- Open Access
Placentation in the anteaters Myrmecophaga tridactyla and Tamandua tetradactyla (Eutheria, Xenarthra)
© Mess et al.; licensee BioMed Central Ltd. 2012
- Received: 5 September 2012
- Accepted: 16 November 2012
- Published: 30 November 2012
Since Xenarthra are serious candidates for being basal to Eutheria, their characteristics, e.g. the placental system, influence perceptions of evolution. However, in the subgroup containing the anteaters, data are very limited. The present study aims to elucidate the nature of the feto-maternal interface in the anteater placenta and to interpret these data within an evolutionary context.
Placentas of two species were investigated with histology, immunohistochemistry and transmission electron microscopy.
Remnants of the maternal vessel endothelium were absent, resulting in a fully haemochorial barrier throughout the placenta. Two structurally different parts, the villous and trabecular areas were complex and intermingled. In particular, the trabeculae which consisted of cellular, proliferative trophoblast, associated with connective tissue, were attached to the decidua. The villi contained fetal capillaries and hypertrophied mesenchymal cells that occured near the surface near the end of gestation. The surface of the villi consisted of flat, syncytial trophoblast, interspersed with proliferative trophoblast cells.
Based on fundamental differences between anteaters and armadillos, we inferred that placental evolution was more complex than previously thought. The haemochorial pattern of anteaters was likely an ancient condition of xenarthrans. Consequently, villous placentation may be attributed, at least in part, by convergent evolution, but was also characterized by some features that were widespread among xenarthrans.
- Interhaemal barrier
- Villous placenta
Xenarthra is a group of eutherian mammals that evolved in South America since the mid Paleocene and subsequently radiated successfully [1–3]. Three distinct groups evolved: Cingulata comprises armadillos (Dasypodidae), Pilosa include sloths (Bradypodidae and Megalonychidae) and anteaters (Vermilingua: Myrmecophagidae and Cyclopedidae) [4–6]. The latter had a specialized, elongated rostrum, prominent claws and long gestation periods; they were solitary, crepuscular and inhabited grasslands and other habitats of Central South America [7–10]. Xenarthra represents a supraordinal clade of Eutheria. Since they are serious candidates for being basal to Eutheria [11–13], their character conditions influence perceptions of eutherian evolution . In particular, placental characters vary among xenarthrans [15–19]. Placentation has been well characterized in armadillos [20–26]; they have villous and haemochorial placentas formed by a peculiar, partly invasive interaction with maternal vessels [25–27]. In contrast sloths have lobulated, labyrinthine and endotheliochorial placentas [28–30]. Anteaters are regarded as being similar to armadillos. Consequently, an armadillo-like pattern is regarded to represent the ancient condition of Xenarthra, resulting in evolutionary transformations on the stem lineage of sloths . However, data on anteater placentation are limited to an early stage  and delivered placentas  of the giant anteater Myrmecophaga tridactyla, approximately 10 stages from early- to mid-gestation of the lesser anteater Tamandua tetradactyla as well as a single, late stage of the two-toed anteater Cyclopes didactyla. Important aspects are unresolved, i.e. the degree of trophoblast invasion, development and fine structure of the trabecular area, contribution of fetal or maternal tissues to them as well as the presence or absence of cellular trophoblast in the villi at term . The objective of the present study was to use histology, immunohistochemistry and transmission electron microscopy to characterize similarities and differences among xenarthrans and to interpret these data in an evolutionary context.
Material from Myrmecophaga tridactyla, acquired from a road-killed animal in Brazil, represented mid gestation (approximately 100–110 days [36, 37]). Three delivered placentas were obtained from the breeding group at Dortmund Zoo, Germany. A near-term stage from Tamandua tetradactyla that was more advanced than those described by Becher  was derived from the zoological park in Ilha Solteira, Brazil. This research was approved by the Ethical Committee at the Faculty of Veterinary Medicine and Animal Science of the University of Sao Paulo.
Histology and immunohistochemistry
Material for histology, fixed in 10% formalin in 0.1 M phosphate buffer or Bouin’s solution, was embedded in paraplast, sectioned at 5 μm in an automatic microtome (Leica RM 2155, Nussloch, Germany), and stained with haematoxylin and eosin, Masson’s trichrome, toluidine blue and the periodic acid Schiff reaction (PAS). Immunohistochemistry (for details see [26, 38]) for vimentin was done to detect mesenchymal cells, including remnants of the maternal endothelium and stromal decidua (mouse monoclonal anti-human antibody; RTU-VimV9; 1:300; Novacastra; Wetzlar, Germany), α-smooth muscle actin that similarly labeled vessel walls (1:400; Clone 1A4; Dako Cytomation; Carpinteria, California, USA), cytokeratin to identify epithelial tissues including trophoblast (rabbit polyclonal antibody; wide spectrum screening N1512; 1:100; Dako) and as proliferation marker a mouse monoclonal antibody to human anti-PCNA (proliferation cell nuclear antigen; clone PC10; 1:300; Sigma; St. Louis, USA). Sections were subjected to endogenous peroxidase blockage, non-specific binding was blocked , incubated with the primary antibodies overnight at 4°C in a humid chamber, and rinsed in PBS. A biotinylated secondary antibody and streptavidin-HRP (Dako) were applied for 30 min each, followed by rinsing with PBS. Detection was done with Fast Red TR/Naphthol AS-MX (F4523, Sigma) or DAB and substrate chromogen system (Dako) for 2 min, counterstained with haematoxylin and eosin and mounted in Faramont® (Dako). Negative controls used a goat anti-Mouse IgG (AP308F, 1:500;Chemicon International Temecula, California, USA) in lieu of primary antibody. Slides were examined with an Olympus BX40 microscope with Zeiss KS400 image analysis system.
