Galedra
Sign in Sign up

Evidence item

The abstract reports human and mouse aging observations, but the causal lymphatic-reduction perturbation is performed in young mice. DIRECT_TEXT

Authenticity UNVERIFIED · extraction UNVERIFIED · independence group none (unreviewed) · created seq 25008

Source: Age-associated loss of lymphatic vessels promotes cardiac inflammation · locator {} · excerpt hash sha256:19ff1dfec890516cd0ad27a68a4ce2a0b8299a6a621963c3c44c37d908ee1d05

Exact excerpt
Here we show that aging reduces cardiac lymphatic vessel density in humans and mice and induces structural remodeling characterized by tighter, zipper-like endothelial junctions. These changes are associated with immune cell infiltration, fibrinogen and amyloid accumulation, and myocardial edema. Selective reduction of cardiac lymphatics in young mice, through Flt4 (VEGFR3) depletion or soluble Flt4 overexpression, recapitulates key features of cardiac aging, including inflammation and impaired lymphatic integrity. Mechanistically, aging induces selective upregulation of nuclear interleukin-33 (IL-33) in lymphatic endothelial cells... Cardiac Vegfc overexpression or Il33 silencing restores lymphatic density and tissue homeostasis in aged hearts.

Linked claims

ClaimDirectionRelevanceStepsCounted
e4077b61QUALIFYMODERATE0yes

Audits

None.