Partial loss of contractile marker proteins in human testicular peritubular cells in infertility patients

Summary Fibrotic remodelling of the testicular tubular wall is common in human male infertility caused by impaired spermatogenesis. We hypothesized that this morphological change bears witness of an underlying fundamentally altered state of the cells building this wall, that is, peritubular smooth m...

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Veröffentlicht in:Andrology (Oxford) 2013-03, Vol.1 (2), p.318-324
Hauptverfasser: Welter, H., Kampfer, C., Lauf, S., Feil, R., Schwarzer, J. U., Köhn, F.‐M., Mayerhofer, A.
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container_issue 2
container_start_page 318
container_title Andrology (Oxford)
container_volume 1
creator Welter, H.
Kampfer, C.
Lauf, S.
Feil, R.
Schwarzer, J. U.
Köhn, F.‐M.
Mayerhofer, A.
description Summary Fibrotic remodelling of the testicular tubular wall is common in human male infertility caused by impaired spermatogenesis. We hypothesized that this morphological change bears witness of an underlying fundamentally altered state of the cells building this wall, that is, peritubular smooth muscle‐like cells. This could include a loss of the contractile abilities of these cells and thus be a factor in male infertility. Immune cells are increased in the tubular wall in these cases, hence local immune cell‐related factors, including a prostaglandin (PG) metabolite may be involved. To explore these points in the human, we used testicular biopsies, in which tubules with normal spermatogenesis and impaired spermatogenesis are next to each other [mixed atrophy (MA)], normal biopsies and cultured human testicular peritubular cells. Proteins essential for contraction, myosin heavy chain (MYH11), calponin (Cal) and relaxation, cGMP‐dependent protein kinase 1 (cGKI), were readily detected by immunohistochemistry and were equally distributed in all peritubular cells of biopsies with normal spermatogenesis. In all biopsies, vascular smooth muscle cells also stained and served as important intrinsic controls, which showed that in MA samples when spermatogenesis was impaired, staining was restricted to only few peritubular cells or was absent. When spermatogenesis was normal, regular peritubular staining became obvious. This pattern suggests complex regulatory influences, which in face of the identical systemic hormonal situation in MA patients, are likely caused by the local testicular micromilieu. The PG metabolite 15dPGJ2 may represent such a factor and it reduced Cal protein levels in peritubular cells from patients with/without impaired spermatogenesis. The documented phenotypic switch of peritubular, smooth muscle‐like cells in MA patients may impair the abilities of the afflicted seminiferous tubules to contract and relax and must now be considered as a part of the complex events in male infertility.
doi_str_mv 10.1111/j.2047-2927.2012.00030.x
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U. ; Köhn, F.‐M. ; Mayerhofer, A.</creator><creatorcontrib>Welter, H. ; Kampfer, C. ; Lauf, S. ; Feil, R. ; Schwarzer, J. U. ; Köhn, F.‐M. ; Mayerhofer, A.</creatorcontrib><description>Summary Fibrotic remodelling of the testicular tubular wall is common in human male infertility caused by impaired spermatogenesis. We hypothesized that this morphological change bears witness of an underlying fundamentally altered state of the cells building this wall, that is, peritubular smooth muscle‐like cells. This could include a loss of the contractile abilities of these cells and thus be a factor in male infertility. Immune cells are increased in the tubular wall in these cases, hence local immune cell‐related factors, including a prostaglandin (PG) metabolite may be involved. To explore these points in the human, we used testicular biopsies, in which tubules with normal spermatogenesis and impaired spermatogenesis are next to each other [mixed atrophy (MA)], normal biopsies and cultured human testicular peritubular cells. Proteins essential for contraction, myosin heavy chain (MYH11), calponin (Cal) and relaxation, cGMP‐dependent protein kinase 1 (cGKI), were readily detected by immunohistochemistry and were equally distributed in all peritubular cells of biopsies with normal spermatogenesis. In all biopsies, vascular smooth muscle cells also stained and served as important intrinsic controls, which showed that in MA samples when spermatogenesis was impaired, staining was restricted to only few peritubular cells or was absent. When spermatogenesis was normal, regular peritubular staining became obvious. This pattern suggests complex regulatory influences, which in face of the identical systemic hormonal situation in MA patients, are likely caused by the local testicular micromilieu. The PG metabolite 15dPGJ2 may represent such a factor and it reduced Cal protein levels in peritubular cells from patients with/without impaired spermatogenesis. The documented phenotypic switch of peritubular, smooth muscle‐like cells in MA patients may impair the abilities of the afflicted seminiferous tubules to contract and relax and must now be considered as a part of the complex events in male infertility.