Table of Contents  
ORIGINAL ARTICLE
Year : 2019  |  Volume : 21  |  Issue : 6  |  Page : 570-576

Autophagy is increased in cryptorchid testis resulting in abnormal spermatozoa


1 Univ Rennes, CHU Rennes, Laboratoire de Biologie de la Reproduction -CECOS, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085, Rennes F-35000, France
2 Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, 194223 St-Petersburg, Russia
3 Univ Rennes, Biosit Platform - MRIC, Rennes 35000, France
4 Univ Rennes, CHU Rennes, Department of Gynecology Obstetric and Human Reproduction, Rennes 35000, France
5 Univ Rennes, CHU Rennes, Department of Cytogenetic, Irset (Institute for Environmental and Occupational Health) – UMR_S 1085, Rennes 35000, France
6 Univ Rennes, Inserm, EHESP, Irset (Institute for Environmental and Occupational Health) – UMR_S 1085, Rennes F-35000, France
7 University of Poitiers - CHU Poitiers, STIM ERL 7003 CNRS, Poitiers 86021, France

Date of Submission28-May-2018
Date of Acceptance10-Jan-2019
Date of Web Publication24-Apr-2019

Correspondence Address:
Celia Ravel
Univ Rennes, CHU Rennes, Laboratoire de Biologie de la Reproduction -CECOS, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail) - UMR_S 1085,Rennes F-35000
France
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/aja.aja_12_19

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  Abstract 


Autophagy is involved in spermatogenesis by regulating germ cell maturation. This catabolic process increases with hyperthermic conditions to prevent the accumulation of damaged organelles. Cryptorchidism is associated with impairment of germ cell maturation revealed by the presence of immature forms of sperm cells in ejaculates. The aim of the present study was to evaluate the status of autophagy in sperm cells from cryptorchid patients. Semen samples of cryptorchid patients and normozoospermic controls were analyzed by immunocytochemistry and electron microscopy. Autophagy proteins, autophagy-related protein 9 (ATG9) and microtubule-associated protein, 1A/1B-light chain 3 (LC3) were localized by immunocytochemistry on the acrosome and on the equatorial segment of sperm cells. LC3 was also detected in the midpiece of cryptorchid sperm tail. Autophagy substrate p62 protein was present in the acrosome and in the postequatorial segment of sperm in control samples, but not in the cryptorchid ones. Transmission electron microscopy revealed double-membrane-limited autophagosomes in postequatorial part of spermatozoa head and midpiece in cryptorchid samples. Partly degraded mitochondria were frequently discerned in autophagic vacuoles. In conclusion, autophagy is increased in sperm cells from patients with cryptorchid history comparatively to control. Our work provides insights into the role of autophagy in the maturation and survival of human male gametes in pathological conditions. Thus, regulating autophagy could represent a potential way to improve sperm quality in cryptorchid men.

Keywords: autophagy; cryptorchidism; mitophagy; spermatozoa


How to cite this article:
Yefimova MG, Buschiazzo A, Burel A, Lavault MT, Pimentel C, Jouve G, Jaillard S, Jegou B, Bourmeyster N, Ravel C. Autophagy is increased in cryptorchid testis resulting in abnormal spermatozoa. Asian J Androl 2019;21:570-6

How to cite this URL:
Yefimova MG, Buschiazzo A, Burel A, Lavault MT, Pimentel C, Jouve G, Jaillard S, Jegou B, Bourmeyster N, Ravel C. Autophagy is increased in cryptorchid testis resulting in abnormal spermatozoa. Asian J Androl [serial online] 2019 [cited 2019 Dec 16];21:570-6. Available from: http://www.ajandrology.com/text.asp?2019/21/6/570/257243 - DOI: 10.4103/aja.aja_12_19




