• 제목/요약/키워드: flow cytometry

검색결과 1,241건 처리시간 0.035초

Expanded IL-22+ Group 3 Innate Lymphoid Cells and Role of Oxidized LDL-C in the Pathogenesis of Axial Spondyloarthritis with Dyslipidaemia

  • Hong Ki Min;Jeonghyeon Moon;Seon-Yeong Lee;A Ram Lee;Chae Rim Lee;Jennifer Lee;Seung-Ki Kwok;Mi-La Cho;Sung-Hwan Park
    • IMMUNE NETWORK
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    • 제21권6호
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    • pp.43.1-43.14
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    • 2021
  • Group 3 innate lymphoid cells (ILC3), which express IL-22 and IL-17A, has been introduced as one of pathologic cells in axial spondyloarthritis (axSpA). Dyslipidaemia should be managed in axSpA patients to reduce cardiovascular disease, and dyslipidaemia promotes inflammation. This study aimed to reveal the role of circulating ILC3 in axSpA and the impact of dyslipidaemia on axSpA pathogenesis. AxSpA patients with or without dyslipidaemia and healthy control were recruited. Peripheral blood samples were collected, and flow cytometry analysis of circulating ILC3 and CD4+ T cells was performed. The correlation between Ankylosing Spondylitis Disease Activity Score (ASDAS)-C-reactive protein (CRP) and circulating immune cells was evaluated. The effect of oxidized low-density lipoprotein cholesterol (oxLDL-C) on immune cell differentiation was confirmed. AxSpA human monocytes were cultured with with oxLDL-C, IL-22, or oxLDL-C plus IL-22 to evaluate osteoclastogenesis using tartrate-resistant acid phosphatase (TRAP) staining and real-time quantitative PCR of osteoclast-related gene expression. Total of 34 axSpA patients (13 with dyslipidaemia and 21 without) were included in the analysis. Circulating IL-22+ ILC3 and Th17 were significantly elevated in axSpA patients with dyslipidaemia (p=0.001 and p=0.034, respectively), and circulating IL-22+ ILC3 significantly correlated with ASDAS-CRP (Rho=0.4198 and p=0.0367). Stimulation with oxLDL-C significantly increased IL-22+ ILC3, NKp44- ILC3, and Th17 cells, and these were reversed by CD36 blocking agent. IL-22 and oxLDL-C increased TRAP+ cells and osteoclast-related gene expression. This study suggested potential role of circulating IL-22+ ILC3 as biomarker in axSpA. Furthermore, dyslipidaemia augmented IL-22+ ILC3 differentiation, and oxLDL-C and IL-22 markedly increased osteoclastogenesis of axSpA.

GRIM-19 Ameliorates Multiple Sclerosis in a Mouse Model of Experimental Autoimmune Encephalomyelitis with Reciprocal Regulation of IFNγ/Th1 and IL-17A/Th17 Cells

  • Jeonghyeon Moon;Seung Hoon Lee;Seon-yeong Lee;Jaeyoon Ryu;Jooyeon Jhun;JeongWon Choi;Gyoung Nyun Kim;Sangho Roh;Sung-Hwan Park;Mi-La Cho
    • IMMUNE NETWORK
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    • 제20권5호
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    • pp.40.1-40.15
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    • 2020
  • The protein encoded by the Gene Associated with Retinoid-Interferon-Induced Mortality-19 (GRIM-19) is located in the mitochondrial inner membrane and is homologous to the NADH dehydrogenase 1-alpha subcomplex subunit 13 of the electron transport chain. Multiple sclerosis (MS) is a demyelinating disease that damages the brain and spinal cord. Although both the cause and mechanism of MS progression remain unclear, it is accepted that an immune disorder is involved. We explored whether GRIM-19 ameliorated MS by increasing the levels of inflammatory cytokines and immune cells; we used a mouse model of experimental autoimmune encephalomyelitis (EAE) to this end. Six-to-eight-week-old male C57BL/6, IFNγ-knockout (KO), and GRIM-19 transgenic mice were used; EAE was induced in all strains. A GRIM-19 overexpression vector (GRIM19 OVN) was electrophoretically injected intravenously. The levels of Th1 and Th17 cells were measured via flow cytometry, immunofluorescence, and immunohistochemical analysis. IL-17A and IFNγ expression levels were assessed via ELISA and quantitative PCR. IL-17A expression decreased and IFNγ expression increased in EAE mice that received injections of the GRIM-19 OVN. GRIM19 transgenic mice expressed more IFNγ than did wild-type mice; this inhibited EAE development. However, the effect of GRIM-19 overexpression on the EAE of IFNγ-KO mice did not differ from that of the empty vector. GRIM-19 expression was therapeutic for EAE mice, elevating the IFNγ level. GRIM-19 regulated the Th17/Treg cell balance.

