Placentation and fetal membrane development in the South American coati, Nasua nasua(Mammalia, Carnivora, Procyonidae)
- Phelipe O Favaron†1Email author,
- João C MoriniJr†1,
- Andrea M Mess1,
- Maria A Miglino1 and
- Carlos E Ambrósio2
© Favaron et al.; licensee BioMed Central Ltd. 2014
Received: 8 April 2014
Accepted: 14 June 2014
Published: 27 June 2014
Placental research in carnivores has concentrated on domestic species, which have zonary, labyrinthine placentas with an endotheliochorial barrier. Although the coati, Nasua nasua, is a widely distributed species in South America, data on the development of the placenta and the fetal membranes in this species are very sparse.
Four placentas from mid-gestation to near term were collected from wild individuals and were investigated based on gross morphology, histology, immunohistochemistry and electron microscopy. The available data support the concept that the ancestral condition of placentation in carnivores is phylogenetically characterized by a zonary and labyrinthine placental type with an endotheliochorial fetomaternal barrier, comprising extended epitheliochorial and haemochorial zones, such as hemophagous organs for iron supply and histiotrophe uptake and a yolk sac placenta.
Because of the foundational mechanisms that lead to the considerable complexity of fetomaternal contact zones in carnivores have not been studied, carnivores are interesting animal models for interhaemal barrier differentiation.
KeywordsCarnivore Endotheliochorial placenta Hemophagous organ Yolk sac
The project was approved by the Bioethics Commission of the School of Veterinary Medicine and Animal Science, University of Sao Paulo, Brazil (Protocol Nr. 1598/2009), on July 1st, 2009, and by the Biodiversity Authorization and Information System – SISBIO (Protocol Nr. 21030–1) on September 17th, 2010. The study was performed from July 2009 to November 2011.
In total, four placentas from mid-gestation (n = 2) to near term (n = 2) were collected from 2 wildlife individuals captured in Mangabeiras Park in Belo Horizonte-MG, Brazil. Hemi-ovariohysterectomy was performed following surgical and anesthetic protocols used for domestic carnivores .
Measurements of the occipital-sacral distance of the fetuses’ heads were performed with a stainless-steel caliper, using the nuchal crest at one end and the last sacral vertebra at the opposite end as references (crown-rump, CR), following the methodology proposed by Evans and Sack . The CR distances and the external features of the fetuses were used to estimate the age of each individual. The weight (g) was determined using a digital scale (0.0001 g; BEL Engineering).
After macroscopic examination of the main placental structures (zonary placenta, chorion, allantois, amnion, yolk sac, and hemophagous organs), the tissues were fixed in 4% paraformaldehyde for histology and immunohistochemical staining. The samples were stained for vimentin (1:400, 0.N.602, sc-73259, Santa Cruz Biotechnology, Santa Cruz, CA, USA) to identify mesenchymal cells and endothelium, for cytokeratin (1:300; M0821, Dako, Carpinteria, CA, USA) to identify epithelial and trophoblastic cells, and for proliferating cell nuclear antigen (PCNA; 1:300; PC10, sc-56, Santa Cruz Biotechnology, Santa Cruz, CA, USA) to identify proliferating cells. For this staining, we followed protocols established by our group . The negative control was goat anti-mouse IgG (1:500; AP308F, Chemicon International Temecula, CA, USA). The slides were examined with an Olympus BX40 microscope with a Zeiss KS400 image analysis system. For scanning and transmission electron microscopy, placental samples were fixed in 2.5% glutaraldehyde and processed following established protocols [10, 11].
Macroscopy of the fetuses
The two Nasua nasua offspring displayed CR lengths of 6.3 cm and 6.5 cm at mid-gestation and weighed 21.37 g and 23.88 g. Thus, their estimated age was 37–40 days of pregnancy. Near term (estimated age of 50–53 days of pregnancy), the offspring displayed CR lengths of 8.9 cm and 9.5 cm and weighed 33.61 g and 35.28 g. In both stages, the individuals had a body with distinct cranial, thoracic, and abdominal regions. An elongated and curved tail was also a feature observed in these stages of pregnancy. The forelimbs and hindlimbs were completely formed and presented keratinized claws on the fingers (Figure 1B). On the face, well-formed upper and lower lips were identified. The eyes displayed pigmented retinas. The nasal region was elongated, with several sensorial hair follicles, and the external ear was short but evident (Figure 1C). In addition, the entire body of the fetuses was covered by hair that was short, with dark pigmentation in certain regions, including the face, forelimbs and hindlimbs, and tail (Figure 1B,C).