  Introduction Top


Cryptorchidism or maldescended testes is the most common developmental abnormality, with the incidence of 2%–8% in full-term boys and 30%–33% in premature boys.[1] Factors influencing testicular descend are grouped as genetic, hormonal and environmental, or their combination.[2] Cryptorchidism is associated with impaired spermatogenesis.[3],[4] Abnormal intra-abdominal environment of cryptorchid testes and exposition to elevated temperature strongly affect both germ and somatic cells, which display dramatic changes in morphology, function, and gene expression.[5] Aberrant structure of Leydig cells,[6],[7] vacuolization of Sertoli cell, abnormal cell adhesion and disruption of Sertoli-cell supported blood-testis barrier are the consequences of cryptorchidism in human[6],[8],[9] and animal experimental models.[7],[10],[11] Besides, epididymal anomalies are often associated with the undescended testis.[12],[13]

Cryptorchidism is recognized as one of the strongest risk factors for infertility in adulthood,[14],[15],[16] as confirmed by experimental and epidemiologic studies.[5] While the surgical correction of cryptorchidism (orchidopexy) in children is considered as an efficient mode of treatment, both structural and functional alterations are detected in the testes with a history of cryptorchidism.[14] The decrease of semen quality (sperm cell number, motility, and sperm cell malformations), and the presence of immature forms of spermatozoa with uncondensed nuclei, aberrant acrosomes, and large cytoplasmic residues have been reported in men who underwent orchidopexy for cryptorchidism during childhood.[15],[16],[17] Serum hormones level also deviates from normal values so an increase of follicle-stimulating and luteinizing hormones or a decrease of inhibin was, for example, detected in men subjected to orchidopexy in the childhood.[18]

Autophagy is a catabolic pathway which takes place in all eukaryotic cells. It provides the transport of nonessential, old or damaged components to lysosomes for lysosome-mediated degradation and turnover process.[19] Autophagic degradation of damaged mitochondria (mitophagy) is a sort of selective autophagy. It plays critical roles in fundamental biological processes such as terminal differentiation of red blood cells and paternal mitochondrial degradation, as well as in pathological states, including some neurodegenerative diseases, ischemia or drug-induced tissue injury.[20] In contrast to apoptosis, which is a programmed cell death,[21] autophagy is primarily a cell survival process, which intervenes under various conditions of cellular stress, such as starvation, hyperthermia, and different cytotoxic insults, thereby conferring adaptation to the changing environment.[19],[20] Nevertheless, uncontrolled activation of autophagy can promote cell death, of which morphological appearance differs from those of apoptosis.[19],[21]

Autophagy is regulated by the autophagy-related (ATG) genes originally identified in yeast and their mammalian homologs.[19] Being initiated, autophagy progresses through a series of consecutive steps, starting from the formation of a pre-autophagosomal membrane phagophore, its further maturation into a double-membrane-limited autophagosome, which then fuses with lysosome for degradation of sequestered cargoes. Several proteins can be used as specific markers to evaluate the progression of autophagy such as ATG9 protein at the phagophore assembly, microtubule-associated protein, 1A/1B-light chain 3 (LC3)-II protein (membrane form of LC3 protein) at the stage of elongation and formation of autophagosome or p62 protein (which is a selective autophagy substrate protein) at the final stage of autophagy.[19] Nevertheless, high-resolution transmission electron microscopy allowing to distinguish double-membrane-limited vacuoles filled with different cargoes remains the “gold standard” to assess autophagy in tissues.[22]

Autophagy has been shown to regulate germ cell maturation in animal models.[23],[24] It interferes at the spermiation stage when round spermatids undergo metamorphosis process leading to the formation of the streamlined spermatozoa.[25] Conditional knockout of autophagy-related genes in mice severely affects the fertility, resulting in generation of functionally disabled spermatozoa showing the signs of immaturity (malformed and/or absent acrosome, large cytoplasmic droplet, and decreased motility[23],[24]), resembling those observed in cryptorchid animals.[26],[27],[28]

Autophagy is known to be initiated in hyperthermic conditions under which it acts as the primary cytoprotective mechanism, preventing the accumulation of protein aggregates and damaging organelles formed in cells exposed to heat shock.[29] Elevated environmental temperature within the body cavity is believed to be a primary factor affecting spermatogenesis in cryptorchid testes.[30],[31],[32] While the molecular mechanisms behind this have not been fully determined, later stage haploid germ cells seem to be the most susceptible when exposed to abdominal temperature.[5] A study from experimental cryptorchid rat model revealed an involvement of autophagy in testicular spermatogenesis damage.[33]

To our knowledge, no information on autophagy status in sperm cells from patients with cryptorchid history is available to date. In this work, we aimed to evaluate the status of autophagy in spermatozoa from patients who underwent orchidopexy during childhood by immunohistochemistry and electron microscopy.