Immunological Characteristics of Hyperprogressive Disease in Patients with Non-small Cell Lung Cancer Treated with Anti-PD-1/PD-L1 Abs

  • Kyung Hwan Kim;Joon Young Hur;Jiae Koh;Jinhyun Cho;Bo Mi Ku;June Young Koh;Jong-Mu Sun;Se-Hoon Lee;Jin Seok Ahn;Keunchil Park;Myung-Ju Ahn;Eui-Cheol Shin
    • IMMUNE NETWORK
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    • 제20권6호
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    • pp.48.1-48.11
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    • 2020
  • Hyperprogressive disease (HPD) is a distinct pattern of progression characterized by acceleration of tumor growth after treatment with anti-PD-1/PD-L1 Abs. However, the immunological characteristics have not been fully elucidated in patients with HPD. We prospectively recruited patients with metastatic non-small cell lung cancer treated with anti-PD-1/PD-L1 Abs between April 2015 and April 2018, and collected peripheral blood before treatment and 7-days post-treatment. HPD was defined as ≥2-fold increase in both tumor growth kinetics and tumor growth rate between pre-treatment and post-treatment. Peripheral blood mononuclear cells were analyzed by multi-color flow cytometry to phenotype the immune cells. Of 115 patients, 19 (16.5%) developed HPD, 52 experienced durable clinical benefit (DCB; partial response or stable disease ≥6 months), and 44 experienced non-hyperprogressive progression (NHPD). Patients with HPD had significantly lower progression-free survival (p<0.001) and overall survival (p<0.001). When peripheral blood immune cells were examined, the pre-treatment frequency of CD39+ cells among CD8+ T cells was significantly higher in patients with HPD compared to those with NHPD, although it showed borderline significance to predict HPD. Other parameters regarding regulatory T cells or myeloid derived suppressor cells did not significantly differ among patient groups. Our findings suggest high pre-treatment frequency of CD39+CD8+ T cells might be a characteristic of HPD. Further investigations in a larger cohort are needed to confirm our results and better delineate the immune landscape of HPD.

A Co-inhibitory Molecule, B7-H4, Synergistically Potentiates Oral Tolerance by Inducing CD4+CD25+FoxP3+ T Cells

  • Wen, Lanying;Yang, Sung-Yeun;Choi, Jae-Kyoung;Kim, Young-Hee;Kwon, Eun-Hee;Lee, Hyun-Ji;Jeoung, Hae-Young;Hwang, Du-Hyeon;Hwang, Dong-Jin;Choi, In-Hak
    • IMMUNE NETWORK
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    • 제8권1호
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    • pp.21-28
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    • 2008
  • Background: A co-inhibitory molecule, B7-H4, is believed to negatively regulate T cell immunity by suppressing T cell proliferation and inhibiting cytokine production. However, the mechanism behind B7-H4-mediated tolerance remains unclear. Methods: Balb/c $(H-2^d)$ mice were fed with dendritic cell line, DC2.4 $(H-2^d)$ every day for 10 days. Meantime, mice were hydrodynamically injected with recombinant plasmid expressing B7-H4 fusion protein (B7-H4.hFc) or hFc via tail vein. One day after last feeding, mice were immunized with allogeneic B6 spleen cells. 14 days following immunization, mice were challenged with B6 spleen cells to ear back and the ear swelling was determined the next day. Subsequently, a mixed lymphocyte reaction (MLR) was also performed and cytokines profiles from the reaction were examined by sandwich ELISA. Frequency of immunosuppressive cell population was assayed with flow cytometry and mRNA for FoxP3 was determined by RT-PCR. Results: Tolerant mice given plasmid expressing B7-H4.hFc showed a significant reduction in ear swelling compared to control mice. In addition, T cells from mice given B7-H4.hFc plasmid revealed a significant hyporesponsiveness of T cells against allogeneic spleen cells and showed a significant decrease in Th1 and Th2 cytokines such as IFN-${\gamma}$, IL-5, and TNF-${\alpha}$. Interestingly, flow cytometric analysis showed that the frequency of CD4+CD25+FoxP3+ Tregs in spleen was increased in tolerant mice given recombinant B7-H4.hFc plasmid compared to control group. Conclusion: Our results demonstrate that B7-H4 synergistically potentiates oral tolerance induced by allogeneic cells by increasing the frequency of FoxP3+ CD4+CD25+ Treg and reducing Th1 and Th2 cytokine production.

