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関連する概念動画

Cell-mediated Immune Responses01:40

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Differentiation of Common Myeloid Progenitor Cells01:15

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Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...
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Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

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All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
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Immunoglobulin-like Cell Adhesion Molecules01:31

Immunoglobulin-like Cell Adhesion Molecules

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Immunoglobulin-like cell adhesion molecules or Ig-CAMs are a versatile group of cell surface glycoproteins belonging to the immunoglobulin protein superfamily. Ig-CAMs possess the characteristic immunoglobulin protein domains and other domains such as the fibronectin type III domain. The Ig domains are glycosylated to varying degrees in different Ig-CAMs.
Ig-CAMs exhibit either homophilic binding (to other Ig-CAMs) or heterophilic binding (to other ligands such as integrins). While most Ig-CAMs...
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Cytotoxic T Cells-mediated Immune Response01:27

Cytotoxic T Cells-mediated Immune Response

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Cytotoxic T cells are a vital component of the immune system. They have the remarkable ability to identify and target antigens on infected or abnormal cells. These antigens often originate from intracellular pathogens such as viruses or abnormal proteins cancer cells produce.
Immunological surveillance is the ability of immune cells to monitor and eliminate infected cells with intracellular pathogens, neoplastically transformed cells, and cells with non-self antigens. Cytotoxic T cells and NK...
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Complement System01:27

Complement System

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The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a...
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Measuring the 50% Haemolytic Complement CH50 Activity of Serum
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確立された細胞系によって分泌される補完体のC3成分.

D R Senger, R O Hynes

    Cell
    |October 1, 1978
    PubMed
    まとめ

    ハムスター細胞はコンプリメントC3を分泌し,これは古典的および代替的経路で活性化されます. この研究は,C3が非活性前駆体 (proC3) として合成され,活性化するために分裂することを明らかにしています.

    科学分野:

    • 免疫学 免疫学とは
    • 細胞生物学 細胞生物学
    • バイオケミストリー バイオケミストリー

    背景:

    • ハムスター細胞系NIL8は,コンプリメントコンポーネント3 (C3),コラーゲン,フィブロネクチンを分泌する.
    • 分泌されるC3は,アルファ (130 kDa) とベータ (65 kDa) ポリペプチドの二硫化物結合複合体として存在します.

    研究 の 目的:

    • NIL8細胞によって分泌されるC3の合成,活性化,補完経路の関与を調査する.
    • C3の前駆体形態とその活性成分への変換を特徴付ける.

    主な方法:

    • NIL8ハムスター細胞を培養し,分泌されるタンパク質を分析する.
    • ジモザンと抗体でコーティングされた赤血球を用いてC3活性化の研究.
    • C3 (proC3) の前駆体形態とその裂解産物の特徴について.

    主要な成果:

    • NIL8細胞はC3を分泌し,C3bに分割され,C3不活性化剤によってさらに処理されます.
    • C3bへのC3活性化は,古典的および代替的な補足経路の両方によって媒介されます.
    • C3は不活性な185 kDa前駆体 (proC3) として合成され,活性なC3を生成するために分裂されます.

    さらに関連する動画

    Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
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    Measuring Erythrocyte Complement Receptor 1 Using Flow Cytometry
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    Last Updated: Apr 30, 2026

    Measuring the 50% Haemolytic Complement CH50 Activity of Serum
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    Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
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    Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion

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    Measuring Erythrocyte Complement Receptor 1 Using Flow Cytometry
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    Measuring Erythrocyte Complement Receptor 1 Using Flow Cytometry

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    結論:

    • NIL8細胞培養システムは,補完体C3の合成と活性化を研究するためのモデルを提供します.
    • C3の分泌と活性化は,一部の細胞系 (NIL1,BALB/c 3T3) で観察されるが,他では観察されない.
    • この発見は,コンプリメントC3の生物学的処理を,不活性な前駆体から免疫反応に関与する活性成分へと解明しています.