  Patients and Methods Top


Patients

Semen samples were obtained from the French Biobank GERMETHEQUE from 10 patients with cryptorchid history and 8 as control individuals attending the Laboratory of Reproductive Biology CECOS (University Hospital Center of Rennes, Rennes, France) for assisted reproduction technology or before vasectomy, respectively. All patients displayed a normal karyotype and neither radiotherapy history nor chemotherapy. The study was approved by the Local Ethics Committee (CE GMR 17-03 Rennes, France) and was conducted in accordance with the Helsinki II declaration and with the French law on clinical research. Informed and written consent was obtained from all individual participants included in the study.

Semen collection

Semen samples of the patients were collected by masturbation after 3–5 days of sexual abstinence and examined after liquefaction for 30 min at 37°C. Sperm volume and pH, concentration and motility of spermatozoa were evaluated according to the World Health Organization guidelines.[34]

Immunocytochemistry

Semen samples were smeared on Thermo Scientific™ SuperFrost™microscope glass slides (Z692255-100EA, Sigma-Aldrich, St. Louis, MO, USA). Samples were then fixed with 4% paraformaldehyde (PFA)/PBS (R37814, Invitrogen, Waltham, MA, USA; BE17-512F, Lonza, Basel, Switzerland) for 10 min, washed three times with PBS and dried out at room temperature for 1 h. The samples were permeabilized with 0.1% Triton X-100/PBS (T8787, Sigma-Aldrich), briefly washed and incubated overnight with primary antibodies diluted 1:250 in 1% bull serum albumin (BSA)/PBS (A9647, Sigma-Aldrich) at 4°C. All primary antibodies were rabbit polyclonal antibodies from Novus biologicals (anti ATG9 (NB110-56893), anti LC3 (NB100-2220) and anti p62 (NBP1-48320); Centennial, CO, USA). Next day the samples were washed in PBS, and then incubated with secondary antibodies (Chicken anti-Rabbit Alexa-448, dilution 1:500 in 1% BSA/PBS; A-21441, Invitrogen), at room temperature for 1 h, washed and counterstained with 0.5 μg ml−1 4,6-diaminido-2-phenylindole (DAPI, 62247, Thermo Fisher Scientific, Waltham, MA, USA). To check for the specificity of antibodies, the control experiments were carried out using the control peptides from Novus biologicals: NB110-56893PEP (for ATG9) and NB100-2220PEP (for LC3) according to the supplier's protocol. To this end, 5 μl (10 × excess) of blocking peptide was added to 250 μl of the primary antibody (dilution 1:250 in 1% BSA/PBS). The mix was incubated for 1 h at room temperature with gentle stirring, and then dropped on the slides. The slides were incubated overnight at 4°C and then processed as described above. In additional control experiments, a nonimmune rabbit serum (933B-02, MERCK, Darmstadt, Germany; dilution 1:250 in 1% BSA/PBS) was applied instead of the primary antibody. The slides were observed under an upright Nikon Eclipse NiE microscope (Nikon Instruments Europe B.V., Amstelveen, the Netherlands). The pictures were taken using an Orca–R2 C10600 camera (Hamamatsu, Hamamatsu City, Japan).

Transmission electron microscopy (TEM)

