Name: Extraction and Analysis of DNA from the Cellular Component of the Eye Humor
Uploaded: 2024-01-12T12:55:00
Description: Watch this Scientific Journal Video about Extraction and Analysis of DNA from the Cellular Component of the Eye Humor at JoVE.com

extraction and analysis of dna from the cellular component of the eye humor

Hücresiz DNA Kullanılarak Vitreoretinal Lenfoma Tanısı

Vitreoretinal lymphoma (VRL) is an aggressive lymphoma associated with primary central nervous system diffuse large B-cell lymphoma1,2,3. VRL is typically fatal due to its involvement in the central nervous system1,2. Although rare1,4, VRL often presents with symptoms similar to posterior uveitis and other vitreoretinal diseases4,5. Consequently, patients exhibiting uveitis symptoms require a diagnosis to either confirm or rule out VRL.
Recently, consensus criteria for diagnosing VRL were published, which involve a combination of clinical examination and laboratory findings6. Specimens commonly used to diagnose VRL include vitreous humor and, more recently, aqueous humor7. Vitreous humor is obtained through a surgical procedure called pars plana vitrectomy, which allows access to the posterior segment of the eye8.
In the presented protocol, both aqueous humor and vitreous humor specimens were collected for cellular and cfDNA extraction. After anesthetizing the patients and placing trocars approximately 4 mm from the corneal limbus, an aqueous humor sample of approximately 100-200 &#181;L was obtained using a 1 mL tuberculin syringe at the corneal limbus. For pseudophakic patients, undiluted vitreous was obtained by introducing sterile air into the infusion, enabling the collection of a larger amount of undiluted vitreous (up to 3.5 mL). In phakic patients, approximately 500 to 1000 &#181;L of undiluted vitreous was removed before turning on an infusion of balanced salt solution. In some cases, secondarily diluted vitreous (500 to 2,000 &#181;L) was collected by switching the infusion to fluid and placing the vitrector within the vitreous skirt to obtain this sample. The most dilute vitreous fraction was collected by preserving the cassette bag (Supplemental Figure 1) at the end of the surgery. Once this bag reached the pathology department, dilute vitreous was obtained from draining fluid out of this bag into conical tubes for subsequent DNA extraction.
Cytopathology of vitreous fluid is often considered the gold standard9. However, several studies have demonstrated limited sensitivity due to processing and minimal cellularity10,11,12. Flow cytometry can aid in identifying clonal B-cells but can also be limited by low cellularity and the fragility of large lymphoma cells13,14,15. Both cytopathology and flow cytometry requires intact whole cells. Many of these cells are destroyed during collection, storage, and processing. When molecular testing is performed using DNA extracted from intact cells (cellular DNA), it suffers from this same limitation. In addition, dividing the limited vitreous specimen for all of these tests reduces the amount of material available for each test.
Cell-free DNA (cfDNA) represents another source of DNA that does not require intact cells. cfDNA from vitreous specimens has been used for the detection of VRL16,17 as well as uveal melanoma18. In this protocol, cellular and cell-free DNA are extracted from vitreous and aqueous fluid to detect VRL.

Yazar Spotlight: Vitreus Mizahından Hücresiz DNA Ekstraksiyonu Kullanarak VRL Teşhisini İlerletme 

Vitreoretinal Lenfoma Tanı ve İzlemi için Vitreus ve Sulu Mizah Örneklerinin Hücresiz DNA Ekstraksiyonu