</description><identifier>ISSN: 2047-2919</identifier><identifier>EISSN: 2047-2927</identifier><identifier>DOI: 10.1111/j.2047-2927.2012.00030.x</identifier><identifier>PMID: 23413143</identifier><language>eng</language><publisher>Schaumburg, IL: American Society of Andrology</publisher><subject>Biological and medical sciences ; Biomarkers ; Biopsy ; Birth control ; Calcium-Binding Proteins - genetics ; Calcium-Binding Proteins - metabolism ; Calponins ; Contractile Proteins - genetics ; Contractile Proteins - metabolism ; contractility ; Cyclic AMP-Dependent Protein Kinases - genetics ; Cyclic AMP-Dependent Protein Kinases - metabolism ; differentiation ; Fundamental and applied biological sciences. Psychology ; Gynecology. Andrology. Obstetrics ; Humans ; immune cells ; Infertility, Male - genetics ; Infertility, Male - metabolism ; Kinases ; Male ; Male genital diseases ; male infertility ; Mammalian male genital system ; Medical sciences ; Microfilament Proteins - genetics ; Microfilament Proteins - metabolism ; Muscle, Smooth, Vascular ; Myosin Heavy Chains - genetics ; Myosin Heavy Chains - metabolism ; Prostaglandin D2 - analogs &amp; derivatives ; prostaglandins ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Seminiferous Tubules - metabolism ; Seminiferous Tubules - pathology ; Smooth muscle ; smooth muscle cells ; Sperm Motility ; Spermatogenesis ; Spermatogenesis - genetics ; Sterility. 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U.</creatorcontrib><creatorcontrib>Köhn, F.‐M.</creatorcontrib><creatorcontrib>Mayerhofer, A.</creatorcontrib><title>Partial loss of contractile marker proteins in human testicular peritubular cells in infertility patients</title><title>Andrology (Oxford)</title><addtitle>Andrology</addtitle><description>Summary Fibrotic remodelling of the testicular tubular wall is common in human male infertility caused by impaired spermatogenesis. We hypothesized that this morphological change bears witness of an underlying fundamentally altered state of the cells building this wall, that is, peritubular smooth muscle‐like cells. This could include a loss of the contractile abilities of these cells and thus be a factor in male infertility. Immune cells are increased in the tubular wall in these cases, hence local immune cell‐related factors, including a prostaglandin (PG) metabolite may be involved. To explore these points in the human, we used testicular biopsies, in which tubules with normal spermatogenesis and impaired spermatogenesis are next to each other [mixed atrophy (MA)], normal biopsies and cultured human testicular peritubular cells. Proteins essential for contraction, myosin heavy chain (MYH11), calponin (Cal) and relaxation, cGMP‐dependent protein kinase 1 (cGKI), were readily detected by immunohistochemistry and were equally distributed in all peritubular cells of biopsies with normal spermatogenesis. In all biopsies, vascular smooth muscle cells also stained and served as important intrinsic controls, which showed that in MA samples when spermatogenesis was impaired, staining was restricted to only few peritubular cells or was absent. When spermatogenesis was normal, regular peritubular staining became obvious. This pattern suggests complex regulatory influences, which in face of the identical systemic hormonal situation in MA patients, are likely caused by the local testicular micromilieu. The PG metabolite 15dPGJ2 may represent such a factor and it reduced Cal protein levels in peritubular cells from patients with/without impaired spermatogenesis. The documented phenotypic switch of peritubular, smooth muscle‐like cells in MA patients may impair the abilities of the afflicted seminiferous tubules to contract and relax and must now be considered as a part of the complex events in male infertility.