Articles
| Open Access | Spatiotemporal Immunohistochemical Profiling and Comparative Analysis of HGF, IGF-I, FGF2, and TGF-α Expression in Goose (Anser anser) Kidney and Liver During Embryonic Hatching and Early Post-Hatch Development
Dr. Chinedu Okafor , Department of Veterinary Anatomy and Wildlife Biology, Faculty of Veterinary Medicine, University of Lagos, Lagos, Nigeria. Dr. Amina Bello , Department of Veterinary Pathology and Wildlife Research, College of Animal Health Sciences, University of Ibadan, Ibadan, Nigeria.Abstract
Embryonic organogenesis in avian species is orchestrated through a tightly regulated network of growth factors that govern cellular proliferation, differentiation, migration, extracellular matrix remodeling, and tissue maturation. Among these regulatory molecules, hepatocyte growth factor (HGF), insulin-like growth factor-I (IGF-I), fibroblast growth factor-2 (FGF2), and transforming growth factor-α (TGF-α) represent fundamental signaling mediators involved in renal and hepatic morphogenesis. Although extensive investigations have characterized these factors in mammalian developmental biology, comparatively limited information is available regarding their spatiotemporal immunohistochemical distribution in geese (Anser anser), particularly during the transition from embryonic hatching to early post-hatch development. This review synthesizes current knowledge regarding the developmental anatomy of avian kidney and liver tissues and critically evaluates the reported localization patterns and biological functions of HGF, IGF-I, FGF2, and TGF-α within embryonic and neonatal stages. Comparative evidence from chickens, ducks, quails, rodents, and humans is integrated to establish mechanistic similarities and species-specific differences in organ maturation. Particular emphasis is placed on the coordinated interactions among these growth factors during nephrogenesis, hepatogenesis, epithelial differentiation, vascularization, and metabolic adaptation immediately following hatching. The review further identifies significant gaps in goose-specific immunohistochemical research and proposes future directions involving quantitative immunohistochemistry, molecular validation, and integrative developmental analyses. Collectively, the available evidence demonstrates that coordinated expression of HGF, IGF-I, FGF2, and TGF-α constitutes an essential regulatory network underlying functional maturation of avian renal and hepatic tissues, thereby providing valuable insights for developmental biology, veterinary histology, comparative anatomy, and poultry science.
Keywords
Goose (Anser anser), immunohistochemistry, HGF, IGF-I
References
Abood DA, Reshag AF, Azhar SK, and Aziz M (2014). Comparative anatomical and histological features of the kidney in Harrier (Circus aueroginosus), chicken (Gallus domesticus) and Mallard duck (Anas platyrhynchos). The Iraqi Journal of Veterinary Medicine, 38(1): 107-113.
Ahmad Alabdallah Z, Norezzine A, Anatolyevich Vatnikov Y, Alekseevich Nikishov A, Vladimirovich Kulikov E, Ravilievna Gurina R, Alexandrovna Krotova E, Il'yasovna Khairova N, Ivanovna Semenova V, Valerievna Magdeeva T et al. (2021). Influence of different genders of Japanese Quail on the functional state of kidneys. Archive of Razi Institute, 76(3): 667-680.
Alison MR, Nasim MM, Anilkumar TV, and Sarraf CE (1993). Transforming growth factor-α immunoreactivity in a variety of epithelial tissues. Cell Proliferation, 26(5): 449-460.
Aslan Ş (2018). Üriner sistem, In: Ş. Aslan (Editor), Kanatlı histolojisi [Poultry histology], Baskı, Dora Yayınevi, Bursa, pp. 85-99. Available at: https://dorayayincilik.com.tr/kitap-kanatli-histolojisi--439.html
Beenken A and Mohammadi M (2009). The FGF family: Biology, pathophysiology and therapy. Nature Reviews Drug Discovery, 8(3): 235-253.
Bingöl SA, Deprem T, İlhan Aksu S, Koral Taşçı S, Ermutlu D, and Aslan Ş (2024). Immunohistochemical localization of leptin and ghrelin in kidney tissue of capsaicin administered diabetic and non-diabetic Rats. Kafkas University Faculty of Veterinary Medicine Journal, 30(3): 341-347.
Bolin G and Burggren WW (2013). Metanephric kidney development in the chicken embryo: Glomerular numbers, characteristics and perfusion. Comparative Biochemistry and Physiology, 166(2): 343-350.
Burgess AW (1989). Epidermal growth factor and transforming growth factor α. British Medical Bulletin, 45(2): 401-424.
Cancilla B, Ford-Perriss MD, and Bertram JF (1999). Expression and localization of fibroblast growth factors and fibroblast growth factor receptors in the developing rat kidney. Kidney International, 56(6): 2025-2039.