Semen samples were diluted in Ferticult IVF medium (FECV050, Fertipro, Beernem, Belgium) 1:5 (v/v), then centrifuged at 600g for 10 min (Heraeus Multifuge X1R Centrifuge 75004250, Thermo Fisher Scientific, Osterode am Harz, Germany). The pellet was fixed in 2.5% glutaraldehyde (16220, Electron Microscopy Sciences, Hatfield, PA, USA)/cacodylate buffer (0.1 mol l−1, pH 7.2; 11650, Electron Microscopy Sciences), at room temperature for 1 h, then washed in cacodylate buffer for a further 30 min. The samples were postfixed in 1% osmium tetroxide (19150, Electron Microscopy Science) for 1 h at room temperature, then dehydrated through graded alcohol series (20821.296, VWR Chemicals, Radnor, PA, USA), and embedded in Epon 812 resin (45345, Sigma-Aldrich). Ultrathin sections of 80 nm were cut using Leica Ultracut UCT Ultramicrotome (Leica Biosystems, Wetzlar, Germany), contrasted with uranyl acetate and examined at 120 kV with a JSM-4000 electron microscope (JEOL, Tokyo, Japan). Images were captured digitally by an Orius 1000 camera (Gatan, Abingdon, United Kingdom).

Statistical analyses

GraphPad Prism Software (GraphPad Software, Inc., San Diego, CA, USA) was used to conduct statistical analyses. Two-tailed Student's t-test for unpaired data was used to evaluate single comparisons between different experimental groups, which exhibited Gaussian distribution as checked by Shapiro–Wilk normality test using GraphPad Prism Software. Differences were considered statistically significant for a value of P < 0.05.


  Results Top


Clinical data

Ten cryptorchid patients attending the Laboratory of Reproductive Biology CECOS (University Hospital Center of Rennes, France) for assisted reproduction technology and eight normozoospermic individuals before vasectomy were enrolled in this study. The results from clinical analysis are summarized in [Table 1]. The data show a strong decrease of semen parameters (concentration, mobility, and the percentage of normal forms of spermatozoa) in men with cryptorchid history.
Table 1: Semen parameter values (mean±standard error) of men with cryptorchid history and fertile control

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Immunolocalization of autophagy-related proteins in spermatozoa from cryptorchid and control patients

To assess the autophagy status in cryptorchid spermatozoa, we analyzed the immunodistribution of autophagy proteins which are specific markers of different stages of autophagy in comparison with the control samples.

In both normal and cryptorchid spermatozoa, the early autophagy marker ATG9 protein was mainly detected in the sperm head, namely, in its apical region [Figure 1]. Isolated anti-ATG9 points were also detected in the spermatozoon neck, probably in association with the basal body [Figure 1]a, inset 1, arrowhead). In some spermatozoa from both normal and cryptorchid patients, a very strong anti-ATG9 immunoreactivity was noticed in the sperm head equatorial segment, whereas the apical region was almost free of anti-ATG9 immunostaining [Figure 1]a, inset 2; [Figure 1]b, inset 2). In control preparations (treatment of samples with primary antibody preincubated with ATG9 blocking peptide), only a faint homogenous green staining was observed in both spermatozoon head and tail [Figure 1]c. We divided the ATG9 staining profiles in the specimens from control and cryptorchid patients into two types (type 1 and type 2; [Figure 1] legend). Statistical analysis did not reveal significant difference in the repartition of ATG9 staining profiles between both groups analyzed [Figure 1]d.
Figure 1: Immunodistribution of ATG9 protein in spermatozoa from (a) normal and (b) cryptorchid patients. IF analysis shows anti-ATG9 staining (green) in apical region of sperm head (type 1 staining), spermatozoon neck (arrowhead) and sperm head equatorial segment (type 2 staining, arrow). The pictures were merged with DAPI-stained nuclei (blue). 1 and 2 are higher magnifications of fragments from a and b. (c) A control specimen treated with the primary antibody preincubated with corresponding blocking peptide (see Patients and Methods; upper panel). Bottom panel is the merge with DAPI-stained nuclei. All pictures in a, b, and c were taken at the same exposition time. (d) Histogram showing the relative quantity of type 1 and type 2 spermatozoa in the preparations from normal and cryptorchid patients. ATG9: autophagy-related 9; IF: immunofluorescence; DAPI: 4,6-diaminido-2-phenylindole.

