JVAS announces awards - Four best research articles (one each from basic, production, para-clinical and clinical subjects) and one best short communication will be adjudged for awards each year!!!

Journal of Veterinary and Animal Sciences

Volume: 54 Issue: 1

  • Open Access
  • Research Article

Expression of Angiopoietin 2 in ovarian follicles of crossbred Malabari goat

M.S. Adithian1*, V. Babitha2, R. Uma1, I. S. Sajitha3, and E. S. Navya1

1. Department of Veterinary Biochemistry
2. Department of Veterinary Physiology

3.  Department of Veterinary Pathology

College of Veterinary and Animal Sciences, Mannuthy, Thrissur, 680651, Kerala Veterinary and Animal Sciences University, Kerala, India

*Corresponding author: [email protected] Ph: 9747371653

Year: 2023, Page: 43-52, Doi: https://doi.org/10.51966/jvas.2023.54.1.43-52

Received: July 7, 2022 Accepted: Oct. 11, 2022 Published: March 31, 2023

Abstract

Angiopoietin-2 (Ang-2) is a local ovarian growth factor belonging to the angiopoietin/Tie (tyrosine kinase with Ig and EGF homology domains) signalling pathway, one of the main pathways involved in ovarian follicular angiogenesis. The main objective of this study is to assess the differential protein expression of Ang-2 in the developmental phases of ovarian follicles of crossbred Malabari goats employing an immunohistochemical technique. Ang-2 protein expression was found in all developmental phases of ovarian follicles, including primordial, primary, small, and large antral ovarian follicles. Ang-2 was found in the granulosa cells, theca interna cells, follicular fluid (granulosa cells in the FF), endothelial cells of capillaries and germinal epithelium of the goat ovaries. The Quantitative Method-Percentage Positivity of Ang-2 expression revealed that it was higher in the initial stages of ovarian follicular development and decreased with later stages of follicular development in cross-bred Malabari goats. Moreover, the protein expression of Ang2 was found to be higher in granulosa cells (GC) than in theca interna (TI) cells of antral follicles as evident from the higher staining intensity in GC cells compared to TI cells. It is therefore concluded that the Ang-2 protein expression in ovarian follicular cells decreased with an increase in follicle size and development and based on the combined scores for immunostaining (staining intensity and the number of positive staining cells), the Ang-2 was found to be expressed more in the granulosa cell layer compared to the theca interna cells of the antral follicle in crossbred Malabari goats.

Keywords: Angiopoietin-2 (Ang-2), goat, ovarian follicles, immunohistochemistry, granulosa cells, theca interna, protein expression

References

Abramovich, D., Celin, A.R., Hernandez, F., Tesone, M. and Parborell, F. 2009. Spatiotemporal analysis of the protein expression of angiogenic factors and their related receptors during folliculogenesis in rats with and without hormonal treatment. Reproduction137: 309-320.

Annie, V.R., Lucy, K.M., Ashok, N., Maya, S., Hiron, M.H. and Sathu, T. 2021. Scanning electron microscopic study of ovary and oviduct of crossbred dairy cows with ovarian hypoplasia. J. Vet. Anim. Sci. 52: 187-190.

Chowdhury, M.W.H., Scaramuzzi, R.J., Wheeler-Jones, C.P.D. and Khalid, M. 2010. The expression of angiogenic growth factors and their receptors in ovarian follicles throughout the estrous cycle in the ewe. Theriogenology.73: 856-872.

Christensen, A.C.M., Haresign, W. and Khalid, M. 2014. Progesterone exposure of seasonally anoestrous ewes alters the expression of angiogenic growth factors in preovulatory follicles. Theriogenology. 81: 358-367.

CIRG [Central Institute for Research on Goats]. 2013. ‘Vision 2050.’ (2nd Ed.). Central Institute for Research on Goats, Makhdoom, Farah, Mathura (UP) India.2-5p.

Fraser, H.M., 2006. Regulation of the ovarian follicular vasculature. Reprod. Biol. Endocrinol4: 1-9.

Hayashi, K.G., Acosta, T.J., Tetsuka, M., Berisha, B., Matsui, M., Schams, D., Ohtani, M. and Miyamoto, A. 2003. Involvement of angiopoietin-tie system in bovine follicular development and atresia: messenger RNA expression in theca interna and effect on steroid secretion. Biol. Reprod. 69: 2078–2084.

Hayashi, K.G., Berisha, B., Matsui, M., Schams, D. and Miyamoto, A. 2004. Expression of mRNA for the angiopoietin-Tie system in granulosa cells during follicular development in cows. J. Reprod. Dev. 50: 477–480.