간암 세포주에서의 Indole-3-Carbinol에 의해 유도되는 세포주기 억제 기전 (Inhibitory Mechanisms of Cell Cycle Regulation Induced by Indole-3-carbinol in Hepatocellular Carci-noma HepG2 Cells.)

  • 김동우;이광수;김민경;조율희;이철훈
    • 한국미생물·생명공학회지
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    • 제29권3호
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    • pp.181-185
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    • 2001
  • 유방암 세포주에서는 우수한 항암활성을 가진 것으로 알려진 indole-3-carbinol을 HepG2세포주에 시간과 농도별로 처리한 결과 cell growth inhibition을 확인하였으며, $IC_{50}$ 값은 48시간배양에서 $446\mu$M 72시간 배양에서 444$\mu$M로 나타났다. $400\mu$M의 I3C을 투여하고, 24, 48, 72시간에 HePG2 세포주의 cell cycle pattern을 분석한 결과, G1 phase에서 P21의증가와 함께 Cdk 6와 cyclin D의 확연한 감소와 Pb protein의 hypo-phosphorylation을 확인하였다. 반면 G2 phase에서는 I3C의 직접적인 억제로 인해 24시간 후부터 Cdc2와 cyclin B1가 급격히 감소하는것을 확인하였다. Flow cytomery 분석결과 I3C 처리 24시간 뒤 G2 arrest (25%)가 발생하였으며, 72시간이 지난후 G1 arrest (53%)가 발생하였다. 이러한 I3C의 간암세포주인 HePG2 cell의 cell cycle arrest가 apoptosis를 유발하는지를 알고자 caspase 3 Bcl2 Bax protein의 발현양상을 확인한 결과 아무런 변화가 보이지 않았다. 즉 I3C은 간암세포주인 HepG2 cell에서 apoptosis를 유도하지 못한다는것을 확인하였따. 결론적으로 I3C은 HepG2 세포주에서 G1와 G2 phase에서 cell cycle arrest는 발생시키나, 특이적으로 apoptosis 와는 연관되지 않는다는 사실을 확인하였다.

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유육종증의 활동성 지표로서의 ICAM-1 (The Value of ICAM-1 Expression and the Soluble ICAM-1(sICAM-1) Level as a Marker of Activity in Sarcoidosis: The Relationship Between the ICAM-1 Level and the Clinical Course of the Disease)