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The immunolocalization of the autophagosome marker LC3 protein was not the same as that of ATG9. In control spermatozoa, the anti-LC3 immunostaining was detected in the acrosome and in the midpiece of the tail [Figure 2]a. In some cases, faint immunostaining was also detected in the flagellum [Figure 2]a. Some spermatozoa from normozoospermic patients also exhibited a strong anti-LC3 immunoreactivity in the sperm head equatorial segment ([Figure 2]a, arrow). In spermatozoa from men with cryptorchid history, anti-LC3 immunoreactivity was more pronounced compared to the control. The strongest anti-LC3 immunoreactivity was detected in the spermatozoon tail. Indeed, the neck and the midpiece were strongly stained with anti-LC3 antibodies [Figure 2]b. Of note is that both the axial filament and the end piece of the flagellum were also stained with anti-LC3 antibodies. We divided LC3 staining profiles in the specimens from control and cryptorchid spermatozoa into two types (type 1 and type 2; [Figure 2] legend). In type 1 spermatozoa, a faint anti-LC3 immunostaining was detected in spermatozoa head and tail, including axial filament, whereas in type 2 spermatozoa, anti-LC3 immunostaining was present in the equatorial segment, in the acrosome and in the midpiece of the tail. Control experiments using LC-3 blocking peptide demonstrated the specificity of LC-3 staining [Figure 2]c. Statistical analysis revealed the quasi-equivalence of type 1 and type 2 LC3-immunodistribution in cryptorchid patients compared to the control, in which the type 2 immunodistribution was prevalent [Figure 2]d.
Figure 2: Immunodistribution of LC3 and p62 proteins in spermatozoa from normal and cryptorchid patients. (a) Faint anti-LC3 immunoreactivity (green) is detected in spermatozoa head and tail including axial filament (type 1 staining); in head equatorial segment (arrow), acrosome and the midpiece of the tail (type 2 staining). Note no staining in the axial filament and the end piece of flagellum in type 2 spermatozoa (arrowhead). (b) Pronounced anti-LC3 immunostaining is detected in acrosome and along the tail of cryptorchid spermatozoa including axial filament and end piece of flagellum (type 1 staining); very strong anti-LC3 immunostaining is present in the midpiece (b, arrowhead), but not in the axial filament in type 2 spermatozoa. (c) A control specimen treated with the primary antibody preincubated with LC3-blocking peptide (see Patients and Methods; upper panel). Bottom panel is the merge with DAPI-stained nuclei. (d) Histogram showing the relative quantity of type 1 and type 2 spermatozoa in the preparations from normal and cryptorchid patients. (e) Postacrosomal region (arrow) of control spermatozoa and the midpiece of the tail were stained with anti-p62 antibodies. (f) Anti-p62 immunostaining in cryptorchid spermatozoa. (g) Control specimen incubated with nonimmune rabbit serum instead of the primary antibody (upper panel). Bottom panel is the merge with DAPI-stained nuclei. (h) Histogram showing the relative quantity of spermatozoa stained with anti-p62 antibodies in the preparations from normal and cryptorchid patients.**P<0.05. LC3: microtubule-associated protein, 1A/1B-light chain 3; DAPI: 4,6- diaminido-2-phenylindole.

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In control specimens, immunostaining against autophagy substrate p62 protein was detected in the postacrosomal region of the spermatozoa and in the midpiece of the tail [Figure 2]e. No specific anti-p62 immunostaining was detected in sperm cells from the patients with cryptorchid history [Figure 2]f. Control experiments using rabbit non-immune serum demonstrated the specificity of p62 staining [Figure 2]g. Only rare spermatozoa from cryptorchid patients presented a faint anti-p62 immunostaining [Figure 2]f and [Figure 2]h.

Thus, the distribution of several autophagy-related proteins in cryptorchid spermatozoa shows a deviation compared to the control. To confirm our immunocytochemistry results, we carried out a TEM analysis to compare spermatozoa from control and from patients.