Hazzard, T.M., Molskness, T.A., Chaffin, C.L. and Stouffer, R.L., 1999. Vascular endothelial growth factor (VEGF) and angiopoietin regulation by gonadotrophin and steroids in macaque granulosa cells during the peri-ovulatory interval. Mol. Hum. Reprod. 12: 1115-1121.

Maisonpierre, P.C., Suri, C., Jones, P.F., Bartunkova, S., Wiegand, S.J., Radziejewski, C., Compton, D., McClain, J., Aldrich, T.H., Papadopoulos, N. and Daly, T.J. 1997. Angiopoietin-2, a natural antagonist for Tie2 that disrupts in vivo angiogenesis. Science. 277: 55-60.

Mandriota, S.J. and Pepper, M.S. 1998. Regulation of angiopoietin-2 mRNA levels in bovine microvascular endothelial cells by cytokines and hypoxia. Circ. Res. 83: 852-859.

Mishra, S.R., Parmar, M.S., Yadav, V.P., Reshma, R., Bharati, J., Bharti, M.K., Paul, A., Chouhan, V.S., Taru Sharma, G., Singh, G. and Sarkar, M. 2016a. Expression and localization of angiopoietin family in corpus luteum during different stages of oestrous cycle and modulatory role of angiopoietins on steroidogenesis, angiogenesis and survivability of cultured buffalo luteal cells. Reprod. Domest. Anim. 51: 855-869.

Mishra, S.R., Thakur, N., Somal, A., Parmar, M.S., Yadav, V.P., Bharati, J., Bharti, M.K., Paul, A., Verma, M.R., Chouhan, V.S. and Sharma, G.T. 2016b. Expression and localization of angiopoietin family in buffalo ovarian follicles during different stages of development and modulatory role of angiopoietins on steroidogenesis and survival of cultured buffalo granulosa cells. Theriogenology. 86: 1818-1833.

Müller, K., Ellenberger, C. and Schoon, H.A., 2009. Histomorphological and immunohistochemical study of angiogenesis and angiogenic factors in the ovary of the mare. Res. Vet. Sci. 87: 421-431.

Nishigaki, A., Okada, H., Tsuzuki, T., Cho, H., Yasuda, K. and Kanzaki, H. 2011. Angiopoietin 1 and angiopoietin 2 in follicular fluid of women undergoing a long protocol. Fertility and sterility. 96: 1378-1383.

Nishitha, K., Rahmaan, S.B., Shiji, S.S., Sajitha, I.S. and Babitha, V. 2020. Differential expression of angiopoietin-1 in ovarian follicles of cross bred malabari goats by immuno-histochemical method. J. Pharm. Innov. 9: 07-12.

Rani Alex, K.C. and Mercey, K.A. 2010. Prediction of body weight of Malabari goats from body measurements under field conditions. J. Vet. Anim. Sci. 41: 21-27.

Saju, S.S., Plakkot, B. and Babitha, V. 2020. Expression of angiopoietin-1 (ANPT-1) gene in different categories of ovarian antral follicles in tropical goats. J. Pharm. Innov. 9: 235-238.

Shimizu, T., Berisha, B., Schams, D. and Miyamoto, A. 2007. Expression of Angiopoietin (ANPT)‐1, ANPT‐2 and their Receptors in Dominant Follicles during Periovulatory Period in GnRH‐Treated Cow. Reprod. Domest. Anim.42: 221-224.

Shimizu, T., Iijima, K., Sasada, H. and Sato, E. 2003. Messenger ribonucleic acid expressions of hepatocyte growth factor, angiopoietins and their receptors during follicular development in gilts. J. Reprod. Dev. 49: 203–211.

Vakkala, M., Paakko, P. and Soini, Y. 1999. Expression of caspases 3, 6 and 8 is increased in parallel with apoptosis and histological aggressiveness of the breast lesion. Br. J. Cancer. 81: 592-599.

Zhang, L., Yang, N., Park, J.W., Katsaros, D., Fracchioli, S., Cao, G., O’Brien-Jenkins, A., Randall, T.C., Rubin, S.C. and Coukos, G. 2003. Tumor-derived vascular endothelial growth factor up-regulates angiopoietin-2 in host endothelium and destabilizes host vasculature, supporting angiogenesis in ovarian cancer. Cancer Res. 63: 3403-3412.

Cite this article

Adithian,M.S., Babitha,V., Uma,R., Sajitha,I.S. and Navya,E.S. 2023. Expression of Angiopoietin 2 in ovarian follicles of crossbred Malabari goat. J. Vet. Anim. Sci. 54(1):43-52

DOI: https://doi.org/10.51966/jvas.2023.54.1.43-52

Views
208
Downloads
55
Citations