Journals / Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi / 2000 / Cilt: 1 - Sayı: 2

Effects of activation of CD30 signaling pathway on CD30+ cutaneous anaplastic large cell lymphoma cell lines

CD30 İletişim yolu aktivasyonunun CD30+ anaplastik büyük hücreli deri lenfoması hücre serilerine etkileri

Pages
33–37
Publication Date
2022-10-10
DOI
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AI Summary & Key Takeaways

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

These results suggest that TGF-b may interact with the CD30 signaling pathway in the pathogenesis of cutaneous ALCL.

📌 3 Key Takeaways

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Objective & Hypothesis:CD30 activation has pleiotropic effects on different cell lines representing CD30+ lymphomas.
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Key Findings & Data:In nodal T-cell anaplastic large cell lymphomas (ALCL), CD30 activation causes cytolysis and decreased proliferation while in Hodgkinís disease there is either no change or proliferation depending on the cell lines.
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Conclusion & Impact:These results suggest that TGF-b may interact with the CD30 signaling pathway in the pathogenesis of cutaneous ALCL.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

CD30 activation has pleiotropic effects on different cell lines representing CD30+ lymphomas. In nodal T-cell anaplastic large cell lymphomas (ALCL), CD30 activation causes cytolysis and decreased proliferation while in Hodgkinís disease there is either no change or proliferation depending on the cell lines. Mac-1 and Mac-2A are two clonally related cutaneous CD30+ anaplastic large cell lymphoma cell lines developed from early(Mac-1) and advanced (Mac-2A) disease from the same patient. Mac-1 is sensitive to transforming growth factor-b (TGF-b) mediated growth inhibition while Mac-2A is resistant. Both cell lines secrete an activated form of TGF-$beta$. Our aim was to investigate the effects of CD30 activation on Mac cell lines. Methods: To understand the effects of CD30 activation, Mac cell lines were incubated with a CD30 agonistic antibody (HeFi-1). 3H-thymidine incorporation, tumor necrosis factor receptor associated factor 1 (TRAF1) expression and nuclear factor-kB activity was determined. Results: Mac-1 and Mac-2A showed increased proliferation with HeFi-1 while the nodal ALCL cell lines were inhibited. When Mac-1 cells were incubated with HeFi-1 and TGF-b neutralizing antibody, the proliferative rate markedly increased compared to HeFi-1 only.TGF $beta$ resistant cell line Mac-2A did not show the same increase Mac-1 and Mac-2A had activation of NF-kB binding activity and increased expression of TRAF1 in response to CD30 activation by HeFi-1. Significance: This is the first demonstration of functionality of the CD30 signaling pathway in cutaneous CD30+ ALCLs. Autocrine TGF-b secreted from Mac-1 cells partially inhibits the proliferative signal from CD30 activation. These results suggest that TGF-b may interact with the CD30 signaling pathway in the pathogenesis of cutaneous ALCL.

Özet

Amaç: CD30 aktivasyonu çeşitli CD30+ lenfoma hücre kültürleri üzerinde farklı etkilere sahiptir; nodal T hücreli CD30+ anaplastik büyük hücreli lenfoma hücrelerinde proliferasyon hızında azalmaya ve sitolize, Hodgkin lenfoması hücre kültürlerinde ise proliferasyona yol açar. Mac-1 ve Mac-2A aynı hastanın erken ve geç evre CD30+ cilt lenfomasından elde edilmiş hücre kültürü serileridir. Bu iki hücre serisi klonal olarak ilişkilidir. Mac-1 hücre serisinin büyümesi transforming growth factor-beta (TGF-b) tarafından inhibe edilebilmektedir. Mac-2A ise TGF-b tarafından inhibe edilememektedir. Bu hücre serilerinin CD30 aktivasyonuna nasıl yanıt verdikleri bilinmemektedir. Yöntem: CD30 aktivasyonunun Mac hücre serilerinin büyüme özelliklerine etkilerini araştırmak amacıyla hücreler CD30 aktive edici antikor HeFi-1 ile inkübe edilmiş, 3H-thymidine inkorporasyonu, Tümör nekrozis faktör reseptör assosiye faktör (TRAF1) ekspresyonu ve nükleer faktör-bB (NF-kB) aktivitesi değerlendirilmiştir. Bulgular: Mac-1 ve Mac-2A HeFi-1 ile inkübasyon sonucu artmış bir proliferatif yanıt göstermişlerdir. Kontrol olarak kullanılan nodal anaplastik büyük hücreli lenfoma hücreleri ise büyüme inhibisyonu göstermişlerdir. Mac-1 hücreleri HeFi- ve TGF-b nötralize edici antikorla inkübe edildiklerinde, proliferatif yanıt tek başına HeFi-1 inkübasyonuna oranla ciddi şekilde artmıştır. TGF-b'ya rezistan hücre kültürü Mac-2A ise aynı yanıtı göstermemiştir. Mac-1 and Mac-2A HeFi-1 aracılığıyla CD30 aktivasyonuna NF-kB nükleer bağlanma aktivitesi artımı ve artmış TRAF1 ekspresyonu ile yanıt vermiştir. Sonuç: Bu çalışma CD30+ anaplastik büyük hücreli deri lenfomalarında CD30 iletişim yolunun işlevselliğinin gösterildiği ilk çalışmadır. Mac-1 hücrelerinden otokrin salınan TGF-b CD30 aktivasyonundan doğan proliferatif yanıtı kısmen inhibe etmektedir. Bu sonuçlar TGF-b nın CD30 iletişim sistemi ile interaksiyonu olduğunu ve bunun CD30+ deri lenfomaları patojenezinde bir rol oynayabileceğini de düşündürmektedir.

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Cite This Article

LEVİ, E., KADIN, M. E., PFEIFER, W. M. (2022). Effects of activation of CD30 signaling pathway on CD30+ cutaneous anaplastic large cell lymphoma cell lines. Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, Cilt: 1 - Sayı: 2, 33–37. https://ajindex.com/articles/429175

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