Abstract
Recent rapid progress in key technological advances, including the broader accessibility of single-cell “omic” approaches, have allowed immunologists to gain important novel insights into the contributions of individual immune cells in protective immunity and immunopathologies. These insights also taught us that there is still much to uncover about the (cellular) networks underlying immune responses. For example, in the last decade, studies on a key component of innate immunity, the complement system, have defined intracellularly active complement (the complosome) as a key orchestrator of normal cell physiology. This added an unexpected facet to the biology of complement, which was long considered fully explored. Here, we will summarize succinctly the known activation modes and functions of the complosome and provide a perspective on the origins of intracellular complement. We will also make a case for extending assessments of the complotype, the individual inherited landscape of common variants in complement genes, to the complosome, and for reassessing patients with known serum complement deficiencies for complosome perturbations. Finally, we will discuss where we see current opportunities and hurdles for dissecting the compartmentalization of complement activities toward a better understanding of their contributions to cellular function in health and disease.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 2250042 |
| Zeitschrift | European Journal of Immunology |
| Jahrgang | 53 |
| Ausgabenummer | 12 |
| ISSN | 0014-2980 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 12.2023 |
Fördermittel
The Kemper laboratory is supported by the Division of Intramural Research, National Heart, Lung, and Blood Institute (NHLBI) at the National Institutes of Health (NIH) (project number zia/hl006223 to C.K.).
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
- Zentren: Center for Research on Inflammation of the Skin (CRIS)
DFG-Fachsystematik
- 2.21-05 Immunologie
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