A Cell Biologist’s View on APOL1: What We Know and What We Still Need to AddressOpen Access

Höffken, Verena; Braun, Daniela Anne; Pavenstädt, Hermann; Weide, Thomas

Übersichtsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

APOL1 is the most recent member of the APOL gene family and is expressed exclusively in humans and a few higher primates. More than twenty years ago, it was discovered that APOL1 protects humans from infections by trypanosome subspecies that cause African sleeping sickness. Interestingly, by a co-evolutionary process between parasite and host, two APOL1 variants emerged, which, in addition to their trypanotoxic effects, are simulta- neously associated with a significantly increased risk for various different kidney diseases, which are now summarized as APOL1-mediated kidney diseases (AMKDs). The aim of this review is to highlight and formulate key aspects of APOL1’s cell biologic features, including questions and unaddressed aspects. This perspective may contribute to a deeper understanding of APOL1-associated cytotoxicity as well as AMKDs.

Details zur Publikation

FachzeitschriftCells (Cells)
Jahrgang / Bandnr. / Volume14
Seitenbereich960null
StatusVeröffentlicht
Veröffentlichungsjahr2025 (24.06.2025)
Sprache, in der die Publikation verfasst istEnglisch
DOI10.3390/cells14130960
StichwörterAPOL1; Apolipoprotein L1; APOL1-mediated kidney disease; AMKD; renal risk variants; nephrotoxicity; topology; ion pore

Autor*innen der Universität Münster

Braun, Daniela Anne
Medizinische Klinik D (Med D)
Höffken, Verena
Medizinische Klinik D (Med D)
Pavenstädt, Hermann-Joseph
Medizinische Klinik D (Med D)
Weide, Thomas
Medizinische Klinik D (Med D)