This work was supported by the key projects of Chinese Academy of Sciences (KFZD-SW-205), strategic biological resources technology support system of Chinese Academy of Sciences (CZBZX-1).

이 연구는 유전학과 발달 생물학 연구소의 윤리위원회의 승인을하고, 프로토콜은 인간의 복지를위한 제도적 지침을 따른다. EB 바이러스의 제조 1 <ol><li> 1 일에, 6 mL의 B95-8 세포 배양 해동 완전 RPMI 1640 매체, 10 % 소 태아 혈청, 2 mM L- 글루타민, 항생제 (100 μg의 / ㎖ 스트렙토 마이신, 100 U / ㎖ 페니실린)이 보충 T25 문화 플라스크. 37 ° C에서 5 % CO 2 배양기에서 배양 플라스크를 놓습니다. </li><li> 제 2 일에, 현미경으로 세포의 형태를 관찰한다. 그들은 밝고 라운드 때 세포는 좋은 상태를 유지하고 있습니다. 10 mL의 완전한 RPMI 1640 배지를 추가합니다. </li><li> 하루에 4 일, 10 mL의 신선한 완전한 RPMI 1640 배지를 추가 한 다음 T75 문화 플라스크에 전송할 수 있습니다. </li><li> 하루 8 일, 20 mL의 완전한 RPMI 1640 배지를 추가합니다. </li><li> 즉, 새로운 배지, 기아를 추가하지 않고 팔일의 세포를 유지한다. </li><li> 날 16 일, 세포를 관찰현미경으로 관찰 하였다. 15 mL의 원심 분리 튜브, 12 ㎖ / 튜브에 세포를 수집한다. </li><li> 1 시간 동안 -80 ℃에서 냉동 보존은-하고 빠르게 37 ℃에서 해동. 바이러스 입자가 세포로부터 해제 될 때까지 3 번 반복합니다. </li><li> 실온에서 10 분 동안 240 × g으로 원심 분리기. </li><li> -80 ° C에서 0.22 μm의 필터, 나누어지는 12 ㎖ / 튜브 및 저장소를 통해 뜨는을 필터링합니다. </li></ol> 적혈구 용해 버퍼와 전혈 2. 치료 <ol><li> 15 ㎖의 튜브에 EDTA · K 2 항 응고 0.5 mL의 전혈을 추가합니다. </li><li> 전혈에 (사용 전 0.22 μm의 필터로 여과하고, 실온에서 해동 된) 1 mL의 적혈구 용해 완충액을 넣어 잘 섞는다. 4 분 동안 실온에서 혼합물을 놓는다. 정지 반응에 신속 7 ㎖의 1X PBS - 그럼 5를 추가합니다. </li><li> 실온에서 5 분 동안 240 × g으로 원심 분리기. 백혈구는 튜브의 바닥에 침전된다. </li><li> 상층 액을 버리고, 7 mL의 1640 기본 배지를 추가하여 침전을 씻는다. 실온에서 240 XG에서 5 분 동안 원심 분리기. 두 번 반복합니다. </li><li> (20 % 소 태아 혈청 및 10 μg의 / ㎖의 피토 헤 마글 루티 닌 (PHA)를 함유하는 RPMI 1640 배지) 300 μL 변환 배지에서 세포 펠렛을 재현 탁. </li></ol> 3. EBV 감염 <ol><li> 세포 현탁액에 20 μg의 / ML의 시클로 스포린 A의 60 μL (CSA)를 추가합니다. </li><li> 빠르게 37 ° C에서 EBV의 나누어지는을 녹여. 