TEM analysis of spermatozoa from cryptorchid and control patients

TEM analysis revealed numerous morphological abnormalities in sperm samples from cryptorchid patients. Immature forms of spermatozoa were extremely frequent in those specimens. Immature cells were recognized by misshapen, round or elliptic nuclei with uncondensed chromatin, large cytoplasmic droplets, coiled altered axonemes, and aberrant acrosomes [Figure 3] and [Figure 4].
Figure 3: Transmission electron microscopy analysis of normal and cryptorchid spermatozoa. (a) Longitudinal section of spermatozoa from control man presents 13–14 mitochondrial gyres in a regular arrangement. Longitudinal sections of spermatozoa from cryptorchid men manifesting (b and c) partly packaged, (d) unpackaged mitochondrial gyres and (b and d) aberrant mitochondria in large cytoplasmic droplet. Note the nuclei with an uncondensed chromatin in b and c, (c) partly detached nuclear envelope (asterisk), or (b) those (arrow) forming swirling invaginations into the cytoplasm, and (d) seemingly acephalic spermatozoon. (e) Cross-section passing through the connecting piece/midpiece of spermatozoon reveals both intact and damaged mitochondria (arrowhead) gyred around the correct axoneme. a: acrosome; ra: reacted acrosome; m: mitochondria; am: aberrant mitochondria; n: nucleus; si: swirling invaginations.

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Figure 4: Transmission electron microscopy analysis of cryptorchid spermatozoa reveals autophagic vacuoles. (a) Longitudinal section of cryptorchid spermatozoon, exhibiting the nucleus with uncondensed chromatin, partly detached nuclear envelope (arrow), and coiled axoneme (ca). The large cytoplasmic droplet contains the autophagic vacuoles (arrowheads), located next to irregular gyres of damaged mitochondria (m). (b) A higher magnification of the selected area from a. Note double membrane-limited autophagic vesicles (arrowheads) containing partly degraded vesicular material. Cross-sections of cryptorchid spermatozoa pass through the postequatorial segment of the heads, which manifest (c) chromatin rarefaction and (e) granulation. (e) Coiled aberrant axonemes (ca) and the fragments of segmented columns (sc) forming conico-cylindrical sleeve are scattered in the cytoplasm. (d) Double-membrane-limited autophagosomes (arrowheads) filled with vesicular material locate in close proximity to (c) the nucleus, (e) while partly degraded mitochondria (asterisk) are next to plasma membrane and seemingly fusion with it. d and f are higher magnifications from selected area from c and e, respectively showing (d) double membrane-limited autophagosomes (arrowhead) enclosing vesicles or (f) mitochondria. m: mitochondria; n: nucleus.

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The midpiece of cryptorchid spermatozoa did not present regularly arranged mitochondria. While in control specimens, mitochondria were approximately equal in size and regularly arranged [Figure 3]a, in cryptorchid specimens they had a more disordered arrangement and showed more variation in size [Figure 3]b, [Figure 3]c, [Figure 3]d, [Figure 3]e. In rare cases, acephalic spermatozoa with abnormally large mitochondria were also detected [Figure 3]d. In contrast to control [Figure 3]a, in cryptorchid sperm, a large body of mitochondria were scattered in cytoplasmic droplets without forming the gyres around the axoneme [Figure 3]b, [Figure 3]c, [Figure 3]d). The asymmetry of mitochondrial gyres with an increased number of mitochondria was also detected [Figure 3]e. In overall, mitochondria from patients with cryptorchid history often looked swollen [Figure 3]d and partly disorganized [Figure 3]b and [Figure 3]c compared to the control [Figure 3]a.

We often detected double-membrane-limited vacuoles in large cytoplasmic droplet in cryptorchid spermatozoa, close to disorganized mitochondrial gyres [Figure 4]a and [Figure 4]b. By morphological criteria, these vacuoles corresponded to autophagosome vesicles. We also detected autophagosomes in close proximity to aberrant nuclei in sections passing through postequatorial segments of sperm head [Figure 4]c and [Figure 4]e. The content of autophagic vacuoles was heterogeneous, so that some of these vacuoles were filled with partly degraded vesicular material [Figure 4]b, [Figure 4]c, [Figure 4]d, others contained the remnants of mitochondria [Figure 4]e and [Figure 4]f. On the contrary, we never observed double-membrane-limited autophagosome vesicles in the sperm cells from control patients.

Collectively, TEM data are in agreement with immunofluorescence (IF) analysis, manifesting activation of autophagy in cryptorchid spermatozoa. To our knowledge, we reveal for the first time the presence of autophagosomes filled with heterogeneous content in human cryptorchid spermatozoa.