Carev D, Saraga M, and Saraga-Babic M (2008). Expression of intermediate filaments, EGF and TGF-α in early human kidney development. Journal of Molecular Histology, 39(2): 227-235.
Carlson MB (2018). Human embryology and developmental biology, 6th Edition, Elsevier Health Science., USA, pp. 318-340, 358-372. Available at: https://books.google.com.tr/books?hl=tr&lr=&id=iyx6DwAAQBAJ&oi=fnd&pg=PP1&dq=human+embryology+carlson+2018&ots=ZDjAF_qX08&sig=_wLtGXaYQVFvddeFp8lC7W7LlU8&redir_esc=y#v=onepage&q=human%20embryology%20carlson%202018&f=false
Choi JW, Kim SW, Kim HS, Kang MJ, Kim SA, Han JY, Kim H, and Ku SY (2024). Effects of melatonin, GM-CSF, IGF-1, and LIF in culture media on embryonic development: Potential benefits of individualization. International Journal of Molecular Sciences, 25(2): 751.
Coppola D, Ouban A, and Gilbert-Barness E (2009). Expression of the insulin-like growth factor receptor 1 during human embryogenesis. Fetal and Pediatric Pathology, 28(2): 47-54.
Çöllü F and Gürcü B (2017). Development of embryonic chick liver and distribution of eNOS, iNOS, laminin α1. Celal Bayar University Journal of Science, 13(2): 311-318.
Davies J (2001). Intracellular and extracellular regulation of ureteric bud morphogenesis. Journal of Anatomy, 198(Pt 3): 257-264.
Defrances MC, Wolf HK, Michalopoulos GK, and Zarnegar R (1992). The presence of hepatocyte growth factor in the developing rat. Development, 116(2): 387-395.
Deprem T, Aksu SI, Taşçi SK, Bingöl SA, Gülmez N, and Aslan Ş (2020). Immunohistochemical distributions of HGF and PCNA in the kidneys of diabetic and non-diabetic mice. Kafkas Üniversitesi Veteriner Fakültesi Dergisi, 26(3): 321-327.
Derynck R (1992). The physiology of transforming growth factor-α. Advances in Cancer Research, 58: 27-52.
Diaz Ruiz C, Asbert M, and Pérez-Tomás R (1996). Immunochemical study of a transforming growth factor-alpha-related protein in the chicken kidney. Kidney International, 49(4): 1053-1063.
Diaz Ruiz C, Perez-Tomas R, Cullere X, and Domingo J (1993). Immunohistochemical localization of transforming growth factor and epidermal growth factor-receptor in the mesonephros and metanephros of the chicken. Cell and Tissue Research, 271(1): 3-8.
Doaa MM, Enas AEH, Hassan AHS, and Fatma A (2013). Histogenesis of liver of Dandarawi chicken. American Journal of Life Science Research, 1(2): 47-58. Available at: https://www.semanticscholar.org/paper/Histogenesis-of-Liver-of-Dandarawi-Chicken-DoaaHassan/f94d9872316bd4735a21976032bee57e498a5b44
Drummond IA, Mukhopadhyay D, and Sukhatme VP (1998). Expression of fetal kidney growth factors in a kidney tumor line: role of FGF2 in kidney development. Experimental Nephrology, 6(6): 522-533.
Erhan F and Ergün L (2018). Comparison of carbohydrate and fat metabolism in bird and mammal liver. Mehmet Akif Ersoy University Journal of Health Sciences Institute, 6(1): 33-42.
Floege J, Eng E, Lindner V, Alpers CE, Young BA, Reidy MA, and Johnson RJ (1992). Rat glomerular mesangial cells synthesize basic fibroblast growth factor. Release, upregulated synthesis, and mitogenicity in mesangial proliferative glomerulonephritis. The Journal of Clinical Investigation, 90(6): 2362-2369.
Gonzalez AM, Buscaglia M, Ong M, and Baird A (1990). Distribution of basic fibroblast growth factor in the 18-day rat fetus: localization in the basement membranes of diverse tissues. The Journal of Cell Biology, 110(3): 753-765.
26. Gurevich E, Segev Y, and Landau D (2021). Growth hormone and IGF1 actions in kidney development and function. Cells, 10(12): 3371.
Download and View Statistics
Copyright License
Copyright (c) 2026 Dr. Chinedu Okafor, Dr. Amina Bello

This work is licensed under a Creative Commons Attribution 4.0 International License.
Authors retain the copyright of their manuscripts, and all Open Access articles are disseminated under the terms of the Creative Commons Attribution License 4.0 (CC-BY), which licenses unrestricted use, distribution, and reproduction in any medium, provided that the original work is appropriately cited. The use of general descriptive names, trade names, trademarks, and so forth in this publication, even if not specifically identified, does not imply that these names are not protected by the relevant laws and regulations.