세포 현탁액 240 μL EBV를 추가합니다. </li><li> 잘 혼합하고 잘 당 96 웰 플레이트에 200 μL를 세포 현탁액을 배치합니다. 증발을 방지 96 웰 플레이트의 주위에 모든 웰에 200 μL 1X PBS를 추가합니다. 37 ° C에서 5 % CO 2 배양기에서 접시를 놓습니다. </li></ol> B-LCLS 4. 확장 및 냉동 보존 <ol><li> EBV 감염 후 첫 달 동안 일주일에 한 번 매체의 절반을 변경합니다. 만 두꺼운 라예세포 조각의 r은 7 일 (그림 2)에서 현미경으로 볼 수 있습니다. EBV 감염 한 달 후에 임파 세포 클러스터는 현미경 (도 2)하에 세포 단편의 두꺼운 층 아래에 표시된다. </li><li> 셀 클러스터는 누가 뭐라고해도 현미경 (그림 2)에서 볼 수 있습니다 때까지 3 일마다 배지의 절반을 변경합니다. 일반적으로이 과정은 10 ~ 20 일이 소요됩니다. </li><li> 혼합 후, 세포를 피펫 팅하고 24 웰 플레이트에 옮긴다. 이 노란색으로 변하면서 완전한 RPMI 1640 배양액의 양을 두 배로. 이 과정은 세포의 성장 속도에 의존한다. </li><li> 이어서, T25 배양 용 플라스크에 세포를 옮긴다. 15ml의 - 매체의 부피가 10로 확장 전까지는 노랑색으로 배양액 부피를 두배. </li><li> 동결하기 전에 매체 24 시간을 변경합니다. 240 × g에서 5 분 동안 원심 분리기 세포 현탁액. FR 10 × 106 / ㎖ - (5)의 농도로 세포 계수기와 함께 동결 세포 개수90 % FBS와 10 % 디메틸 술폭 시드 (DMSO)를 함유하기 Ozen 원액. -80 ° C에 분당 1 ℃의 속도로 고정 후 액체 질소에 직접 전송합니다. </li></ol> 5. 3- (4,5- 디메틸 티아 졸 -2- 일) -2,5- 디 페닐 테트라 졸륨 브로마이드 (MTT) 분석 17 <ol><li> 10 % 소 태아 혈청을 함유하는 배지 1640와 B-LCLS 단일 세포 현탁액을 제조. 잘 위에 96 웰 플레이트 당 종자 3 × 104 세포, 잘 당 100 μL. </li><li> 16 시간 - 12 37 ° C에서 CO 2 배양기 5 %에서 접시를 놓습니다. </li><li> 세포가 성장하는 우물에 MTT (5 ㎎ / ㎖)를 첨가하고, 37 ℃에서 4 시간 동안 빛에 가까이하지 말 것. </li><li> 168 × g으로 10 분 동안 원심 분리기 세포 판. </li><li> 상층 액을 제거하고 잘 당 100 μL DMSO를 추가합니다. 참고 :주의해야합니다. 바늘 모양의 염료 결정을 만지지 마십시오. </li><li> 완전 결정을 용해 저속으로 10 분 동안 플레이트를 흔들어. </li><li> 570 nm의에 의해에서 측정 흡수마이크로 플레이트 분광 광도계. </li></ol>

