Journals / Ankara Üniversitesi Veteriner Fakültesi Dergisi / 2000 / Cilt: 47 - Sayı: 1

Light and electron microscopic studies on the brochus associated lymphoid tissue (BALT) üzerinde ışık ve elektron mikroskobik çalışmalar

Ankara keçilerinin bronşlarla ilişkili lenfoid dokusu (BALT) üzerinde ışık ve elektron mikroskobik çalışmalar

Pages
51–58
Publication Date
2022-10-12
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Lympho-epithelial cells were closely arranged lymphocytes, macrophages and polymorph nuclear leukocytes.

📌 3 Key Takeaways

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Objective & Hypothesis:The purpose of this study was to investigate bronchus-associated lymphoid tissue (BALT) in Angora goats at the light and electron microscopic level.In this study, the samples tissue taken from lung of 10 healthy, 5-6 month-old Angora goats were used as a material.
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Key Findings & Data:It has been observed that the bronchus-associated lymphoid tissue of Angora goats was formed by solitary lymphoid follicles and follicle-associated epithelium (FAE) which covered these follicles.
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Conclusion & Impact:Lympho-epithelial cells were closely arranged lymphocytes, macrophages and polymorph nuclear leukocytes.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

The purpose of this study was to investigate bronchus-associated lymphoid tissue (BALT) in Angora goats at the light and electron microscopic level.In this study, the samples tissue taken from lung of 10 healthy, 5-6 month-old Angora goats were used as a material. It has been observed that the bronchus-associated lymphoid tissue of Angora goats was formed by solitary lymphoid follicles and follicle-associated epithelium (FAE) which covered these follicles. It has been seen that FAE was formed by ci-liated cells and cuboidal lymphoepithelial cells but no goblet cells. Lympho-epithelial cells were closely arranged lymphocytes, macrophages and polymorph nuclear leukocytes.

Özet

Bu çalışma, Ankara keçilerinin bronşlarla ilişkili lenfoid dokusunun (BALT) ışık ve elektron mikroskobik yapısını incelemek amacıyla yapıldı.Çalışmada 10 adet sağlıklı, 5-6 aylık Ankara keçisinin akciğerlerinden alınan doku örnekleri materyal olarak kullanıldı. Ankara keçilerinin bronşlarla ilişkili lenfoid dokusunun, soliter lenf follikülleri ile bu folliküllerin üzerini örten follikülle ilişkili epitelden (FAE) oluştuğu gözlendi. FAE'nin kadeh hücresi içermeyen, silyalı hücreler ve kübik şekilli lenfoepiteliyal hücrelerden oluştuğu gözlendi. Lenfoepiteüyal hücrelerin lenfosit, makrofaj ve polimorf nukleuslu lökositlerle yakın ilişkide olduğu görüldü.

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Cite This Article

KURTDEDE, N., ERGÜN, E., AŞTI, R. N., ERGÜN, L. (2022). Light and electron microscopic studies on the brochus associated lymphoid tissue (BALT) üzerinde ışık ve elektron mikroskobik çalışmalar. Ankara Üniversitesi Veteriner Fakültesi Dergisi, Cilt: 47 - Sayı: 1, 51–58. https://ajindex.com/articles/445404

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References (3)

  1. i.AleksandersenM, Hein WR, LandsverkT, MdureS(I9(0)Distrihuıionof Iymphocyıesuhsetsin thelarKeinıesıınalIymphoid./fı!!iclesof lamhs.Im-Illunology,70, 391-397. 2. AndersonML, MoorePF, HydeDM, DungworthDL (1986) Bronclıusassociated(vmphoidıissue in the unKs of c(ll/Ie:rdatiOlıshiplo (iKi! Res Vet Sci. 41.2 11-220. 3. Aştı RN, KurtdcdeN, ErgünL (1993)KanKalkiı-pekIerininperiferkan T lenlrısiıleriüzerindeışık Vi!dektronmikroskopik~'alışmalar.A Ü Vet Fak Derg.40, 563-576. 4. Aştı RN, TanyotaçA, KurtdcdeN, Özen A (1997)Tve B lenlrısiılerinAnkamkeçilerininIl!Illoiddo-kulanndakidaKtlım/.Türk Vet Hay Derg. 21. 99-105. 5. BianchiATJ, ZwartRJ,.leurissenSHM,Moonen-LcusenHWM(! (92) Dnelopmenıof ıhe B- aııd T-ce!! compartmeııısin porcineIymphoidorgwısImmhirllı /iJ adulı life: an imıııunohisıologıwla[Jproac/ı.Vet Immuno!Immunopathol,33, 20 ı-221 6. RiencnstockJ, BcfusAD (1980)Mucosalıın-munoloKY.Immunology,41. 249-270 7. Bienenstock.I, BefusAD (19H4) Gul- wıd hmııchus.associatedIymphoidıissue.Am J Anal. 170.437-445. 8. Bienenstock.I, JohnstonN (I 976) A /11orpholoKICstudyof rahhiıhronchialIyıııphoidagKrt'gaıesandIymphoepithelium.Lab Invest,35, 343-34H. 9. Rienenstock.I, JohnstonN, PereyDYE(1973)Bronchial1)'lIlphoidıissue.I. Morplıolo
  2. icdıa-mcıeristics.Lab Invesl.2g, 686-692. ıO.BoockmanDE, CoopcrMD (1973)Pylıocy/iJıishı'epitheliumassociaredwiıh Iymphoid./fıIlideıin ıht'hursaof Fahricius.appendix.aııd Peyer's[Jalcheı.AııdeclronlIlicmscopicsıudy.Am J Aual. 136.455-478i I. BöckP (19H9)RoıneiıMikroskopııclıt'Tnhııık.17.Aun. Urbanund Schwarzenberg.Miineheıı.s: 56 ı. 12. ChamberlainDW,NopajaroonsriC, SimonGl'(I 973) Ulımstructureor the pulmoııarvIymphoidıiı-sul'. Am Rev RespirDis, ıOg, 62 i -631. ı3. CormackDH (1987)Hwn 's //isıology.9th edıtion.JB LippincottCompany.Philadelphia. 14. CullingCFA,AllisonRl', Bar Wl' (ı')85) eel/u/iiI'PathologyTechııique.4. edition,Butterworth.London. 15. DobashiM,TerashimaK, Imai Y (1982)Eln:ll"Onmicroscopicstudyor difrerenıiarionor wııi!Jody-producingee!! in mouseIymphnodes(ifıer im-muniwıionwith horserudislıpemxidase.J HistochemCytochem,30, 67-74. 16. EikelenboomP, LevcnbachMGE,Van den BrinkHR, Streefkcrk.lG (1979)Developmenıor T aııd Bcells areilsin peripherulIvmphOldorgwısıır {ht' 1'(/1.Anat Rec. 194, 523-53R 17.Fagerland.lA, Arp LH (1990)A morpholo
  3. ıcııudrofhroııchus-associaıedIymphoidlisıue IIIlurkenAmJAnat.Ig9. 24-34. 18. Fornier:01, Vai F, DcrcnneJPH, ParienteR (1977)BrOlıchiallylııphoepillıelialnodul/-'siıııhe rıl1 AmRevRcspirDis, 11