Madekurozwa_59-65.indd INTRODUCTION Extensive research has been conducted on the inner- vation of the ovary in both birds (Gilbert 1965; 1968; 1969; Unsicker, Seidel, Hofmann, Muller, Schmidt & Wilson 1983) and mammals (Lakomy, Do boszynska & Szteyn 1983; Dees, Hiney, McAr thur, Johnson, Dissen & Ojeda 2006). Early reports described the ovary as being supplied by predominantly sympa- thetic nerves, which form a component of the ovar- ian nerve plexus (Gilbert 1965; 1968; 1969). These sympathetic nerves form part of a neuronal pathway through which the central nervous system exerts a regulatory influence on the ovary (Gerendai, Kocsis & Halasz 2002). The sympathetic nerves supplying the ovary are gen- erally adrenergic in nature. These extrinsic adrener- gic nerves have a myriad of functions, which include the regulation of blood flow (Lakomy et al. 1983), folliculogenesis (Curry, Lawrence & Burden 1984; Kannisto, Owman, Rosengren & Walles 1984), and ovarian steroidogenesis (Weiss, Dail & Ratner 1982; Sporrong, Kannisto, Owman, Sjoberg & Walles 1985; Aguado 2002; Delgado, Sosa, Dominguez, Casais, Aguado & Rastrilla 2004). In addition to the extrinsic sympathetic nerves supplying the ovary, an intrinsic neuronal system has also been identified. The intrin- sic innervation of the ovary is composed of neuronal cell bodies, which are generally catecholiminergic (D’Albora & Barcia 1996; D’Albora, Lombide & Ojeda 2000; Anesetti, Lombide, D’Albora & Ojeda 2001). Although the exact role of ovarian neuronal cell bod- ies is unclear, they are thought to be involved in the inhibition of steroidogenesis and in the regulation of ovarian blood flow (D’Albora, Anesetti, Lombide, Dees & Ojeda 2002). It is clear from the literature that both the extrinsic and intrinsic ovarian innervation is vital to the nor- mal functioning of the ovary. Indeed it has been 59 Onderstepoort Journal of Veterinary Research, 75:59–65 (2008) An immunohistochemical study of ovarian innervation in the emu (Dromaius novaehollandiae) M-C. MADEKUROZWA* Department of Anatomy and Physiology, Faculty of Veterinary Science, University of Pretoria, Onderstepoort, 0110 South Africa ABSTRACT MADEKUROZWA, M-C. 2008. An immunohistochemical study of ovarian innervation in the emu (Dromaius novaehollandiae). Onderstepoort Journal of Veterinary Research, 75:59–65 The present study investigated the distribution of nerves in the ovary of the emu. The neuronal mark- ers, protein gene product 9.5, neurofilament protein and neuron specific enolase demonstrated the constituents of the extrinsic and intrinsic ovarian neural systems. The extrinsic neural system was composed of ganglia in the ovarian stalk, as well as nerve bundles, which were distributed throughout the ovary. Isolated neuronal cell bodies, in the medulla and cortex, formed the intrinsic neural system. An interesting finding of the study was the presence of nerve bundles, circumscribed by lymphocytes, in the ovarian stalk. The findings of the study indicate that the distribution of nerve fibres and neuro- nal cell bodies in the emu ovary is similar, but not identical to that of the domestic fowl and ostrich. Keywords: Emu, immunohistochemistry, innervation, ovary * E-mail: madex@op.up.ac.za Accepted for publication 10 October 2007—Editor 60 Ovarian innervation in the emu (Dromaius novaehollandiae) suggested that ovarian pathologies may result from a dysfunction in innervation (Anesetti et al. 2001; Lara, Dorfman, Venegas, Luza, Luna, Mayerhofer, Guimaraes, Rosa E Silva & Ramirez 2002). To date much of the research conducted on the distribution and function of ovarian nerves has focused on mam- mals (Weiss et al. 1982; Lakomy et al. 1983; Curry et al. 1984; Dees, Hiney, Schultea, Mayerhofer, Danil chik, Dissen & Ojeda 1995; Dees et al. 2006). Furthermore, apart from a recent study conducted on the ovary of the immature ostrich (Kimaro & Ma- dekurozwa 2006), most of the research carried out on birds has been limited to the domestic fowl (Gil- bert 1965; 1968; 1969; Unsicker et al. 1983). Although the emu is an economically important ratite there is currently a lack of information on the ovarian inner- vation of this avian species. The present study de- scribes the distribution of nerve fibres in the ovary of the emu using antibodies against neurofilament pro- tein (NP), protein gene product 9.5 (PGP 9.5) and neuron specific enolase (NSE). Neurofilament pro- tein is expressed specifically in neurons (Ohara, Ga- hara, Miyake, Teraoka & Kitamura 1993), while PGP 9.5 and NSE are cytoplasmic markers of both neu- ronal and neuroendocrine cells (Martin, Fraile, Peina do, Arenas, Elices, Alonso, Paniagua, Martin & San ta maria 2000; Theodoropoulos, Tsigka, Miha- lopoulou, Tsoukala, Lazaris, Patsouris & Ghikonti 2005). MATERIALS AND METHODS A