<ol>
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The authors declare that they have no competing financial interests.

우리는 적혈구 용균 전혈로부터 인간 B 세포를 불멸화하기위한 새로운 방법의 개발을보고하고, B-LCLS은 MTT 분석법으로 평가 하였다 설정된 그것의 세포 생존. 결과 적혈구의 용해 방법에 의해 확립 된 B-LCLS의 세포 생존율은 밀도 구배 분리 방법보다 훨씬 더 높은 것으로 나타났다. 적혈구 용해 방법의 주요 장점은 간단하고 높은 성공률과 높은 세포 생존과 영구 세포주를 확립하기위한 혈액 (0.5ml?...

Resting B cells could be transformed by the Epstein-Barr virus (EBV) in vitro into actively proliferating B lymphoblastoid cell lines (B-LCLs). B-LCLs are similar to germ cells in differentiation and development, and the somatic mutation rate of B-LCLs was only 0.3%1, with negligible genetic and phenotypic alteration. Therefore, B-LCLs, as surrogates for peripheral blood mononuclear cells (PBMCs), have substantially accelerated the progress of genomics, transcriptomics and proteomics study of EBV associated diseases2,3. Moreover, B-LCLs also have important application in screening monoclonal antibodies4,5. 
Several methods have been developed for the immortalization of B lymphocytes by EBV. The most major common procedures include the isolation of B lymphocytes and the use of B95-8 cell lines to produce infectious EBV. From isolation to transformation, these methods are divided into three strategies. Lymphocytes are separated from fresh blood by density gradient centrifugation and EBV transformation directly6-8, named density gradient separation method in this study. However, other techniques overcome the difficulty of shipping fresh blood and use a procedure for freezing purified lymphocytes and subsequent thawing and EBV infection9-11. Cryopreserved whole blood can also be used for the isolation of B lymphocytes and transformation12,13. In addition to density gradient centrifugation to separate B lymphocytes, some researchers use a magnetic cell sorter to select B lymphocytes12. However, magnetic separation is an expensive, complex and time consuming process. Although these methods are useful to immortalize B lymphocytes with a high success rate, the need to treat a large number of clinical samples and the relatively small volume of blood require a simpler method for the establishment of a permanent cell line.
Another less commonly used method is using whole blood as the source of nucleated cells for EBV infection and the establishment of B-LCLs. These methods simplify the technique by omitting the separation procedure. Only a small amount of whole blood, either fresh14 or frozen15,16, is sufficient to obtain the cell lines. Unfortunately, there is great variability in success from documents15,16 and several of our validation tests. Furthermore, transformed colonies are hardly recognized under a microscope because of the large contaminating impurities. Thus, a more reliable method for transformation is required.
Based on the above considerations, we have developed a novel method to establish B-LCLs without previous purification of the lymphocytes, named the red blood cell lysis method. This method is convenient, time saving and applicable to a large number of samples. As little as 0.5 mL of whole blood was enough to obtain B-LCLs that are easily obtainable from infants and the elderly without significantly harming their health.

<table><tbody><tr><td>Centrifuge</td><td>Techcomp</td><td>CT6T</td><td>Centrifugation</td></tr><tr><td>Automated Cell Counter&amp;nbsp;</td><td>Countstar</td><td>&amp;nbsp;IC 1000&amp;nbsp;</td><td>For cell counting&amp;nbsp;</td></tr><tr><td>Epoch Microplate Spectrophotometer</td><td>BioTek Instruments</td><td>SN263839</td><td>For measuring the absorbance</td></tr><tr><td>96 well cell culture cluster</td><td>Corning Incorporated</td><td>3599</td><td>Polystyrene plates</td></tr><tr><td>24 well cell culture cluster</td><td>Corning Incorporated</td><td>3524</td><td>Polystyrene plates</td></tr><tr><td>25 cm&lt;sup&gt;2 &lt;/sup&gt; cell culture flask</td><td>Nest</td><td>707001</td><td>Polystyrene&amp;nbsp;</td></tr><tr><td>FBS</td><td>Gibco</td><td>10270</td><td>Component of B-LCLs medium</td></tr><tr><td>RPMI Medium 1640</td><td>Gibco</td><td>31800-022</td><td>For B-LCLs medium</td></tr><tr><td>L-Glutamine&amp;nbsp;&amp;nbsp;</td><td>Amresco</td><td>0374</td><td>Component of B-LCLs medium</td></tr><tr><td>100x streptomycin penicillin solution BioRoYeeBRY-2309</td><td>BioRoYee</td><td>BRY-2309</td><td>Component of B-LCLs medium</td></tr><tr><td>Ficoll paque plus</td><td>GE&amp;nbsp; Healthcare</td><td>17-1440-03</td><td>For &lt;em&gt;in vitro&lt;/em&gt; isolation of lymphocyte</td></tr><tr><td>PHA-M</td><td>Sigma</td><td>L8902</td><td>For stimulating lymphocyte proliferation</td></tr><tr><td>Cyclosporin A</td><td>Cayman&amp;nbsp; Chemical</td><td>12088</td><td>For inhibiting the cytotoxicity effect of T cells</td></tr><tr><td>Red cell lysis buffer</td><td>Tiangen</td><td>RT122-01</td><td>For lysing red blood cell</td></tr><tr><td>MTT</td><td>Amresco</td><td>0793</td><td>For the detection of cell viability</td></tr><tr><td>DMSO</td><td>Sigma</td><td>D2650</td><td>For freezing cells</td></tr></tbody></table>

a simple red blood cell lysis method for the establishment of b lymphoblastoid cell lines

A number of methods exist for the transformation of B lymphocytes by the Epstein Barr virus in vitro into immortalized cell lines. We have developed a new method with a powerful and simple strategy for the establishment of B-LCLs, the red blood cell lysis method. This method simplified the PBMC separation procedure with red blood cell removal, and used as little as 0.5 mL of whole blood for establishing EBV-immortalized cell lines, which can proliferate to large cell numbers in a relatively short amount time with a 100% success rate. The method is simple, reliable, time saving, and applicable to treating a large number of the clinical samples.