  • 김동순;백상훈;심태선;임채만;이상도;고윤석;김우성;김원동
    • Tuberculosis and Respiratory Diseases
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    • 제45권1호
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    • pp.116-127
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    • 1998
  • 연구배경: 유육종증은 원인불명의 만성 육아종성병변으로서 전신에 다 생길수 있으나 폐문부 임파절을 위시한 흉곽내에 가장 많이 발생한다. 유육종증의 경과는 다양하여 많은 환자들이 치료없이 자연적으로 치유되나 일부 환자들에서는 병변이 계속진행하여 호흡부전이나 심지어는 사망까지도 초래하지만 어떤 환자가 계속 진행할지를 알려주는 좋은 지표는 아직도 발견되지 못하였다. 최근 염증세포들이 침윤을 위해서는 접착분자들이 활성화된다는 것이 알려짐에 따라 접착분자, 특히 ICAM-1이 이러한 유육종종이 활동성이 지표로 이용될 수 있을 가능성이 제시되었고 본 연구는 이러한 가능성을 확인하기 위하여 유육종증 환자들의 임상양상 및 그 진행경과와 폐포대식세포 AM)에서의 ICAM-1 발현도 및 혈중 가용성 ICAM-1(sICAM-1)농도 변화를 비교분석하였다. 방법 및 대상: 조직검사로 확인된 19명의 폐유육종종환자툴(남자 5명, 여자 14명, 평균 연령 : $39.4{\pm}10.7$세)을 대상으로 하였고, 그 중 7명은 활동성유육종증이었고, 12명은 비활동성 환자들이었다. 진단시 BAL을 시행하여 flow cytomctry로 AM에서의 ICAM-1 발현도를 측정하고, 혈청 및 BAL액내의 sICAM-1 농도를 ELISA 법으로 촉정하였으며, 또한 임상경과중에 혈중 sICAM-1 농도도 측정하였다. 결 과: AM의 ICAM-1 발현도는 활동성환자들에서 (RMFI: $3.68{\pm}1.71$) 비활동성환자들보다 (RMFI: $1.89{\pm}0.75$, P=0.0298) 유의하게 높았고, 혈청 및 BAL 액내 sICAM-1 농도도 활동성 유육종증에서(혈청: $582{\pm}193$ng/ml, BALF: $47.8{\pm}16.5$ng/ml) 비활동성 환자들보다(혈청 : $294{\pm}117$ ng/ml, p=0.0049, BALF: $20.9{\pm}8.3$ ng/ml) 증가되어 있었다. 또한 활동성환자들의 AM의 ICAM-1 발현도 및 (RMFI: $1.51{\pm}0.84$) 혈중 sICAM-1 농도는 steroid치료후 유의하게 감소하였으나($250{\pm}147$ ng/ml), 비활동성 환자들에서는 경과관찰중 유의한 변화는 없었다. 4명의 환자들에서는 부작용으로 steroid를 중지한 후 유육종종이 악화되었는데 이때 혈중 sICAM-1 농도도 같이 증가하였으며 1명에서는 재치료후 증상호전과 함께 sICAM-1농도도 감소하였다. 결 론: 이상의 결과로 미루어 ICAM-1, 특히 혈중 sICAM-1 농도는 유육종증 활성도의 좋은 지표가 될 수 있을 것으로 사료된다.

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2016~2017년 동중국해 북부해역의 초미소식물플랑크톤 분포 특성 (Distribution characteristics and community structure of picophytoplankton in the northern East China Sea in 2016-2017)

  • 박경우;유만호;오현주;윤석현;권기영;문창호
    • 환경생물
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    • 제37권1호
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    • pp.93-108
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    • 2019
  • Synechococcus 속은 전 계절에 출현하였으며, 저수온기에 현존량이 가장 낮았고, 고수온기에 서쪽해역에서 최대 현존량을 나타내었다. 동중국해 북부해역의 서쪽해역에서 Synechococcus 속은 2017년에 비해 장강희석수의 유입량이 많았던 2016년에 현존량이 높게 나타나 고수온과 장강희 석수를 통한 영양염 유입이 Synechococcus 속 성장에 밀접한 관계가 있음을 알 수 있었다. 또한 Synechococcus 속은 동중국해 북부해역의 서쪽해역과 동쪽해역에서 서로 다른 계통군이 존재함을 기존 연구에서도 알 수 있었다(Choi 2012). Picoeukaryotes은 계절적으로 춘계에 현존량이 가장 높았고, 조사시기 동안 Synechococcus 속에 비해서는 현존량이 낮았다. 그러나 picoeukaryotes은 Synechococcus와 Prochlorococcus 속보다 크기가 크고 생체량이 높기 때문에 동중국해 북부해역에서 일차생산자로써 중요한 역할을 할 것으로 판단된다. Prochlorococcus 속은 저수온기인 동계와 춘계에는 출현하지 않았으며, 하계와 추계에는 쿠로시오수의 영향을 받는 동쪽해역에서 제한적으로 분포하였고 수직적으로 유세포 분석기의 형광값 차이에 의해서 형광값이 낮았던 생태형 I과 형광값이 높았던 생태형 II로 구분되어 나타났다. 또한 Prochlorococcus 속은 쿠로시오수의 유입량이 많은 추계에 가장 넓은 범위에서 분포함에 따라 쿠로시오수의 유입량이 생장 및 분포 범위에 영향을 미치는 것으로 판단된다. 이와 같이 동중국해 북부해역에서 Synechococcus와 Prochlorococcus 속의 생장과 분포는 수괴의 영향에 따라 서로 다른 물리 화학적 환경에서 다양한 계통군이 출현하였다. 따라서 동중국해 북부해역의 수괴의 구조를 파악하는데 초미소식물플랑크톤이 유용한 생물학적 지표가 될 수 있으며, 동중국해의 환경 특성 및 이에 연동되는 생태계 특성을 파악하기 위한 유용한 정보를 제공하기 위해서는 분자생물학적 분석이 병행되어야 할 것으로 생각한다.