total of eleven female emus aged 18 months and weighing 35–40 kg were used in the present study. The birds originated from a commercial farm in the North West Province of South Africa. All the birds had active ovaries, which contained approximately 30 predominantly yellow-yolk follicles, with the di- ameters of the largest follicles ranging from 20 to 30 mm. The birds were sampled in March. The emu being a short day breeder typically begins to lay in April in the southern hemisphere (Minnaar & Minnaar 1997). The birds were slaughtered at a commercial abat- toir, employing a standard slaughter protocol. Ovari- an tissue samples were obtained from the birds 10–15 min after slaughter. The tissue samples were then immersion-fixed in either 4 % paraformalde- hyde (pH 7.2) or Bouin’s fluid for 12 h. Some sam- ples were fixed in Bouin’s fluid because the antibody against PGP 9.5 reacts better with antigens in par- affin sections. The samples fixed in paraformalde- hyde were then placed for 24 h at 4 °C, in a 30 % sucrose solution made up in 0.01 M phosphate buff- ered saline solution (PBS, pH 7.4). Thereafter, they were snap-frozen in OCT compound (Sakura, CA, USA) in isopentane slurry and then stored at –80 °C. Tissue samples fixed in Bouin’s fluid were proc- essed routinely for histology and embedded in par- affin wax. The immunostaining technique was performed on 10 μm-thick cryostat sections and 5 μm-thick paraf- fin sections, using a LSAB-plus kit (Dakocytomation, Denmark). The cryostat sections were air-dried for 60 min at room temperature after which they were rinsed in PBS. Endogenous peroxidase activity in both cryostat and paraffin sections was blocked, us- ing a 3 % (v/v) hydrogen peroxide solution in water for 5 min. The slides were then rinsed in PBS for 5 min. Thereafter, the paraffin sections were micro- waved at 750 W for two cycles of 7 min each, and after being allowed to cool for 20 min, they were rinsed with PBS and then incubated for 60 min at room temperature in a solution containing a polyclo- nal antibody against PGP 9.5, at a dilution of 1:50. The cryostat sections were incubated for 30 min in a solution containing monoclonal antibodies against NP, at a dilution of 1:25, and a ready-to-use solution of antibodies against NSE, for 60 min. After this in- cubation all tissue sections were rinsed with PBS and then incubated for 15 min in a solution contain- ing a biotinylated secondary antibody (LSAB-plus kit, Dakocytomation, Denmark). Thereafter, the slides were rinsed in PBS and subsequently incubated for 15 min with the streptavidin peroxidase component of the LSAB-plus staining kit. Tissue sections were then rinsed in PBS and bound antibody was visual- ized after the addition of a 3,3’-diaminobenzidine tetrachloride solution (LSAB-plus kit, Dakocyto ma- tion, Denmark). Tissue sections were counterstained with Mayer’s haematoxylin before being dehydrated in graded concentrations of ethanol. In the negative controls the primary antibodies were replaced with either normal mouse or rabbit serum. A histological section of brain tissue was used as a positive control. RESULTS The ovary was composed of an ovarian stalk, me- dulla and cortex. Numerous nerve bundles immuno- positive for NSE, NP and PGP 9.5 coursed through the ovarian stalk and medulla (Fig. 1). Some of the nerve bundles were associated with blood vessels. In addition, a few nerve bundles in the ovarian stalk were closely associated with lymphoid follicles (Fig. 61 M-C. MADEKUROZWA FIG. 1 NP immunoreactive nerve bundles (arrows) in the me- dulla. Some of the nerve bundles are associated with blood vessels (V). Arrowheads: melanocytes FIG. 2 NP immunoreactive nerve bundle (arrows) surrounded by lymphocytes (L) FIG. 3 NP immunonegative neuronal cell bodies (arrows) form a ganglion in the ovarian stalk. Closely associated with the neuronal cell bodies is a NP immunopositive nerve bundle (N) FIG. 4 NSE immunoreactive neuronal cell bodies (arrows) in the medulla. N: nerve bundle FIG. 5 PGP 9.5 immunopositive nerve fibres (arrows) in the upper limits of the cortex. Arrowheads: melanocytes. G: germinal epithelium FIG. 6 Infiltration of an atretic previtellogenic follicle by con- nective tissue stroma (S) and NP immunoreactive nerve fibres (arrows) 62 Ovarian innervation in the emu (Dromaius novaehollandiae) 2). Ganglia, composed of clusters of neuronal cell bodies were present in the ovarian stalk (Fig. 3). The neuronal cell bodies were characterized by the presence of a large round nucleus with a prominent nucleolus. The cytoplasm of these cell bodies was immunopositive for NSE and PGP 9.5, but immu- nonegative for NP. Two to three layers of fibrocytes circumscribed the ganglia. Isolated neuronal cell bodies were demonstrated in the medulla. In some instances the neuronal