PLIN1 antibodies target Perilipin-1, a lipid droplet-associated protein that modulates adipocyte lipid storage and lipolysis. PLIN1 exists in two isoforms (A and B) and is essential for protecting lipid droplets from hormone-sensitive lipase (HSL)-mediated hydrolysis . Antibodies against PLIN1 are used to:
Visualize lipid droplets in adipocytes via immunofluorescence or immunohistochemistry.
Quantify PLIN1 expression in Western blotting (detects ~62 kDa perilipin A) .
Investigate autoimmune lipodystrophy linked to anti-PLIN1 autoantibodies .
Pathogenic Mechanism: Anti-PLIN1 autoantibodies disrupt lipid droplet stability by blocking PLIN1’s interaction with ABHD5, increasing basal lipolysis and causing adipose tissue loss .
Clinical Data:
In Vitro Evidence: IgG from AGL patients increases lipolysis in 3T3-L1 preadipocytes by 2–3 fold compared to healthy controls .
Animal Models: PLIN1 autoantibodies are detected in Aire−/− mice, a model of autoimmune polyendocrine syndrome .
Epitope Specificity: Most antibodies target the N-terminal region (e.g., PA1-1051: residues 502–517) , while autoantibodies in AGL patients recognize the ABHD5-binding domain (residues 383–405) .
Cross-Reactivity: Commercial antibodies show reactivity across humans, mice, and rats, but vary in specificity for perilipin isoforms .
Diagnostic Biomarker: PLIN1 autoantibodies are a marker for autoimmune lipodystrophy subtypes, aiding differential diagnosis .
Therapeutic Target: Blocking these autoantibodies could mitigate lipodystrophy progression .