The placenta and fetal membranes
The chorioallantoic placenta was fully zonary and surrounded each fetus in the abdominal region (Figure 1D). Outside the girdle, the trophoblast of the chorioallantoic membrane was apposed to the vascularized, gland-rich uterus, which had an intact, cubic epithelium (Figure 1E).
The placental girdle in Nasua nasua had a prominent, lamellar labyrinth that was endotheliochorial in nature. Each lobe was supplied by central maternal and fetal vessels in a crosscurrent arrangement (Figure 2A,B). The mesenchyme of the fetal vessels was strongly reactive for vimentin, and it was possible to delimit the maternal and fetal blood systems in the labyrinthine zone (Figure 2C). In contrast, the trophoblast near the maternal vessels was positive for cytokeratin (Figure 2D). The trophoblastic cells close to the fetal blood vessels were especially proliferative, including in the branches of the chorioallantoic membrane near the placental girdle in mid-gestation (Figure 2E,F). Both cellular and syncytiotrophoblasts were frequent in mid-gestation (Figure 2G,H). Near term, the barrier was mainly syncytial and thin, but clustered cytotrophoblasts were present near the fetal vessels (Figure 2B). At that point, the endothelium of the maternal vessels was more hypertrophied than in mid-gestation (Figure 2H). In addition to the main placenta, the coati had a prominent, sac-like, orange area, vascularized by vessels from the umbilical cord that persisted until term (Figure 3A,B). Based on a centrally situated area of destruction allowing leakage of maternal blood, the area emanated into the allantoic cavity (Figure 3B) and was distinct from the labyrinth (Figure 3C). Iron deposits (Figure 3D) indicated a haemophagous nature. Inside, branched, vascularized villi were present, bathed in extravasated maternal blood (Figure 3E). The trophoblast was columnar, with large nuclei, apical vacuoles, and liquid droplets that stored ingested erythrocytes (Figure 3D,E).
Extended non-invasive, non-villous, fetomaternal contact zones similar to what is observed in epitheliochorial placentas are widespread in carnivores [4–21] and are known as the polar zone of the paraplacenta . These zones likely uptake histiotrophe from endometrial glands  and represent an ancient character condition of the group Carnivora. The hyena is unique among carnivores because it presents a hemochorial villous placenta with intimate contact between the fetal and the maternal circulation via so-called intraepithelial capillaries in the syncytial trophoblast . In contrast, true epitheliochorial placentas, serving as main fetomaternal contact zones, i.e., the complete reduction of invasive trophoblasts in maternal tissue interactions into strictly noninvasive forms, are regarded as evolutionarily derived conditions that have occurred in several clades of eutherian mammals, such as the ungulates and relatives [2, 31–34]. Because there is little detailed information on the foundational processes of mammalian trophoblast invasion and its restriction, it is unclear whether the ontogenetic establishment of the carnivore paraplacenta follows similar processes as do the epitheliochorial placentas of close relatives within Laurasiatheria [2, 32]. However, regarding the main fetomaternal exchange region of the placenta, comparative data [4–21] have confirmed that endotheliochorial, labyrinthine placentation belongs to the ancestral carnivore pattern [2, 32]. Within the group, only hyenas have haemochorial placentas [13, 14], which are hemomonochorial in nature, consisting of a continuous layer of syncytial trophoblasts, a basal lamina, and the fetal capillary endothelium .
Regarding the fine structure of the fetomaternal interface, the following characters are widespread among carnivores and seemed to belong to their stem species pattern or ancestral pattern: an endotheliochorial barrier in the zonary or circumferential placenta, in addition to a yolk sac and a large allantoic sac that persist until term. In contrast, the coati and other procyonids were derived from the ancient carnivore condition, maintaining the cellular trophoblast to term [19–21].
Hematomas (hemophagous organs), as specialized quasi-haemochorial zones in addition to the main endotheliochorial placenta, are widespread in carnivores. These structures are usually temporary, are mainly built by phagocytosing cytotrophoblasts [9, 20] that are associated with uterine glands and extravasated blood, serve as the iron supply, and take up histiotrophe [4–21]. Thus, these organs represent multifunctional or heterophagous areas [1, 3, 14]. The ancestral pattern of carnivores likely had such areas at the placental margin, occurring in both Caniformia and Feliformia. Nasua and other Musteloidea [19–21] have large, multilobular organs in a central position. Moreover, Nasua nasua possesses a derived condition in that the organ persists, fully functional, until near term. Areolae are absent in the coati and in other Musteloidae, cats and hyenas [4, 7, 8, 10, 13–21] and likely are not part of the carnivore stem species pattern .