변형 과정에서, 세포의 형태 학적 변화는 광학 현미경 (도 2)에 의해 가시화된다. 세포 파편의 두꺼운 층은 적혈구 세포 용해 방법에서 볼 수있는 반면 작은 셀 클러스터는 감염 후 7 일 후, 밀도 구배 분리법 명확하게 볼 수 있었다. 그러나, 임파 세포 클러스터는 30 일 게시물 감염 세포의 단편의 두꺼운 층 아래에 ​​표시된다. 더 자주 변화 매체로, 세포 파편...

Watch this Scientific Journal Video about A Simple Red Blood Cell Lysis Method for the Establishment of B Lymphoblastoid Cell Lines at JoVE.com

A Simple Red Blood Cell Lysis Method for the Establishment of B Lymphoblastoid Cell Lines

B-LCLS을 설정하기위한 간단한 적혈구 용해 방법은 소량의 혈액을 필요로하고 동결 보존 개시로부터 시간을 절약 불멸화 높은 효율로 발전되었다.

B 임파 세포 라인의 설립에 대한 간단한 적혈구 용해 방법

A number of methods exist for the transformation of B lymphocytes by the Epstein Barr virus in vitro into immortalized cell lines. We have developed a new ...

a-simple-red-blood-cell-lysis-method-for-establishment-b

Universidad de Cartagena UDEC

Research

JoVE Journal

Immunology and Infection

14.8K 조회수.  Chinese Academy of Sciences.  B-LCLS을 설정하기위한 간단한 적혈구 용해 방법은 소량의 혈액을 필요로하고 동결 보존 개시로부터 시간을 절약 불멸화 높은 효율로 발전되었다. 

비디오: A Simple Red Blood Cell Lysis Method for the Establishment of B Lymphoblastoid Cell Lines

Recombinant Retroviral Production and Infection of B Cells

The transgenic expression of genes in eukaryotic cells is a powerful reverse genetic approach in which a gene of interest is expressed under the control of a heterologous expression system to facilitate the analysis of the resulting phenotype. This approach can be used to express a gene that is not normally found in the organism, to express a mutant form of a gene product, or to over-express a dominant-negative form of the gene product. It is particularly useful in the study of the hematopoetic system, where transcriptional regulation is a major control mechanism in the development and differentiation of B cells 1, reviewed in 2-4.
Mouse genetics is a powerful tool for the study of human genes and diseases. A comparative analysis of the mouse and human genome reveals conservation of synteny in over 90% of the genome 5. Also, much of the technology used in mouse models is applicable to the study of human genes, for example, gene disruptions and allelic replacement 6. However, the creation of a transgenic mouse requires a great deal of resources of both a financial and technical nature. Several projects have begun to compile libraries of knock out mouse strains (KOMP, EUCOMM, NorCOMM) or mutagenesis induced strains (RIKEN), which require large-scale efforts and collaboration 7. Therefore, it is desirable to first study the phenotype of a desired gene in a cell culture model of primary cells before progressing to a mouse model. 
Retroviral DNA integrates into the host DNA, preferably within or near transcription units or CpG islands, resulting in stable and heritable expression of the packaged gene of interest while avoiding transcriptional silencing 8 9. The genes are then transcribed under the control of a high efficiency retroviral promoter, resulting in a high efficiency of transcription and protein production. Therefore, retroviral expression can be used with cells that are difficult to transfect, provided the cells are in an active state during mitosis. Because the structural genes of the virus are contained within the packaging cell line, the expression vectors used to clone the gene of interest contain no structural genes of the virus, which both eliminates the possibility of viral revertants and increases the safety of working with viral supernatants as no infectious virions are produced 10. 
Here we present a protocol for recombinant retroviral production and subsequent infection of splenic B cells. After isolation, the cultured splenic cells are stimulated with Th derived lymphokines and anti-CD40, which induces a burst of B cell proliferation and differentiation 11. This protocol is ideal for the study of events occurring late in B cell development and differentiation, as B cells are isolated from the spleen following initial hematopoetic events but prior to antigenic stimulation to induce plasmacytic differentiation.

