Journals / Kafkas Üniversitesi Veteriner Fakültesi Dergisi / 2010 / Cilt: 16 - Sayı: 3

Tavuk nöral tüp kapanmasında TGF-βs inhibitör ve aktivatör sisteminin (Smad’s proteinleri) etkilerinin araştırılması

Analysis of the effects of inhibitor and activator systems (Smad’s proteins) of TGF-βs on chick neural tube closure

Pages
437–442
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

In conclusion, the members of TGF-βs are play a role in chick neural tube closure, the secretions of TGF-βs are controlled different Smad proteins.

📌 3 Key Takeaways

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Objective & Hypothesis:The families of TGF-βs and Smads proteins that controls its intracellular signaling pathways are known to play a role in early neurulation.
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Key Findings & Data:The aim of this study is to demonstrate distribution of TGF-βs (1, 2, 3) and Smads (1/2/3, 6, 7) proteins as a system in different hours of neural tube development of chick embryos.
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Conclusion & Impact:In conclusion, the members of TGF-βs are play a role in chick neural tube closure, the secretions of TGF-βs are controlled different Smad proteins.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:civciv embriyoları · civciv · embriyonik gelişim

Abstract

The families of TGF-βs and Smads proteins that controls its intracellular signaling pathways are known to play a role in early neurulation. The aim of this study is to demonstrate distribution of TGF-βs (1, 2, 3) and Smads (1/2/3, 6, 7) proteins as a system in different hours of neural tube development of chick embryos. The SPF eggs were incubated at 37.8±2ºC for $24^{th}$, $30^{th}$, $48^{th}$ , $72^{nd}$ h. After that, embryos were examined using immunohistochemistry and western blotting techniques. To the results, TGFβs immunoreactivities (particularly TGF-β3) at the $24^{th}$, $30^{th}$ and $48^{th}$ h of chick development (during neural tube closure) were determined and decreased at the $72^{nd}$ h (after neural tube closure), but expressions of TGF-βs were detected in all stage of embryos in western blotting. While Smad 1/2/3 immunoreactivitiy and expression was less than that of the Smad 6 and 7 at the $24^{th}$, it was increased at the $30^{th}$ h. Smads proteins immunoreactivities were decresead at the $72^{nd}$ h. In conclusion, the members of TGF-βs are play a role in chick neural tube closure, the secretions of TGF-βs are controlled different Smad proteins. In addition, immunoblotting results showed that TGF-βs and Smads proteins were effective in the development of all tissues and organs of the embryos.

Özet

TGF-β ve onun hücre içi sinyal iletim yolunu kontrol eden Smad protein ailesinin, erken nörülasyonda rol oynadığı bilinmektedir. Bu çalışmanın amacı, tavuk embriyosunda nöral tüp gelişiminin farklı saatlerinde bir sistem olarak TGF-β1,2,3, Smad 1/2/3, 6 and 7 proteinlerinin dağılımını göstermektir. Bunun için, SPF yumurtaları, 24, 30, 48, 72. saatlerde 37.8±2ºC’de inkübe edildi ve sonrasında embriyolar, immunohistokimyasal ve immünoblotting yöntemleriyle incelendi. Elde edilen sonuçlara göre, tavuk gelişiminin 24, 30 ve 48. saatlerinde (nöral tüp kapanması sırasında) TGF-βs immünreaktivitelerinin (özellikle TGFβ3) var olduğu ve 72. saatte (nöral tüp kapanmasından sonra) azaldığı saptanırken western blotting yöntemi ile TGF-βs sentezinin embriyoların tüm dönemlerinde var olduğu gösterildi. Smad 1/2/3 immunreaktivitesi ve sentezi ise 24. saatte Smad 6 and 7’ ninkinden daha az iken 30. saatte daha yüksekti. Sonuç olarak, TGF-β ailesinin, tavuk nöral tüp gelişiminde rol oynadığı ve salınımının farklı Smad proteinleri tarafından kontrol edildiği düşünülmektedir. Bununla birlikte, immünoblotting sonuçlar, TGF-βs ve Smads proteinlerinin embriyonun tüm doku ve organlarının gelişiminde etkili olduğunu göstermektedir.

