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Updated: Jun 23, 2026

Evaluation of the Interplay Between the Complement Protein C1q and Hyaluronic Acid in Promoting Cell Adhesion
Published on: June 15, 2019
[Structure and function of complement protein C1q and its role in the development of autoimmune diseases]
Katarzyna Smykał-Jankowiak1, Zofia I Niemir
1Pracownia Nefrologii Molekularnej, Katedra i Klinika Nefrologii, Transplantologii i Chorób Wewnetrznych Uniwersytetu Medycznego im. K. Marcinkowskiego w Poznaniu, 60-355 Poznań.
Insights
Complement component C1q is crucial for immune responses and clearing cellular debris. Mutations in the C1q gene are linked to infections and lupus, with anti-C1q antibodies aiding diagnosis.
Area of Science:
- Immunology
- Molecular Biology
Context:
- The complement system is vital for innate and adaptive immunity, involving over 30 serum peptides.
- C1q initiates the classical complement pathway, binding immune complexes via its C-terminal heads.
Purpose:
- To elucidate the multifaceted roles of C1q beyond complement activation.
- To review the genetic basis and clinical implications of C1q deficiency and anti-C1q antibodies.
Summary:
- C1q, a key component of the classical complement pathway, interacts with diverse ligands including aggregated immunoglobulins, viruses, and apoptotic cells.
- Beyond complement activation, C1q facilitates immune complex clearance, removes necrotic cells, and modulates lymphocyte function.
- Complete C1q deficiency, caused by rare gene mutations, predisposes individuals to recurrent bacterial infections and systemic lupus erythematosus (SLE).
Impact:
- Understanding C1q's functions is critical for comprehending immune system regulation and host defense.
- Anti-C1q antibodies are significant biomarkers for diagnosing and monitoring lupus nephritis activity.
- Research into C1q and its associated disorders may lead to novel therapeutic strategies for autoimmune diseases and infections.
Abstract:
Complement plays an important role in the immune system. Three different pathways of complement activation are known: the classical, alternative, and lectin dependent. They involve more than 30 serum peptides. C1q is the fi rst subcomponent of the classical pathway of complement activation.It is composed of three types of chains, A, B, and C, which form a molecule containing 18 peptides. Each of the chains has a short amino-terminal region followed by a collagen-like region(playing a role in the activation of C1r2C1s2) and a carboxy-terminal head, which binds to immune complexes. Recent studies have shown a great number of ligands for C1q, including aggregated IgG, IgM, human T-cell lymphotropic virus-I (HTLV-I), gp21 peptide, human immunodeficiency virus-1 (HIV-1) gp21 peptide, beta-amyloid, fragments of bacterial walls, apoptotic cells, and many others. However, the role of C1q is not only associated with complement activation.It also helps in the removal of immune complexes and necrotic cells, stimulates the production of some cytokines, and modulates the function of lymphocytes. Complete C1q deficiency is a rare genetic disorder. The C1q gene is located on the short arm of chromosome 1. So far, only a few mutations in C1q gene have been reported. The presence of these mutations is strongly associated with recurrent bacterial infections and the development of systemic lupus erythematosus(SLE). Recent clinical studies point to the significance of anti-C1q antibodies in the diagnosis and assessment of lupus nephritis activity.
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