducers and targets of chronic immuno-mediated inflammation,” Journal of Immunology, vol. 182, no. 7, pp. 4056–4064, 2009.
View at: Publisher Site | Google Scholar
L. Vignozzi, I. Cellai, R. Santi et al., “Antiinflammatory effect of androgen receptor activation in human benign prostatic hyperplasia cells,” Journal of Endocrinology, vol. 214, no. 1, pp. 31–43, 2012.
View at: Google Scholar
D. S. Park and J. Y. Shim, “Histologic influence of doxazosin and finasteride in benign prostatic hyperplasia accompanying chronic inflammation,” Urologia Internationalis, vol. 81, no. 4, pp. 441–446, 2008.
View at: Publisher Site | Google Scholar
C. M. Magro and X. Wang, “CCL5 expression in panniculitic T-cell dyscrasias and its potential role in adipocyte tropism,” The American Journal of Dermatopathology, vol. 35, no. 3, pp. 332–337, 2013.
View at: Google Scholar
J. Huber, F. W. Kiefer, M. Zeyda et al., “CC chemokine and CC chemokine receptor profiles in visceral and subcutaneous adipose tissue are altered in human obesity,” Journal of Clinical Endocrinology and Metabolism, vol. 93, no. 8, pp. 3215–3221, 2008.
View at: Publisher Site | Google Scholar
D. G. Bostwick, G. de la Roza, P. Dundore, F. A. Corica, and K. A. Iczkowski, “Intraepithelial and stromal lymphocytes in the normal human prostate,” Prostate, vol. 55, no. 3, pp. 187–193, 2003.
View at: Publisher Site | Google Scholar
G. E. Steiner, U. Stix, A. Handisurya et al., “Cytokine expression pattern in benign prostatic hyperplasia infiltrating T cells and impact of lymphocytic infiltration on cytokine mRNA profile in prostatic tissue,” Laboratory Investigation, vol. 83, no. 8, pp. 1131–1146, 2003.
View at: Publisher Site | Google Scholar

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Copyright © 2014 Yu Fan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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