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Cite This Article

UMUR, N., VATANSEVER, H. S., UMUR, A. Ş., ÖZBİLGİN, M. K., SELÇUKİ, M. (2010). Tavuk nöral tüp kapanmasında TGF-βs inhibitör ve aktivatör sisteminin (Smad’s proteinleri) etkilerinin araştırılması. Kafkas Üniversitesi Veteriner Fakültesi Dergisi, Cilt: 16 - Sayı: 3, 437–442. https://ajindex.com/articles/273277

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References (2)

  1. Smith JL, Schoenwolf GC: Neurulation: Coming to closure. Trends Neurosci, 20, 510-517, 1997 2.Cayuso J, Marti E: Morphogens in Motion: Growth control of the neural tube. J Neurobiol, 64 (4): 376-387, 2005. 3.Larsen WJ: Human Embryology. 2nd ed. pp. 19-106,
  2. New York, Churchill Livingstone, 1997. 4.Dijke PT, Hill C: New insights into TGF-beta/ smad signalling. Trends Biochem Sci, 29 (5): 265-273, 2004. 5.Chang H, Brown CW, Matzuk MM: Genetic analysis of the mammalian transforming growth factor-beta superfamily. Endocr Rev, 23 (6): 787-823, 2002. 6.Massaque J: TGF–beta signal transduction. Annu Rev Biochem, 67, 753-791, 1998. 7.Attisano L, Tuen Lee-Hoeflich S: The Smads. Genome Biol, 2 (8): 3010, 2001. 8.Böttner M, Krieglstein K, Unsicker K: The Transforming Growth Factor-β: Structure, signaling and roles in nervous system development and functions. J Neurochem, 75 (6): 22272240, 2000. 9.Gomes FCA, Sousa VO, Romao L: Emerging roles for TGFβ1 in nervous system development. Int J Dev Neurosci, 23 (5): 413424, 2005. 10.Lawrence DA: Transforming growth factor beta: A General review. Eur Cytokine Netw, 7 (3): 363-374, 1996. 11.Flanders KC, Lüdecke G, Engels S, Cissel DS, Roberts AB, Kondaiah P, Lafyatis R, Sporn MB, Unsicker K: Localization and actions of transforming growth factor- beta in the embryonic nervous system. Development, 113 (1): 183-191, 1991. 12.Unsicker K, Meier C, Krieglstein K, Sartor BM, Flanders KC: Expression, localization and function of transforming growth factor- betas in chick spinal cord, hind brain and dorsal root ganglia. J Neurobio, 29, 262-276, 1996. 13.Unsicker K, Strelaus J: Functions of transforming growth factor- beta isoforms in nervous system. Eur J Biochem, 267, 6972-6975, 2000. 14.Krieglstein K, Rufer M, Suter-Crazzolara C, Unsicker K: Neural functions of the transforming growth factors beta. Int J Dev Neurosci, 13, 301-315, 1995. 15.Sanders E, Hu N, Wride M: Expression of TGFβ1/β3 during early chick embryo development. Anat Res, 238, 397-406, 1994. 16.Hamburger V, Hamilton HL: A series of normal stages in the development of the chick embryo. J Morph, 88, 49-92, 1951. 17.Ergun G, Aktas S: Comparisons of sum of squares methods in ANOVA models. Kafkas Univ Vet Fak Derg, 15 (3): 481-484, 2009. 18.Faure S, De Santa Barbara P, Roberts DJ, Whitmann M: Endogenous patterns of BMP signaling during early chick development. Dev Biol, 244 (1): 44-65, 2002. 19.Pratt BM, Mcpherson JM: TGF-beta in the central nervous system: Potential roles