The data on the coati supported previous views on the ancestral placental characters of carnivores; the maintenance of cellular trophoblasts in the barrier and the large, central hemophagous organ that persisted until near term were confirmed. The ancestral pattern of carnivores includes not only an endotheliochorial, labyrinthine placental girdle, but also extended epitheliochorial and hemochorial zones and placental function for the yolk sac. This considerable complexity of fetomaternal contact zones must have evolved before the radiation of carnivores, approximately 65 million years ago [25, 26]. It is currently unclear what types of tissue-specific inflammation patterns and associated molecular mechanisms are involved in establishing specific fetomaternal contact in various regions. Thus, carnivores are interesting animal models for studying the full range of interhaemal barrier differentiation and function within an individual species. The coati may be of special interest to further study persisting hemophagous organs to better understand the nature and functional significance of substance transfer in the placental areas.
We thank Adriana Morini for support in the preparation and laboratory procedures. Financial support was provided by FAPESP (2009/51606-0).
- Enders AC, Carter AM: Comparative placentation: some interesting modifications for histotrophic nutrition – a review. Placenta. 2006, 27 (Suppl): 11-16.View ArticleGoogle Scholar
- Mess A, Carter AM: Evolutionary transformations of fetal membrane characters in Eutheria with special reference to Afrotheria. J Exp Zool B Mol Dev Evol. 2006, 306: 140-163.View ArticlePubMedGoogle Scholar
- Enders AC, Carter AM: The evolving placenta: Convergent evolution of variations in the endotheliochorial relationship. Placenta. 2012, 33: 319-326.View ArticlePubMedGoogle Scholar
- Amoroso EC: Histology of the placenta. Brit Med Bull. 1961, 17: 81-90.PubMedGoogle Scholar
- Anderson JW: Ultrastructure of the placenta and fetal membranes of the dog. I - The placental labyrinth. Anat Rec. 1969, 165: 15-36.View ArticlePubMedGoogle Scholar
- Wynn RM, Corbet JR: Ultrastructure of the canine placenta and amnion. Am J Obstet Gynecol. 1969, 103: 878-887.PubMedGoogle Scholar
- Leiser R, Enders AC: Light- and electron-microscopic study of the near-term paraplacenta of the domestic cat. Act Anat. 1980, 106: 312-326.View ArticleGoogle Scholar
- Leiser R, Koob B: Development and characteristics of placentation in a carnivore, the domestic cat. J Exp Zool. 1993, 266: 642-656.View ArticlePubMedGoogle Scholar
- Stoffel MH, Gille U, Friess AE: Scanning electron microscopy of the canine placenta. Ital J Anat Embryol. 1998, 103: 291-300.PubMedGoogle Scholar
- Miglino MA, Ambrósio CE, Martins DS, Pfarrer C, Leiser R: The carnivore pregnancy: the development of the embryo and fetal membranes. Theriogenology. 2006, 66: 1699-1702.View ArticlePubMedGoogle Scholar
- Ambrósio CE, Brolio MP, Martins DS, Morini JC, Carvalho AF, Miglino MA: Endometrial alterations, early placentation and maternal fetal interaction in carnivores. Rev Bras Reprod Anim. 2011, 35: 217-228.Google Scholar
- Michel G, Elze K, Seifert S: Zur Embryonalentwicklung des Bären unter besonderer Beachtung des Baues der Plazenta. Zoolog Gart. 1983, 53: 290-294.Google Scholar
- Wynn RM, Amoroso C: Placentation in the spotted hyena (Crocuta crocuta Erxleben), with particular reference to the circulation. Am J Anat. 1964, 115: 327-362.View ArticlePubMedGoogle Scholar
- Enders AC, Blankenship TN, Conley AJ, Jones CJP: Structure of the midterm placenta of the spotted hyena, Crocuta crocuta, with emphasis on the diverse hemophagous regions. Cells Tissues Organs. 2006, 183: 141-155.View ArticlePubMedGoogle Scholar