보존된 동종동맥편 조직의 면역성 변화에 관한 연구 (Changes in Immunogenicity of Preserved Aortic Allograft)

  • 전예지;박영훈;강영선;최희숙;임창영
    • Journal of Chest Surgery
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    • 제29권11호
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    • pp.1173-1181
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    • 1996
  • 동종동맥판의 보존기법이 발전하면서 상당한 정도의 생육성이 보존되며, 특히 면역반응의 주된 요인인 내피세포 생육성이 약 50%이상 보존되기 때문에 보존처리된 동종동맥판 내피세포의 면역능력을 평가하는것이 동종동맥판의 임상적변화의 원인을 규명하는데 필요할 것이다. 실험은 200~250gm의 Sprague-Dawley Rat를 사용하였다. Rat로부터 적출한 동맥벽을 현재 임상적으로 사용하고 있는 냉장보존법과 냉동보존법을 사용하여 2주일간 보존하였으며 보존처리전(No treat)과 멸균처리후(sterile),냉장 보존후 1(1day), 2(2day), 7(7day), 14일째(14day), 2주간의 냉동보존후(cryo)에 표본을 채취하여 보존시간에 따른 변화를 관찰하였다. 면역표현에 대한 연구를 위하여 혈관조직으로부터 내피세포를 분리한 뒤 면역조직화학검사(Immunohistochemical study)를 하였다. 혈관내피세포의 항원 표현정도를 정량적으로 분석하기 위하여 anti-MHC class I antibody(MRC OX-18)과 anti-MHC class II antibody(MRC OX-6), anti-ICAM antibody를 사용하였다. 처리된 내피세포를 Flow cytomwtry로 분석하여 항체가 부착된 내피세포의 비율을 알아냄으로써 내피세포의 항원성(antigenic expression)을 조사하였다. 또한 보존처리된 동종동맥판에 의한 생체내에서의 면역반응을 평가하기 위하여 위에서와 같은 방법으로 보존처리전(No treat), 멸균처리 후 2일 보존후(2 day), 7일 보존후(7 day), 14일 보존 후(14 day), 냉동보존(cryo)된 동종동맥판을 Mouse에 이식한 후 일정기간(1, 2, 3, 4, 6, 8주)이 경과된 시점에서 혈중의 CD4$^{+}$, CD8$^{+}$ T cell분포를 측정하였다. 이를 위하여 Mouse의 미정맥에서 채취한 혈액에 monoclonal antibody를 처리한 뒤 flow cytometry를 이용하여 lymphocyte중의 CD4$^{+}$, CD8$^{+}$ T cell 비율을 측정하였다. 내피세포의 MHC Class I 표현정도는 No treat에서 23.95%였고, sterile에서 48.08%로 증가한 뒤 14day 까지 36.02%로, cryo에서도 35.53% 로 증가되어 있었다(p=0.0183). MHC Class II 표현정도는 No treat에서 9.72%, sterile에서 10.13%이였고 14day 에서 10.27%, cryo 에서 13.39% 였다(P=0.1599). ICAM-1 표현정도는 No treat에서 15.02%, sterile에서 19.85%였고, 14day에서 35.33%, cryo에서 34.67% 로 증가하였다(P=0.001). 정상 Mouse에서 CD4$^{+}$, CD8$^{+}$ T-cell분포는 각각 42.13%, 25.57% 였고 CD4$^{+}$/CD8$^{+}$ ratio는 1.64였다. 동종동맥을 이식받은 Mouse의 정맥혈중 CD4$^{+}$ T-cell분포는 No treat군에서 1주에서 8주사이에 49.23% 에서 36.8%사이로 변화를 보이지 않았고(p=0.955), 2 day군에서는 30.36%로 감소하였고(p=0.0001), 7day군에서는 32.8%로 감소하였고(p=0.008), 14 day 군은 26.92%로 감소(p=0.0001), cryo군은 29.56%로 감소하였다(p=0.0018). CD8$^{+}$T-cell은 모든 군에서 1주에서 8주 사이에 42.32%에서 58.92%사이로 증가하였다(p=0.0001~0.0002). CD4$^{+}$/CD8$^{+}$ ratio는 모든 군에서 1주에 1.22 에서 2.28 사이에 있었으나 8주후에는 모든 군에서 0.47에서 0.95 사이로 감소하였다(p=0.0001). 즉, 보존처리된 동종동맥판의 내피세포는 보존처리과정의 초기에는 MHC class I과 II항원효과를 동시에 보이고, 보존기간이 길어지면서 MHC class II항원효과는 변함이 없으나 MHC class I 항원효과는 증가함을 알 수 있다. 또한 CD4$^{+}$ T-cell은 보존처리 기간 중 소폭의 변환를 보임에 반하여 CD8$^{+}$ T-cell은 보존처리된 기간에 관계없이 이식된 후 8주간에 걸쳐 지속적으로 증가함을 알 수 있다. 4$^{\circ}C$에 냉장보존한 군과 냉동보존한 군간에는 차이가 없었다. 이와같은 결과를 볼 때 동종동맥판을 체내에 이식할 경우 내피세포에 의한 MHC class I 항원효과가 지속적으로 유지되고 있음을 추측할 수 있다.