  Discussion Top


Here, we show for the first time an increased status of autophagy in sperm cells from cryptorchid patients, probably related to testis hyperthermic conditions. Autophagy is involved in spermatogenesis.[35],[36],[37] Autophagosomes are detected in cultured rat spermatocytes.[38] In mouse germ cells, heat stress induces autophagy in addition to apoptosis.[39] Moreover, exposition of ejaculates to elevated temperature also increases autophagy in human sperm.[40]

In the present study, the activation of autophagy in the cryptorchid sperm was demonstrated by IF and TEM experiments. Using antibodies against the main autophagy membrane protein LC3-II, we revealed a pronounced immunostaining in the midpiece of the tail in cryptorchid sperm compared to control. Such strong anti-LC3 immunostaining in sperm tail midpiece was also reported after the treatment of ejaculates from normozoospermic patients with bafilomicin A, a drug currently used to assess autophagic flux.[40] Anti-LC3 immunoreactivity was also observed in the acrosome and in the equatorial segment in both patient and control sperms. These data were confirmed by TEM analysis, which discerned numerous double-membrane-limited vacuoles, filled with heterogeneous contents in cryptorchid sperm. Autophagic vacuoles were detected not only in sperm tail midpiece, but also in the sperm head and in cytoplasmic droplets, which were often present in cryptorchid specimens. Of note, no autophagic vacuole was observed in sperm cells from normozoospermic controls. The presence of anti-LC3 immunostaining detected in the acrosome of control specimens could be due to the soluble form of LC3 protein, which is not associated with autophagic vesicles.[19]

Remarkably, the most frequent cargoes enclosed into the autophagosomes from cryptorchid sperm contained partly degraded mitochondria. This attests to the activation of mitophagy – a sort of selective autophagy which specifically targets the aberrant and damaged mitochondria.[41] The p62 protein is a specific adaptor in autophagy/mitophagy;[42] it accumulates when autophagy is inhibited, whereas it is degraded when autophagy is induced.[40] Thus, the undetectable level of p62 in cryptorchid sperm is in good agreement with TEM observations revealing the strong signs of autophagy/mitophagy in cryptorchid specimens.

Increased mitophagy implies a mitochondrial damage in cryptorchid sperm. It agrees with our TEM data, which unveil numerous abnormalities in sperm cell mitochondria. As usual, mitochondria from cryptorchid sperm appear swollen and partly disorganized compared to control ones. Besides, the abnormal assembly of mitochondria around the axoneme, and the asymmetry of mitochondrial gyres were observed [Figure 3]b and [Figure 3]e. Our finding corroborates the study of seminal plasma from cryptorchid stallion,[43] in which abnormal mitochondria were also frequent in sperm cells. Together, these data suggest that sperm mitochondria are particularly vulnerable in cryptorchidism, being the substrate for autophagic degradation.

Because hyperthermic environment in body cavity is considered as the primary factor affecting spermatogenesis in cryptorchid testes,[30],[31],[32] its involvement in mitochondrial damage seems likely. We found no literature information on the temperature resistance of sperm mitochondria. Nevertheless, hyperthermia impairs heart mitochondria, leading to the generation of reactive oxygen species (ROS) in mitochondrial matrix[44] and mitochondrial membrane damage. Interestingly, autophagic vacuoles containing damaged mitochondria have been found in germ cells from heat stressed mouse testes.[39] Data from adipose tissue also support the involvement of mitophagy in regulation of mitochondrial homeostasis during temperature challenge.[45] Thus, the abnormal temperature environment should be among the factors inducing mitochondrial damage and the activation of mitophagy in cryptorchid sperm. Besides, impaired mitochondrial integrity we detected in cryptorchid samples could be related to epididymis anomalies. Indeed, maturation and modification of the outer mitochondrial membrane occur during sperm transit through epididymis; the failure of this process results in asthenozoospermia.[46] Because cryptorchidism is associated with epididymis anomalies,[13],[47] this could provoke the aberrations in mitochondrial structure and integrity we detected by TEM.