Transmission electron microscopy
Samples for TEM were fixed in 2.5% glutaraldehyde in cacodylate buffer, post-fixed in 2% phosphate-buffered osmium tetroxide at ph 7.4 for 2 h, embedded in Spurr’s Resin and sectioned with an automatic ultramicrotome (Ultracut R, Leica). Semi-thin sections (400 nm) were stained with toluidine blue. Ultrathin sections (90 nm) were contrasted with 2% uranyl acetate and 0.5% lead citrate and studied in an electron microscope (Morgagni 268D, FEI Company, The Netherlands; Mega View III camera, Soft Imaging System, Germany).
Myrmecophaga tridactyla: mid gestation placenta
Myrmecophaga tridactyla: term placentas
Tamandua tetradactyla: late gestation or near-term placenta
Major aspects of placentation fundamentally differed between anteaters and armadillos. Consequently, an armadillo-like pattern could not be regarded as an ancient condition of xenarthrans. In particular, the feto-maternal interface in anteaters was haemochorial without remnants of the maternal vessel endothelium along the trabeculae. Confirmation derived by application of immunohistochemistry and transmission electron microscopy supported previous hypotheses that during early gestation, the trophoblast is fully invasive throughout the placenta [32, 34], independent of a sinusoid area of maternal vessels present deep inside the uterus in an early stage of Tamandua. In contrast, developing villi in armadillos entered maternal blood sinuses and enlarged them, leaving the endothelium largely intact. Fetal tissues developed inside these sinuses . Since anteaters and armadillos differed from each other as well as in comparison to sloths that had an endotheliochorial type of the barrier [28–30]), the evolutionary courses of placentation among xenarthrans were difficult to establish. However, the pattern manifest in anteaters likely represented an ancient condition, because haemochorial placentation was widespread in eutherian mammals, or may even belong to their stem species pattern [15–19]. Consequently, the unique pattern of haemochorial villous areas and endotheliochorial blood sinuses may be the result of evolutionary transformations on armadillo stem lineage.
Secondly, the depth of trophoblast invasion in anteaters was less than in armadillos. Trophoblast cells invaded the surface of the decidua; only in Tamandua were larger parts of the decidua resorbed (own results, [31–34]), but the fetal tissues did not reach deeply into the myometrium as in armadillos [20–26]. A relatively superficial invasion occurred also in sloths, where syncytial trophoblast was present along endometrial vessels [28–30]. Consequently, trophoblast invasion in the last common ancestor of xenarthrans seemed to be restricted to the endometrium and deciduas, whereas the very deep invasion in armadillos was attributed to a subsequent evolutionary transformation.
However, anteaters and armadillos also shared important similarities (own results, [20–27, 32–35]), i.e. a placental establishment at the fundic region of the uterus, the relatively extended to disc-like placental shape, complex intermingled trabecular and villous areas, dominance of cellular trophoblast with some connective tissue in the trabeculae, syncytiotrophoblastic and partly thin surface of the villi with interspersed trophoblast cells towards the interior, the location of fetal capillaries near the surface of the villi in association to hypertrophied mesenchymal cells, and presence of proliferating trophoblast at the tips of the villi. Due to the widespread distribution of these features within xenarthrans, they likely represented ancient character conditions of the group.
The present study addressed anteater placentation, namely trophoblast invasion and the nature of the feto-maternal interface, and provided new insights regarding the course of evolution of placental characters among xenarthrans. There were fundamental differences between anteaters and armadillos. In particular, maternal endothelium was completely absent throughout the placenta, which was restricted to the endometrium and decidua. This pattern was more likely to be ancient for xenarthrans than the unique mixture of haemochorial and endotheliochorial areas in armadillos. Thus, the villous placenta may have been established by convergent evolution. However, we identified a number of shared similarities that likely were part of the xenarthran stem species pattern. In conclusion, an armadillo-like pattern should not be regarded as ancient condition of xenarthrans, because their placental evolution was more complex than previously established.
This project was supported by CNPq and FAPESP. We thank members of the University of Sao Paulo, Brazil, for technical support. We warmly thank Rose and John Kastelic for help with the English.
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