cell bodies were associated with nerve bundles (Fig. 4). The cortex contained primordial, pre-vitellogenic and vitellogenic follicles. Nerve bundles in the cor- tex were not closely associated with developing pri- mordial and previtellogenic follicles, but rather oc- curred in the connective tissue stroma between the follicles. These cortical nerve bundles branched to form a neural network in the superficial regions of the cortex (Fig. 5). Although nerve fibres were not seen around developing previtellogenic follicles, they were observed in atretic previtellogenic follicles during the infiltration of the follicle by connective tis- sue (Fig. 6). In addition to nerve fibres occasional neuronal cell bodies were observed in the cortex. Vitellogenic follicles were suspended by follicular stalks, which were extensions of the cortex. Several nerve bundles coursed through the follicular stalks and branched to form perifollicular nerve fibres in the superficial tunic and theca externa of the devel- oping vitellogenic follicles (Fig. 7). Most of the peri- follicular nerve fibres were associated with blood vessels. The early stages of atresia in vitellogenic follicles were characterized by the proliferation of theca in- terna and granulosa cells. A neural network was pres ent in the region between the theca interna and granulosa cell layer. The theca interna and granu- losa cells subsequently differentiated into interstitial gland cells, which infiltrated both the theca externa and oocyte. Eventually the interstitial gland cells abutted intramural veins, which were located in the outer limits of the theca externa. At this stage of atre- sia a dense network of nerve fibres was observed between the interstitial gland cells and intramural veins (Fig. 8). The interstitial gland cells eventually dispersed to form stromal interstitial gland cells, which were located in the superficial regions of the cortex. Nerve fibres were observed coursing be- tween the stromal interstitial gland cells. DISCUSSION The neuronal markers used in the study have clear- ly demonstrated the components of both the extrin- sic and intrinsic neural systems of the emu ovary. The extrinsic system was composed of ganglia in the ovarian stalk and nerve bundles in the ovarian stalk, medulla, cortex and follicular stalks. Isolated neuronal cell bodies in the medulla and cortex formed the intrinsic neural system. As in the domestic fowl (Gilbert 1965; 1968; 1969), extrinsic nerve bundles entered the ovary through the ovarian stalk where they subsequently formed a nerve plexus. The ovarian nerve plexus in both the emu and domestic fowl (Gilbert 1965; 1968; 1969; Unsicker et al. 1983) contained several encapsu- lated ganglia. In the present study the nerves form- ing the plexus were immunopositive for NSE, NP FIG. 7 PGP 9.5 immunopositive nerves (arrows) in the theca externa (TE) of a developing vitellogenic follicle. TI: theca interna. G: granulosa cell layer FIG. 8 A network of NSE immunoreactive nerve fibres (ar- rows) is present at the interface between intramural veins (M) and interstitial gland cells (IG) in an atretic vitellogenic follicle 63 M-C. MADEKUROZWA and PGP 9.5, while the ganglia were immunoposi- tive for NSE and PGP 9.5, but immunonegative for NP. In the emu, ostrich (Kimaro & Madekurozwa 2006) and domestic fowl (Gilbert 1965; 1968) nerves in the ovarian stalk coursed into the medulla, cortex and follicular stalks. The role of nerves in blood regulation is well estab- lished (Lakomy et al. 1983). Indeed, the close asso- ciation between nerves and blood vessels has been reported in the ovaries of the rat (Lawrence & Bur- den 1980), domestic fowl (Unsicker et al. 1983), and pig (Lakomy et al. 1983). In the present study, peri- vascular nerve fibres were demonstrated through- out the ovary. Admittedly, the antibodies used pre- cluded the identification of adrenergic and cholinergic nerves. Both cholinergic and adrenergic nerves have been demonstrated in the domestic fowl (Gilbert 1969). However, it was conceded that most of the nerves were adrenergic. This is supported by re- search conducted in the rat in which most perivas- cular nerves are adrenergic (Lawrence & Burden 1980). Although the association between nerves and blood vessels has been extensively reported, the relationship between nerves and lymphoid follicles has received far less attention. An interesting find- ing of the present study was the close association between nerves and lymphoid follicles in the ovarian stalk. Research conducted by Felten, Ackerman, Wiegand & Felten (1987) on the spleen suggests that neurotransmitters released from nerve endings regulate the migration, maturation, proliferation and activation of lymphocytes. The relevance of the close association of nerve bundles and lymphoid