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항암(抗癌) 및 면역효과(免疫效果)에 복분자약침(覆盆子藥鍼)이 미치는 영향(影響) (Study on the Anti-cancer, Anti-metastasis and Immune response improvement Effects of Aqua-acupuncture with Rubi Fructus infusion solution)

  • 이선희;이병렬
    • Journal of Acupuncture Research
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    • 제17권1호
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    • pp.189-219
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    • 2000
  • To study the effects of anti-cancer, anti-metastasis and immune response improvement effects of aqua-acupuncture with Rubi Fructus infusion solution, we used Rubi Fructus infusion solution(taken by water-alcohol method) put into Chung-wan (CV12) and Chok-Samni(ST36) of BALB/c or C57BL/6 which are corresponding to humanbody. We observed the cytotoxicity, the effect on the expression of MMP-9 gene, the ability to control cancer cell proliferation, change of body weight, surviving number, median surviving time, increase of life span, changes in amount of leukocyte, erythrocyte, platelet, total protein, creatinine, glucose and LDH, weight of spleen, number of pulmonary colony, histological analysis on tissue metastasis of lung and liver, splenic cell proliferation, the expression of cytokine gene, the number of $CD4^+$, $CD8^+$, $CD19^+$ and NK cell, and concluded like this. The results were obtained as follows : 1. Effects of Anti-cancer 1) The cytotoxicity about B16-F10 cell line of $2^0$, $2^{-1}$, $2^{-2}$, $2^{-3}$, $2^{-5}$, $2^{-6}$, $2^{-7}$, $2^{-8}$ diluent groups in Rubi Fructus infusion solution treatment was inhibited significantly, compared with control group. 2) The cytotoxicity about HT1080 cell line of $2^0{\sim}2^{-8}$ diluent groups in Rubi Fructus infusion solution treatment was inhibited significantly, compared with control group. 3) The effect on expression of MMP-9 gene was inhibited significantly in all the sample groups, compared with control group. 4) The effect on the control-ability on the cancer cell proliferation showed cytotoxicity significantly in $2^0$, $2^{-1}$, $2^{-2}$, $2^{-3}$, $2^{-4}$, $2^{-5}$, $2^{-6}$, $2^{-7}$, diluent groups. 2. Effects of Anti-metastasis 1) S-180 cancer cell line transplants in BALB/c mice were inhibited significantly in weight increase in all the sample groups, compared with control group. The surviving number increased in almost sample groups, except one group put into Chok-Samni(ST36) with 20% Rubi Fructus infusion solution treatment group that showed same number of the control group. 2) S-180 cancer cell line transplants in BALB/c mice showed high MST significantly in almost sample groups, compared with control group. But one group put into Chok-Samni(ST36) with 20% Rubi Fructus infusion solution showed low MST than control group. 3) The group injected in vein with B16-F10 cancer cell line in C57BL/6 mice showed increased ILS than control group significantly in anti-metastasis test. 3. Effects of Immune response improvement 1) The group injected in vein with B16-F10 cancer cell line in C57BL/6 mice were increased significantly in the number of leukocyte and glucose, and decreased significantly in the amount of platelet and LDH, compared with control group. However, there's no significant increase or decrease in number of erythrocyte, total protein and creatinine. 2) We couldn't find any significant relation in spleen weight of the sample group. 3) In pulmonary colony, sample group was decreased significantly, compared with control group. 4) Histological analysis of sample group inhivited compared with that of control group in both of lung and liver. 5) In immune system, all the sample groups showed having more relevancy to the effect on splenic cell proliferation than normal group. 6) Cytokine gene increased in almost sample groups, except one group treated with $50{\mu}g/m{\ell}$ Rubi Fructus infusion solution on IL-12. 7) In flow cytometry there's no significant relation in number of $CD8^+$ cell, however, the number of $CD4^+$, $CD19^+$ cell and NK cell in sample group had more relation than in control group. Above the results showed that aqua-acupuncture of Rubi Fructus solution has effects of anti-cancer, and-metastasis and immune response improvement.

