Literature DB >> 15711366

The healthy rat prostate contains high levels of natural killer-like cells and unique subsets of CD4+ helper-inducer T cells: implications for prostatitis.

Eugene V Vykhovanets1, Martin I Resnick, Susan Ruth Marengo.   

Abstract

PURPOSE: Chronic nonbacterial prostatitis spontaneously develops in aged Lewis and Wistar rats but not in Sprague-Dawley rats. We report the unique profile of lymphocyte subsets present in the healthy Sprague-Dawley rat prostate.
MATERIALS AND METHODS: We compared enzymatic and mechanical methods of intraprostatic lymphocyte isolation in healthy 8 to 10-week-old Sprague-Dawley rats. Mechanical isolation was chosen because of its superior preservation of surface antigens. Intraprostatic lymphocyte subsets were analyzed by flow cytometry.
RESULTS: Levels of prostatic alphabetaTCR+ T cells were similar and levels of prostatic B cells were decreased 5 to 10-fold compared with those found in other tissues (p </=0.005). Unexpectedly two-thirds of the total prostatic lymphocytes expressed the natural killer (NK) marker CD161a+. They were divided equally between NK (CD161a+alphabetaTCR) and NKT (CD161a+alphabetaTCR+) cells. Of prostatic CD161a+ cells 50% to 60% were also CD8+. Levels of NKT cells were dramatically lower in other tissues (p </=0.005) and they never accounted for more than 8% of total lymphocytes. The prostate contained lower levels of CD4+ T cells than all tissues except the liver (p </=0.005) and higher levels of CD8+ T cells than any other tissue studied (p </=0.05), resulting in an inverted CD4-to-CD8 ratio. CD45RC+CD4+alphabetaTCR+ T cells and CD161a+CD4+alphabetaTCR+ NKT cells were elevated in the prostate (p </=0.02).
CONCLUSIONS: The healthy rat prostate contains an unusually high proportion of NK and NKT cells. The balance between the CD45RC+CD4+alphabetaTCR+ T cells, which initiate the cell mediated immune response, and CD4+ NKT cells, which can suppress autoimmunity, may be a key in understanding the resistance of Sprague-Dawley rats to chronic nonbacterial prostatitis.

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Year:  2005        PMID: 15711366     DOI: 10.1097/01.ju.0000149130.06055.f2

Source DB:  PubMed          Journal:  J Urol        ISSN: 0022-5347            Impact factor:   7.450


  5 in total

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Authors:  Shaun Wen Huey Lee; Men Long Liong; Kah Hay Yuen; John N Krieger
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Review 2.  Inflammation and benign prostatic hyperplasia.

Authors:  J Curtis Nickel
Journal:  Urol Clin North Am       Date:  2008-02       Impact factor: 2.241

Review 3.  Inflammatory mediators in the development and progression of benign prostatic hyperplasia.

Authors:  Cosimo De Nunzio; Fabrizio Presicce; Andrea Tubaro
Journal:  Nat Rev Urol       Date:  2016-09-30       Impact factor: 14.432

4.  Combined treatment with dihydrotestosterone and lipopolysaccharide modulates prostate homeostasis by upregulating TNF-α from M1 macrophages and promotes proliferation of prostate stromal cells.

Authors:  Yu Tong; Yi-Jun Guo; Qin Zhang; Hai-Xia Bi; Kai Kai; Ren-Yuan Zhou
Journal:  Asian J Androl       Date:  2022 Sep-Oct       Impact factor: 3.054

5.  Etiopathogenesis of benign prostatic hypeprlasia.

Authors:  Jie Tang; Jingchun Yang
Journal:  Indian J Urol       Date:  2009-07
  5 in total

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