- Enders AC: Histological observations on the chorio-allantoic placenta of the mink. Anat Rec. 1957, 127: 231-245.View ArticlePubMedGoogle Scholar
- Sinha AA, Mossmann HW: Placentation of the sea otter. Am J Anat. 1968, 119: 521-554.View ArticleGoogle Scholar
- Krebs C, Winter H, Dantzer V, Leiser R: Vascular interrelationships of near-term mink placenta: light microscopy combined with scanning electron microscopy of corrosion casts. Microsc Res Tech. 1997, 38: 125-136.View ArticlePubMedGoogle Scholar
- Pfarrer C, Winther H, Leiser R, Dantzer V: The development of the endotheliochorial mink placenta: light microscopy and scanning electron microscopical morphometry of maternal vascular cats. Anat Embryol. 1999, 199: 63-74.View ArticlePubMedGoogle Scholar
- Creed RFS, Biggers JD: Comparative placentation of the raccon. Am J Anat. 1963, 113: 417-446.View ArticlePubMedGoogle Scholar
- Creed RFS, Biggers JD: Placental haemophagous organs in the Procyonidae and Mustelidae. J Reprod Fertil. 1964, 8: 133-137.View ArticlePubMedGoogle Scholar
- Benirschke K: Coatimundi, Nasua narica yucatanica. 2014, http://placentation.ucsd.edu,Google Scholar
- Beisiegel BM: Notes on the coati, Nasua nasua (Carnivora: Procyonidae) in Atlantic Forest area. Rev Bras Biol. 2001, 61: 689-692.Google Scholar
- Gompper ME, Gittleman JL, Wayne RK: Genetic relatedness, coalitions and social behaviour of White-nosed coatis, Nasua narica. Anim Behav. 1997, 53: 781-787.View ArticleGoogle Scholar
- Gompper ME, Gittleman JL, Wayne RK: Dispersal, philopatry, and genetic relatedness in a social carnivore: comparing males and females. Mol Ecol. 1998, 7: 157-163.View ArticlePubMedGoogle Scholar
- Flynn JJ, Finarelli JÁ, Zehr S, Hsu J, Nedbal MA: Molecular phylogeny of the carnivore (Mammalia): assessing the impact of increased sampling on resolving enigmatic relationships. Syst Biol. 2005, 54: 317-337.View ArticlePubMedGoogle Scholar
- Nyakatura K, Bininda-Emonds ORP: Updating the evolutionary history of Carnivora (Mammalia): a new species-level supertree complete with divergence time estimates. BMC Biol. 2012, 10: 12-PubMed CentralView ArticlePubMedGoogle Scholar
- Henning W: Phylogenetische systematic. 1982, Berlin: PareyGoogle Scholar
- Oliveira FS, Toniollo GH, Machado MRF, Paura D: Hemi-ovariossalpingo-histerectomia em pacas prenhes e posterior ocorrência de prenhez (Agouti paca, Linnaeus, 1766). Ciênc Rural. 2003, 33: 547-551.View ArticleGoogle Scholar
- Evans HE, Sack WO: Prenatal development of domestic and laboratory mammals: growth curves, external features and selected references. Anat Histol Embryol. 1973, 2: 11-45.View ArticleGoogle Scholar
- Favaron PO, Carter AM, Ambrosio CE, Morini AC, Mess AM, Oliveira MF, Miglino MA: Placentation in Sigmodontinae: a rodent taxon native to South America. Reprod Biol Endocrinol. 2011, 9: 55-PubMed CentralView ArticlePubMedGoogle Scholar
- Mess A, Carter AM: Evolution of the placenta during the early radiation of placental mammals. Comp Biochem Physiol A Mol Integr Physiol. 2007, 148: 769-779.View ArticlePubMedGoogle Scholar
- Wildman DE, Chen C, Erez O, Grossman LI, Goodman M, Romero R: Evolution of the mammalian placenta revealed by phylogenetic analysis. Proc Natl Acad Sci. 2006, 103: 3203-3208.PubMed CentralView ArticlePubMedGoogle Scholar
- Eliot MG, Crespi BJ: Placental invasiveness mediates the evolution of hybrid inviability in mammals. Am Nat. 2006, 168: 114-120.View ArticleGoogle Scholar
- Capellini I, Venditti C, Barton RA: Placentation and maternal investment in mammals. Am Nat. 2011, 177: 86-98.View ArticlePubMedGoogle Scholar
- Oduor-Okelo D, Neaves WB: The chorioallantoic placenta of the spotted hyena (Crocuta crocuta Erxleben): an electron microscopic study. Anat Rec. 1982, 204: 215-222.View ArticlePubMedGoogle Scholar
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