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육종용약침의 항암작용(抗癌作用) 및 면역효과(免疫效果)에 대(對)한 실험적(實驗的) 연구(硏究) (Study on the Anti-cancer, Anti-metastasis and Immune response improvement of Aqua-acupuncture with Cistanches Herba infusion solution)

  • 이은용;이병렬
    • Journal of Acupuncture Research
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    • 제17권1호
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    • pp.251-286
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    • 2000
  • To study the effects of anti-cancer, anti-metastasis and immune response improvement of aqua-acupuncture with Cistanches Herba infusion solution, we used Cistanches Herba infusion solution(taken by water-alcohol method) put into Chung-wan(CV12) and Chok-Samni(S36) of BALB/c or C57BL/6 which are corresponding to human body. We observed the cytotoxicity, the effect on the expression of MMP-9 gene, the ability to control cancer cell proliferation, change of body weight, surviving number, MST, ILS, changes in amount of WBC, RBC, PLT, total protein, creatinine, glucose and LDH, weight of spleen, number of pulmonary colony, histological analysis on tissue metastasis of lung and liver, splenic cell proliferation, the expression of cytokine gene, the number of $CD4^+$, $CD8^+$, $CD19^+$ and NK cell, and concluded like this. The results were obtained as follows : 1. The cytotoxicity about B16-F10 cell line of $2^0$, $2^{-1}$, $2^{-2}$, $2^{-5}$ diluent groups in Cistanches Herba infusion solution treatment was inhibited significantly, compared with control group. 2. The cytotoxicity about HT1080 cell line of $2^0$, $2^{-1}$, $2^{-2}$, $2^{-3}$, $2^{-5}$, $2^{-8}$ diluent groups in Cistanches Herba infusion solution treatment was inhibited significantly, compared with control group. 3. The effect on expression of MMP-9 gene was decreased in all the sample groups, compared with control group. 4. The effect on the control-ability on the cancer cell proliferation showed cytotooicity significantly in $2^0$, $2^{-1}$, $2^{-2}$, $2^{-3}$, $2^{-4}$, $2^{-5}$ diluent groups. 5. S-180 cancer cell line transplants in BALB/c mice were inhibited significantly in weight increase in all the sample groups, compared with control group. The surviving number increased in almost sample groups, except one group put into Chok-Samni(S36) with 20% Cistanches Herba infusion solution treatment group that showed same number of the control group. 6. S-180 cancer cell line transplants in BALB/c mice showed high MST and ILS significantly in almost sample groups, compared with control group. But one group put into Chok-Samni(S36) with 20% Cistanches Herba infusion solution treatment group showed low MST and ILS than control group. 7. The sample group injected in vein with B16-F10 cancer cell line in C57BL/6 mice showed increased ILS compared with control group significantly in anti-metastasis test. 8. The sample group injected in vein with B16-F10 cancer cell line in C57BL/6 mice were increased significantly in the number of WBC and glucose, and decreased significantly in the amount of LDH, compared with control group. However, there's no significant increase or decrease in number of RBC, PLT, total protein and creatinine. 9. We couldn't find any significant relation in spleen weight of the sample group. 10. In pulmonary colony, sample group was decreased significantly, compared with control group. 11. Histological analysis of sample group inhivited compared with that of control group in both of lung and liver. 12. In immune system, all the sample groups showed having more relevancy to the effect on splenic cell proliferation than normal group. 13. The effect on cytokine gene expression of all the sample groups were increased than control group. 14. In flow cytometry there's no significant relation in number of $CD8^+$, $CD19^+$ cell, however, the number of $CD4^+$ cell and NK cell in sample groups were increased than in control group. Above the results showed that aqua-acupuncture of Cistanches Herba infusion solution has effects of anti-cancer, anti-metastasis and immune response improvement.

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