</description><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Biopsy</subject><subject>Birth control</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Calponins</subject><subject>Contractile Proteins - genetics</subject><subject>Contractile Proteins - metabolism</subject><subject>contractility</subject><subject>Cyclic AMP-Dependent Protein Kinases - genetics</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>differentiation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>immune cells</subject><subject>Infertility, Male - genetics</subject><subject>Infertility, Male - metabolism</subject><subject>Kinases</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>male infertility</subject><subject>Mammalian male genital system</subject><subject>Medical sciences</subject><subject>Microfilament Proteins - genetics</subject><subject>Microfilament Proteins - metabolism</subject><subject>Muscle, Smooth, Vascular</subject><subject>Myosin Heavy Chains - genetics</subject><subject>Myosin Heavy Chains - metabolism</subject><subject>Prostaglandin D2 - analogs &amp; derivatives</subject><subject>prostaglandins</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Seminiferous Tubules - metabolism</subject><subject>Seminiferous Tubules - pathology</subject><subject>Smooth muscle</subject><subject>smooth muscle cells</subject><subject>Sperm Motility</subject><subject>Spermatogenesis</subject><subject>Spermatogenesis - genetics</subject><subject>Sterility. Assisted procreation</subject><subject>testis</subject><subject>Testis - metabolism</subject><subject>Testis - pathology</subject><subject>Vertebrates: reproduction</subject><issn>2047-2919</issn><issn>2047-2927</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkdtqGzEQhkVJaELiVyiCUMiNXR32CL0JSXMA04TSXgtZO6JyZK0jaUn89p21XRdyVSGYgflm9OsfQihnM47ny3ImWFFPRStqzLiYMcYkm719IKeHwtEh5-0JmaS0RIg14xUfyYmQBZe8kKfEPemYnfbU9ynR3lLThxy1yc4DXen4DJGuY5_BhURdoL-HlQ40Q8rODF5jEaLLw2KbG_B-S7lgAcd6lzd0rbODkNM5ObbaJ5js4xn5dfvt5_X9dP5493B9NZ-aohVsWhtRMq1l27FOQ2NLKW1lMVqAzkJRybo1RSkWRlam7KS2kkkrwLTSlmXJ5Bm53M1F2S8DClUrl0ZlOkA_JMVF0-Df60IievEOXfZDDKhO8Uo2ghcVr5FqdpSJ6FEEq9bRoTUbxZkaN6KWajRbjcarcSNquxH1hq2f9g8MixV0h8a__iPweQ_oZLS3UQfj0j-uZqigHbmvO-4V97L5bwHq6vvND_TnDyHLp4k</recordid><startdate>201303</startdate><enddate>201303</enddate><creator>Welter, H.</creator><creator>Kampfer, C.</creator><creator>Lauf, S.</creator><creator>Feil, R.</creator><creator>Schwarzer, J. 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Immune cells are increased in the tubular wall in these cases, hence local immune cell‐related factors, including a prostaglandin (PG) metabolite may be involved. To explore these points in the human, we used testicular biopsies, in which tubules with normal spermatogenesis and impaired spermatogenesis are next to each other [mixed atrophy (MA)], normal biopsies and cultured human testicular peritubular cells. Proteins essential for contraction, myosin heavy chain (MYH11), calponin (Cal) and relaxation, cGMP‐dependent protein kinase 1 (cGKI), were readily detected by immunohistochemistry and were equally distributed in all peritubular cells of biopsies with normal spermatogenesis. In all biopsies, vascular smooth muscle cells also stained and served as important intrinsic controls, which showed that in MA samples when spermatogenesis was impaired, staining was restricted to only few peritubular cells or was absent. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Wiley Online Library Free Content
subjects Biological and medical sciences
Biomarkers
Biopsy
Birth control
Calcium-Binding Proteins - genetics
Calcium-Binding Proteins - metabolism
Calponins
Contractile Proteins - genetics
Contractile Proteins - metabolism
contractility
Cyclic AMP-Dependent Protein Kinases - genetics
Cyclic AMP-Dependent Protein Kinases - metabolism
differentiation
Fundamental and applied biological sciences. Psychology
Gynecology. Andrology. Obstetrics
Humans
immune cells
Infertility, Male - genetics
Infertility, Male - metabolism
Kinases
Male
Male genital diseases
male infertility
Mammalian male genital system
Medical sciences
Microfilament Proteins - genetics
Microfilament Proteins - metabolism
Muscle, Smooth, Vascular
Myosin Heavy Chains - genetics
Myosin Heavy Chains - metabolism
Prostaglandin D2 - analogs & derivatives
prostaglandins
RNA, Messenger - genetics
RNA, Messenger - metabolism
Seminiferous Tubules - metabolism
Seminiferous Tubules - pathology
Smooth muscle
smooth muscle cells
Sperm Motility
Spermatogenesis
Spermatogenesis - genetics
Sterility. Assisted procreation
testis
Testis - metabolism
Testis - pathology
Vertebrates: reproduction
title Partial loss of contractile marker proteins in human testicular peritubular cells in infertility patients
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