Mitochondria are the main source of sperm-produced reactive oxygen species (ROS), which can cause oxidative damage, if produced in an unchecked manner.[48],[49] Remarkably, ROS is known to activate autophagy in vitro.[50] ROS have a pathological effect on male gametes resulting in apoptosis-like phenomenon.[49],[51] Swollen mitochondria are one of the hallmarks of early apoptosis stages in cells,[52] and the disruption of mitochondrial membrane facilitates the release of cytochrome c in cell cytoplasm triggering intrinsic mitochondria-mediated apoptosis.[53]

Mitochondria are considered as a switch between apoptosis and autophagy.[54] Indeed, if the damaged mitochondria are not removed by mitophagy, both membrane potential loss and cytochrome c release can trigger apoptosis.[54] By this way, autophagy counteracts apoptosis, contributing to cell survival. Interestingly, our TEM data did not reveal the signs of late stage apoptotic process, characterized by strongly marginated chromatin[55] in cryptorchid specimens. High incidence of autophagosomes filled with swollen mitochondria implies the involvement of autophagy in the survival of cryptorchid sperm cells.

The defects in sperm mitochondrial ultrastructure[49] are associated with decreased sperm motility in humans.[56],[57] This is in agreement with data from this study, because samples from cryptorchid patients exhibited very poor motility compared to the control [Table 1]. Remarkably, autophagy has been recently demonstrated to influence sperm motility as well. Thus, sperm cells treated with autophagy activators exhibited an increased motility, whereas treatment with autophagy blockers decreased their motility.[40] Therefore, the increased autophagy could be important for maintaining the motility of cryptorchid sperm, even if it remains very poor.

In agreement with literature data,[17],[58] our TEM observations also detected a large amount of immature sperm cells with uncondensed chromatin, large cytoplasmic residues, which sometimes contained an altered axoneme in the specimens from cryptorchid patients. The loss of the majority of the cytoplasm occurs during spermiogenesis concomitantly with the loss of excessive mitochondria inside the residual bodies.[56] As recently demonstrated using ATG7 knock-out mice, this process is tightly regulated by autophagy.[24] Besides, the involvement of autophagy in the elimination of excessive mitochondria was recently demonstrated during gametogenesis in fish.[37] Thus, the presence of autophagosomes with the remnants of mitochondria in cytoplasmic residues might also be interpreted as a lack of timely maturation of cryptorchid sperm.

Collectively, the sperm cells from cryptorchid patients exhibit strong signs of autophagy activation. While aberrant mitochondria were the most frequent cargoes in autophagic vacuoles, the presence of other cargoes inside the autophagosomes indicates the general pattern of activation of degradative autophagy. This may have a positive role in the physiology of cryptorchid sperm, contributing to its viability and motility.


  Authors Contributions Top


MGY carried out study design, execution, analysis of data, and writing/revising the manuscript. A Buschiazzo participated in immunohistochemistry and electron microscopy experiments, analysis of data, and manuscript writing. A Burel and MTL participated in electron microscopy experiments. CP, GJ, and S J recruited the patients and controls, and performed sperm and genetic analysis. BJ participated in study conception and manuscript revision. NB was involved in study conception, data analysis, and manuscript revision. CR is the senior author involved in study conception, data analysis, and manuscript revision. All authors read and approved the final manuscript.


  Competing Interests Top


All authors declare no competing interests.


  Acknowledgments Top


We thank Prof. V Catros and Dr. JC Hervé for critical reading of the manuscript. We thank H2P2 platform and MRIC platform from Rennes University. MGY was welcomed as invited researcher and invited Professor by Universite de Rennes1, CHU de Rennes and INSERM IRSET U 1085. MGY acknowledges the DRC (Direction de la Recherche Clinique du CHU de Rennes). CR acknowledges financial support from Rennes Metropole (AIS 2015) and Agence de BioMédecine. This work was supported by funding from Universite de Rennes1, Institut National de la Santé et de la Recherche Médicale (INSERM) and CHU de Rennes.



 
  References Top

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Virtanen HE, Bjerknes R, Cortes D, Jorgensen N, Rajpert-De Meyts E, et al. Cryptorchidism: classification, prevalence and long term consequences. Acta Paediatr 2007; 96: 611–6.  Back to cited text no. 1
    
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