With this research, we are attempting to use molecular testing of vitreous humor collected from the eye by vitrectomy to diagnose vitreoretinal lymphoma or VRL, which is an aggressive disease whose symptoms overlap those of common inflammatory ocular conditions. Cytopathology flow cytometry and molecular testing are current methods used to diagnose VRL. Published sensitivities of non molecular methods are 44 to 90%for cytopathology and 50 to 60%for flow cytometry, cytopathology, flow cytometry and molecular testing with cellular DNA requires intact neoplastic cells.That poses a problem in vitreous humor specimens because the volume and cellularity of these specimens is low and cells can be degraded by apoptosis as well as specimen collection, processing and storage. We found that cell-free DNA extracted from vitreous fluid specimens provides another source of DNA from molecular testing that does not require intact cells, and that also shows evidence of VRL and can be used to diagnose this lymphoma. Cell-free DNA extraction offers molecular testing without intact neoplastic cells.This allows maximizing the utility of vitreous specimens as intact cells can be reserved for cytopathology and flow cytometry while utilizing the remaining supernatant fluid that would otherwise be discarded for molecular testing.

Watch this Scientific Journal Video about Extraction and Analysis of DNA from the Cellular Component of the Eye Humor at JoVE.com

Extraction and Analysis of DNA from the Cellular Component of the Eye Humor  

Göz Mizahının Hücresel Bileşeninden DNA Ekstraksiyonu ve Analizi

DNA ekstraksiyonunu gerçekleştirmek için önce göz mizahından elde edilen hücre peletine uygun miktarda hücre lizis solüsyonu ekleyin. İyice karıştırmak için çözeltiyi yukarı ve aşağı pipetleyin. Hücreler tamamen parçalandıktan sonra, toplam hacmin üçte birini oluşturmak için bir protein çökelti çözeltisi ekleyin.Şimdi, girdap yapın ve 20 ila 30 saniye kuvvetlice karıştırın. Daha sonra oda sıcaklığında 3000 g'da üç dakika döndürün. Bu arada, 300 mikrolitre izopropanolü temiz bir mikrosantrifüj tüpüne aktarın.Santrifüjleme tamamlandıktan sonra, süpernatanı izopropanol içeren tüpe dikkatlice pipetleyin. Daha sonra, tüpe 1,5 mikrolitre glikojen ekleyin ve iyice karıştırmak için tüpü ters çevirin. DNA çökelmesini kolaylaştırmak için tüpü eksi 20 santigrat derecede bir saat veya gece boyunca bir dondurucuya koyun.Dondurulduktan sonra, tüpü oda sıcaklığında 3000 g'da beş dakikada santrifüjleyin. Ardından, izopropanolü pipetleyin. Peletleri yıkamak için 0,5 mililitre% 70 etanol ekleyin.Eşit yıkamayı sağlamak için tüpü hafifçe ters çevirin. Daha sonra tüpü oda sıcaklığında 3000 g'da bir dakika döndürün. Süpernatanı santrifüj tüpünden atın.Şimdi, çözeltiyi boşaltmak ve peleti kurutmak için tüpü temiz gazlı bez üzerinde ters çevirin. Mikrosantrifüjde hızlı bir dönüşten sonra, kalan etanol damlacığını pipetlemek için ince uçlu tek kullanımlık bir pipet ucu kullanın. Daha sonra, kurutulmuş DNA peletine 45 mikrolitre DNA hidrasyon çözeltisi ekleyin.Ardından tüpü 50 santigrat dereceye ayarlanmış bir ısıtma bloğuna yerleştirin. Göz sıvılarının hem hücresel hem de hücresiz bileşenlerinin DNA verimleri benzerdi. Vitreoretinal lenfoma ile ilişkili bir mutasyonun hücresel ve hücresiz bileşenlerinin PCR analizi yapıldı.Hücresiz bileşende, düşürülmüş bir döngü eşiği ile gösterildiği gibi daha yüksek bir mutasyon oranı mevcuttu.

Research

JoVE Journal

Cancer Research

Extraction and Analysis of DNA from the Cellular Component of the Eye Humor

Cell-Free DNA Extraction of Vitreous and Aqueous Humor Specimens for Diagnosis and Monitoring of Vitreoretinal Lymphoma

Vitreoretinal lymphoma (VRL) represents an aggressive lymphoma, often categorized as primary central nervous system diffuse large B-cell lymphoma. To ...