An efficient system of structure and function analysis of a gene in an ex vivo culture of splenic B-lymphocytes is described. This method takes advantage of recombinant retroviral production in a helper free, ecotrophic packaging cell line. Stable, heritable expression of a gene of interest within primary lymphocytes is achieved leading to generation of surface antibodies on B cells undergoing class switch recombination.

B 세포의 재조합 생산 및 Retroviral 감염

The transgenic expression of genes in eukaryotic cells is a powerful reverse genetic approach in which a gene of interest is expressed under the control ...

연구

면역학 및 감염병학

Establishment of Epstein-Barr Virus Growth-transformed Lymphoblastoid Cell Lines

Infection of B cells with Epstein-Barr virus (EBV) leads to proliferation and subsequent immortalization, resulting in establishment of lymphoblastoid cell lines (LCL) in vitro. Since LCL are latently infected with EBV, they provide a model system to investigate EBV latency and virus-driven B cell proliferation and tumorigenesis1. LCL have been used to present antigens in a variety of immunologic assays2, 3. In addition, LCL can be used to generate human monoclonal antibodies4, 5 and provide a potentially unlimited source when access to primary biologic materials is limited6, 7.
A variety of methods have been described to generate LCL. Earlier methods have included the use of mitogens such as phytohemagglutinin, lipopolysaccharide8, and pokeweed mitogen9 to increase the efficiency of EBV-mediated immortalization. More recently, others have used immunosuppressive agents such as cyclosporin A to inhibit T cell-mediated killing of infected B cells7, 10-12.
The considerable length of time from EBV infection to establishment of cell lines drives the requirement for quicker and more reliable methods for EBV-driven B cell growth transformation. Using a combination of high titer EBV and an immunosuppressive agent, we are able to consistently infect, transform, and generate LCL from B cells in peripheral blood. This method uses a small amount of peripheral blood mononuclear cells that are infected in vitroclusters of cells can be demonstrated. The presence of CD23 with EBV in the presence of FK506, a T cell immunosuppressant. Traditionally, outgrowth of proliferating B cells is monitored by visualization of microscopic clusters of cells about a week after infection with EBV. Clumps of LCL can be seen by the naked eye after several weeks. We describe an assay to determine early if EBV-mediated growth transformation is successful even before microscopic clusters of cells can be demonstrated. The presence of CD23hiCD58+ cells observed as early as three days post-infection indicates a successful outcome.

We describe a method for generating transformed B cell lines using Epstein-Barr virus. We also illustrate a novel assay that can identify B cells destined to undergo transformation as early as three days after infection.

엡스타인 - 바 바이러스 성장 변화 Lymphoblastoid 전지 라인 구축

Infection of B cells with Epstein-Barr virus (EBV) leads to proliferation and subsequent immortalization, resulting in establishment of lymphoblastoid ...

A Chromatin Immunoprecipitation Assay to Identify Novel NFAT2 Target Genes in Chronic Lymphocytic Leukemia

Chronic lymphocytic leukemia (CLL) is characterized by the expansion of malignant B cell clones and represents the most common leukemia in western countries. The majority of CLL patients show an indolent course of the disease as well as an anergic phenotype of their leukemia cells, referring to a B cell receptor unresponsive to external stimulation. We have recently shown that the transcription factor NFAT2 is a crucial regulator of anergy in CLL. A major challenge in the analysis of the role of a transcription factor in different diseases is the identification of its specific target genes. This is of&#160;great significance for the elucidation of pathogenetic mechanisms and potential therapeutic interventions. Chromatin immunoprecipitation (ChIP) is a classic technique to demonstrate protein-DNA interactions and can, therefore, be used to identify direct target genes of transcription factors in mammalian cells. Here, ChIP was used to identify LCK as a direct target gene of NFAT2 in human CLL cells. DNA and associated proteins are crosslinked using formaldehyde and subsequently sheared by sonication into DNA fragments of approximately 200-500 base pairs (bp). Cross-linked DNA fragments associated with NFAT2 are then selectively immunoprecipitated from cell debris using an &#945;NFAT2 antibody. After purification, associated DNA fragments are detected via quantitative real-time PCR (qRT-PCR). DNA sequences with evident enrichment represent regions of the genome which are targeted by NFAT2 in vivo. Appropriate shearing of the DNA and the selection of the required antibody are particularly crucial for the successful application of this method. This protocol is ideal for the demonstration of direct interactions of NFAT2 with target genes. Its major limitation is the difficulty to employ ChIP in large-scale assays analyzing the target genes of multiple transcription factors in intact organisms.