follicles in the emu ovary is unclear. The distribution of nerve fibres in the medulla, cor- tex, follicular stalks and perifollicular regions of birds appears to be fairly uniform (Gilbert 1968; 1969; Kimaro & Madekurozwa 2006). Indeed the distribu- tion pattern of perifollicular nerve fibres in the devel- oping follicles of the emu varied little from that of the ostrich (Kimaro & Madekurozwa 2006). In both ra- tites nerves formed a network in the thecal layer. No nerve fibres were seen within the granulosa cell layer. The presence of a thecal neural network and the lack of nerve fibres within the granulosa are con- sistent with observations made in the domestic fowl (Gilbert 1965; 1969). It is thought that in mammals perifollicular nerve fibres play a role in folliculogen- esis (Curry et al. 1984; Kannisto et al. 1984; Mala- med, Gibney & Ojeda 1992) and ovulation (Bahr, Kao & Nalbandov 1974; Luna, Cortes, Flores, Her- nandez, Trujillo & Dominguez 2003). In addition, based on the findings of the present study, it is prob- able that perifollicular nerves are involved in the dif- ferentiation of thecal and granulosa cells into inter- stitial gland cells during atresia. This is evidenced by the presence of numerous nerve fibres in regions of interstitial gland formation in atretic vitellogenic follicles. The presence of a neural network in con- tact with differentiating interstitial gland cells is not surprising, as it has been shown that nerves have a profound effect on the development, maintenance and function of corpora lutea in the bovine (Kotwica, Bogacki & Rekawiecki 2002), pig (Jana, Dzienis, Panczyszyn, Rogozinska, Wojtkiewicz, Skobowiat & Majewski 2005) and rat (Casais, Delgado, Sosa & Rastrilla 2006). In addition to the extrinsic neural system described above, the ovaries of birds and mammals contain an intrinsic neural system. The exact function of the intrinsic neural system is unclear. However, it is thought that this neural system is concerned not only with follicular maturation and blood regulation, but also with the inhibition of steroidogenesis (D’Al- bora et al. 2002). The intrinsic neural system is composed of isolated neuronal cell bodies. As in the domestic fowl (Gilbert 1965; 1968), the neuronal cell bodies in the emu were characterized by the pres- ence of a round nucleus with a prominent nucleolus. Significantly the results of the present study not only confirm the findings of Gilbert (1965; 1968), with re- gard to the morphology of neuronal cell bodies, but also further characterize the physiological nature of these cells. The fact that the neuronal cell bodies were immunopositive for both NSE and PGP sug- gests that they possess a neuroendocrine function. This is supported by research on the rat ovary in which neuronal cell bodies have been shown to pro- duce catecholamines as evidenced by the presence of tyrosine hydroxylase, an enzyme involved in the synthesis of norepinephrine. The distribution and number of neuronal cell bodies appear to be species specific. In the emu a few neu- ronal cell bodies were demonstrated in the medulla and occasionally in the cortex. Likewise, in the os- trich a few neuronal cell bodies were observed in the medulla (Kimaro & Madekurozwa 2006). In con- trast, numerous neuronal cell bodies were observed in the follicular stalks supporting mature follicles in the domestic fowl (Gilbert 1965). In this species very few neuronal cell bodies were observed in the cor- tex or in association with developing follicles (Gilbert 1969). Furthermore no neuronal cell bodies were observed in the medulla. In both the immature os- trich (Kimaro & Madekurozwa 2006) and the emu neuronal cell bodies were occasionally associated 64 Ovarian innervation in the emu (Dromaius novaehollandiae) with nerve bundles. Similar observations have been made in the human ovary where it is thought that the association of neuronal cell bodies with nerve bundles implies a regulatory association between the intrinsic and extrinsic neural systems of the ova- ry (Anesetti et al. 2001). In conclusion, this study has described the salient features of the extrinsic and intrinsic neural systems of the emu ovary. The distribution of nerve fibres in the emu ovary is similar to that of the domestic fowl (Gilbert 1965; 1968; 1969) and ostrich (Kimaro & Ma- dekurozwa 2006). A distinguishing feature of ovari- an innervation in the emu is the close association between nerve bundles and lymphoid follicles in the ovarian stalk. Further research on the significance of this finding needs to be conducted. ACKNOWLEDGEMENTS I thank the technical staff in the University of Pre- toria’s Department of Pathology and Department of Education Innovation (Creative Studios) for their as- sistance. 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