» Articles » PMID: 28651344

Uterine Responses to Early Pre-attachment Embryos in the Domestic Dog and Comparisons with Other Domestic Animal Species

Overview
Journal Biol Reprod
Date 2017 Jun 28
PMID 28651344
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

In the dog, there is no luteolysis in the absence of pregnancy. Thus, this species lacks any anti-luteolytic endocrine signal as found in other species that modulate uterine function during the critical period of pregnancy establishment. Nevertheless, in the dog an embryo-maternal communication must occur in order to prevent rejection of embryos. Based on this hypothesis, we performed microarray analysis of canine uterine samples collected during pre-attachment phase (days 10-12) and in corresponding non-pregnant controls, in order to elucidate the embryo attachment signal. An additional goal was to identify differences in uterine responses to pre-attachment embryos between dogs and other mammalian species exhibiting different reproductive patterns with regard to luteolysis, implantation, and preparation for placentation. Therefore, the canine microarray data were compared with gene sets from pigs, cattle, horses, and humans. We found 412 genes differentially regulated between the two experimental groups. The functional terms most strongly enriched in response to pre-attachment embryos related to extracellular matrix function and remodeling, and to immune and inflammatory responses. Several candidate genes were validated by semi-quantitative PCR. When compared with other species, best matches were found with human and equine counterparts. Especially for the pig, the majority of overlapping genes showed opposite expression patterns. Interestingly, 1926 genes did not pair with any of the other gene sets. Using a microarray approach, we report the uterine changes in the dog driven by the presence of embryos and compare these results with datasets from other mammalian species, finding common-, contrary-, and exclusively canine-regulated genes.

Citing Articles

Applying a novel kinomics approach to study decidualization and the effects of antigestagens using a canine model†.

De Geyter I, Kowalewski M, Tavares Pereira M Biol Reprod. 2023; 110(3):583-598.

PMID: 38079525 PMC: 10941090. DOI: 10.1093/biolre/ioad170.


Transcriptomic profiling of canine decidualization and effects of antigestagens on decidualized dog uterine stromal cells.

Tavares Pereira M, Kazemian A, Rehrauer H, Kowalewski M Sci Rep. 2022; 12(1):21890.

PMID: 36535952 PMC: 9763427. DOI: 10.1038/s41598-022-24790-6.


Identification of noninvasive diagnostic biomarkers for ectopic pregnancy using data-independent acquisition (DIA)proteomics: a pilot study.

Ma D, Yang R, Chen Y, Huang Z, Shen Y, He C Sci Rep. 2022; 12(1):19992.

PMID: 36411308 PMC: 9678856. DOI: 10.1038/s41598-022-23374-8.


Identification of genetic polymorphisms in unexplained recurrent spontaneous abortion based on whole exome sequencing.

Mou J, Huang S, Yu L, Xu J, Deng Q, Xie Y Ann Transl Med. 2022; 10(10):603.

PMID: 35722368 PMC: 9201170. DOI: 10.21037/atm-22-2179.


Antigestagens Mediate the Expression of Decidualization Markers, Extracellular Matrix Factors and Connexin 43 in Decidualized Dog Uterine Stromal (DUS) Cells.

Kazemian A, Tavares Pereira M, Hoffmann B, Kowalewski M Animals (Basel). 2022; 12(7).

PMID: 35405788 PMC: 8996927. DOI: 10.3390/ani12070798.


References
1.
Gellersen B, Brosens I, Brosens J . Decidualization of the human endometrium: mechanisms, functions, and clinical perspectives. Semin Reprod Med. 2007; 25(6):445-53. DOI: 10.1055/s-2007-991042. View

2.
Aplin J, Charlton A, Ayad S . An immunohistochemical study of human endometrial extracellular matrix during the menstrual cycle and first trimester of pregnancy. Cell Tissue Res. 1988; 253(1):231-40. DOI: 10.1007/BF00221758. View

3.
Norwitz E, Starkey P, Lopez Bernal A . Prostaglandin D2 production by term human decidua: cellular origins defined using flow cytometry. Obstet Gynecol. 1992; 80(3 Pt 1):440-5. View

4.
Ishihara J, Umemoto T, Yamato M, Shiratsuchi Y, Takaki S, Petrich B . Nov/CCN3 regulates long-term repopulating activity of murine hematopoietic stem cells via integrin αvβ3. Int J Hematol. 2014; 99(4):393-406. PMC: 4412171. DOI: 10.1007/s12185-014-1534-x. View

5.
Guillomot M, Guay P . Ultrastructural features of the cell surfaces of uterine and trophoblastic epithelia during embryo attachment in the cow. Anat Rec. 1982; 204(4):315-22. DOI: 10.1002/ar.1092040404. View