Chronic lymphocytic leukemia (CLL) is the most common leukemia in the western world. NFAT transcription factors are important regulators of development and activation in numerous cell types. Here, we present a protocol for the use of chromatin immunoprecipitation (ChIP) in human CLL cells to identify novel target genes of NFAT2.

만성 림프모구 백혈병에서 소설 NFAT2 대상 유전자를 식별 하는 Chromatin Immunoprecipitation 분석 결과

Chronic lymphocytic leukemia (CLL) is characterized by the expansion of malignant B cell clones and represents the most common leukemia in western ...

암 연구학

Isolation and Activation of Murine Lymphocytes

B and T cells, with their extremely diverse antigen-receptor repertoires, have the ability to mount specific immune responses against almost any invading pathogen1,2. Understandably, such intricate abilities are controlled by a large number of molecules involved in various cellular processes to ensure timely and spatially regulated immune responses3. Here, we describe experimental procedures that allow rapid isolation of highly purified murine lymphocytes using magnetic cell sorting technology. The resulting purified lymphocytes can then be subjected to various in vitro or in vivo functional assays, such as the determination of lymphocyte signaling capacity upon stimulation by immunoblotting4 and the investigation of proliferative abilities by 3H-thymidine incorporation or carboxyfluorescein diacetate succinimidyl ester (CFSE) labeling5-7. In addition to comparing the functional capacities of control and genetically modified lymphocytes, we can also determine the T cell stimulatory capacity of antigen-presenting cells (APCs) in vivo, as shown in our representative results using transplanted CFSE-labeled OT-I T cells.

Lymphocytes are the major players in adaptive immune responses. Here, we present a lymphocyte purification protocol to determine the physiological functions of the desired molecules in lymphocyte activation in vitro and in vivo. The described experimental procedures are suitable for comparing functional capacities between control and genetically modified lymphocytes.

분리 및 쥐 림프구의 활성화

B and T cells, with their extremely diverse antigen-receptor repertoires, have the ability to mount specific immune responses against almost any invading ...

A Fluorescence-based Lymphocyte Assay Suitable for High-throughput Screening of Small Molecules

High-throughput screening (HTS) is currently the mainstay for the identification of chemical entities capable of modulating biochemical reactions or cellular processes. With the advancement of biotechnologies and the high translational potential of small molecules, a number of innovative approaches in drug discovery have evolved, which explains the resurgent interest in the use of HTS. The oncology field is currently the most active research area for drug screening, with no major breakthrough made for the identification of new immunomodulatory compounds targeting transplantation-related complications or autoimmune ailments. Here, we present a novel in vitro murine fluorescent-based lymphocyte assay easily adapted for the identification of new immunomodulatory compounds. This assay uses T or B cells derived from a transgenic mouse, in which the Nur77 promoter drives GFP expression upon T- or B-cell receptor stimulation. As the GFP intensity reflects the activation/transcriptional activity of the target cell, our assay defines a novel tool to study the effect of given compound(s) on cellular/biological responses. For instance, a primary screening was performed using 4,398 compounds in the absence of a &#34;target hypothesis&#34;, which led to the identification of 160 potential hits displaying immunomodulatory activities. Thus, the use of this assay is suitable for drug discovery programs exploring large chemical libraries prior to further in vitro/in vivo validation studies.

We present in the current study a novel fluorescence-based assay using lymphocytes derived from a transgenic mouse. This assay is suitable for high-throughput screening (HTS) of small molecules endowed with the capacity of either inhibiting or promoting lymphocyte activation.

작은 분자의 높은 처리량 스크리닝 적합한 형광 계 분석 림프구

High-throughput screening (HTS) is currently the mainstay for the identification of chemical entities capable of modulating biochemical reactions or ...

Rapid Quantification of Mitogen-induced Blastogenesis in T Lymphocytes for Identifying Immunomodulatory Drugs

Lymphocyte proliferation in response to antigenic or mitogenic stimulation is a readily quantifiable phenomenon useful for testing immunomodulatory (i.e., immunosuppressive or immunostimulatory) chemical compounds and biologics. One of the earliest steps during mitogenesis is cell enlargement or blastogenic transformation, whereupon the cell volume increases before division. It is usually detectable in the first several hours of T-lymphocyte stimulation. Here, we describe a rapid method to quantify blastogenesis in T lymphocytes isolated from mouse spleens and human peripheral blood mononuclear cells (PBMCs) using an automated cell counter. Various commonly used proliferation assays for the most part are laborious and only reflect the overall population effect rather than individual cellular effects within a population. In contrast, the presented automated cell counter assay provides rapid, direct, and precise measurements of cell diameters that can be used for assessing the effectiveness of various mitogens and immunomodulatory drugs in vitro.

T-lymphocyte mitogenesis is accompanied by blastogenic transformation, whereupon the cell volume enlarges before cell division. Here, we describe a method to quantify blastogenesis in T lymphocytes using an automated cell counter with the capability of measuring cell diameters.

면역 마약 식별을위한 T 림프구에서 미토 겐 유도 블라스의 신속한 정량

Lymphocyte proliferation in response to antigenic or mitogenic stimulation is a readily quantifiable phenomenon useful for testing immunomodulatory (i.e., ...

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice

Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical and immunological manifestations. Several spontaneous and inducible animal models mirror common components of human disease, including the bm12 transfer model. Upon transfer of bm12 splenocytes or purified CD4 T cells, C57BL/6 mice rapidly develop large frequencies of T follicular helper cells (Tfh), germinal center (GC) B cells, and plasma cells followed by high levels of circulating anti-nuclear antibodies. Since this model utilizes mice on a pure C57BL/6 background, researchers can quickly and easily study disease progression in transgenic or knockout mouse strains in a relatively short period of time. Here we describe protocols for the induction of the model and the quantitation Tfh, GC B cells, and plasma cells by multi-color flow cytometry. Importantly, these protocols can also be used to characterize disease in most mouse models of SLE and identify Tfh, GC B cells, and plasma cells in other disease models.

The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice

The transfer of bm12 lymphocytes into a C57BL/6 recipient is an established model of systemic lupus erythematosus. Here we describe how to initiate disease using this model and how to characterize T follicular helper cells, germinal center B cells and plasma cells by flow cytometry.

C57BL / 6 마​​우스의 전신 홍 반성 루푸스의 BM12 유도 성 모델 (SLE)

Systemic lupus erythematosus (SLE) is an autoimmune disease with diverse clinical and immunological manifestations. Several spontaneous and inducible ...

의학

An Efficient and Simple Method to Establish NK and T Cell Lines from Patients with Chronic Active Epstein-Barr Virus Infection

A number of methods have been described to establish NK/T cell lines from patients with lymphoma or lymphoproliferative syndrome. These methods employed feeder cells, purified NK or T cells with as much as 10 mL of blood, or a high-dose of IL-2. This study presents a new method with a powerful and simple strategy to establish NK and T cell lines by culturing the peripheral blood mononuclear cells (PBMC) with the addition of recombinant human IL-2 (rhIL-2), and uses as little as 2 mL of whole blood. The cells can proliferate quickly in two weeks and be maintained for more than 3 months. With this method, 7 NK or T cell lines have been established with a high success rate. This method is simple, reliable, and applicable to establishing cell lines from more cases of CAEBV or NK/T cell lymphoma.

A simple method for obtaining NK and T cell clones from CAEBV patients was developed with high efficiency, a small amount of peripheral blood, and a low-dose of IL-2.

NK과 만성 활성 엡 스타인-바 바이러스 감염을 가진 환자에서 T 셀 라인을 설정 하는 효율적이 고 간단한 방법

A number of methods have been described to establish NK/T cell lines from patients with lymphoma or lymphoproliferative syndrome. These methods employed ...

Functional Assessment of Antibody-Secreting B Cells Using ELISpot Assay

Source: Tzeng, S. J. <a href="https://appjove.unicartagenaproxy.elogim.com/v/54582">The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of Humoral Immunity.</a> J. Vis. Exp. (2016)
This video demonstrates the use of the ELISpot assay to assess the function of antibody-secreting B cells, ASCs. The antibodies secreted by the ASCs interact with the membrane-bound polyclonal antibody fragments, which are detected by the enzyme-conjugated IgG or IgM antibodies. The colored spot produced in each well indicates the presence of the specific antibody&#39;s isotype, which correlates with the B cells&#39; secretory activity.

ELISpot Assay를 사용한 항체 분비 B 세포의 기능 평가

Source: Tzeng, S. J. The Isolation, Differentiation, and Quantification of Human Antibody-secreting B Cells from Blood: ELISpot as a Functional Readout of ...

JoVE Encyclopedia of Experiments

Immunology

Immune Systems and Components

Assays and Functional Profiling

An In Vitro Technique to Stimulate Lymphocytes via Pathogenic Bacteria

Source: Dousha, L., et al. <a href="https://appjove.unicartagenaproxy.elogim.com/v/62572">Assessing Respiratory Immune Responses to Haemophilus Influenzae.</a> J. Vis. Exp. (2021)
This video demonstrates an in vitro technique to stimulate lymphocytes via non-typeable Haemophilus influenzae (NTHi) and to assess the immune response. Incubating isolated peripheral blood mononuclear cells (PBMCs) with NTHi causes the bacterial cells to stimulate T lymphocytes, leading to cytokine production. Upon inhibiting the secretion of cytokines, immunofluorescence staining is performed to detect the accumulated intracellular cytokines in stimulated T lymphocytes.

병원성 박테리아를 통해 림프구를 자극하는 체외 기술

Source: Dousha, L., et al. Assessing Respiratory Immune Responses to Haemophilus Influenzae. J. Vis. Exp. (2021)
This video demonstrates an in vitro ...

B 임파 세포 라인의 설립에 대한 간단한 적혈구 용해 방법

요약

더 많은 비디오 탐색

이 비디오의 챕터

B 세포의 재조합 생산 및 Retroviral 감염

엡스타인 - 바 바이러스 성장 변화 Lymphoblastoid 전지 라인 구축

만성 림프모구 백혈병에서 소설 NFAT2 대상 유전자를 식별 하는 Chromatin Immunoprecipitation 분석 결과

분리 및 쥐 림프구의 활성화

작은 분자의 높은 처리량 스크리닝 적합한 형광 계 분석 림프구

면역 마약 식별을위한 T 림프구에서 미토 겐 유도 블라스의 신속한 정량

C57BL / 6 마우스의 전신 홍 반성 루푸스의 BM12 유도 성 모델 (SLE)

NK과 만성 활성 엡 스타인-바 바이러스 감염을 가진 환자에서 T 셀 라인을 설정 하는 효율적이 고 간단한 방법

ELISpot Assay를 사용한 항체 분비 B 세포의 기능 평가

병원성 박테리아를 통해 림프구를 자극하는 체외 기술

B 임파 세포 라인의 설립에 대한 간단한 적혈구 용해 방법

요약

더 많은 비디오 탐색

이 비디오의 챕터

B 세포의 재조합 생산 및 Retroviral 감염

엡스타인 - 바 바이러스 성장 변화 Lymphoblastoid 전지 라인 구축

만성 림프모구 백혈병에서 소설 NFAT2 대상 유전자를 식별 하는 Chromatin Immunoprecipitation 분석 결과

분리 및 쥐 림프구의 활성화

작은 분자의 높은 처리량 스크리닝 적합한 형광 계 분석 림프구

면역 마약 식별을위한 T 림프구에서 미토 겐 유도 블라스의 신속한 정량

C57BL / 6 마​​우스의 전신 홍 반성 루푸스의 BM12 유도 성 모델 (SLE)

NK과 만성 활성 엡 스타인-바 바이러스 감염을 가진 환자에서 T 셀 라인을 설정 하는 효율적이 고 간단한 방법

ELISpot Assay를 사용한 항체 분비 B 세포의 기능 평가

병원성 박테리아를 통해 림프구를 자극하는 체외 기술

C57BL / 6 마우스의 전신 홍 반성 루푸스의 BM12 유도 성 모델 (SLE)