4.5 Article

The interaction between progranulin and prosaposin is mediated by granulins and the linker region between saposin B and C

Journal

JOURNAL OF NEUROCHEMISTRY
Volume 143, Issue 2, Pages 236-243

Publisher

WILEY
DOI: 10.1111/jnc.14110

Keywords

frontotemporal lobar degeneration; lysosomal storage diseases; lysosome; neuronal ceroid lipofuscinosis; progranulin; prosaposin

Funding

  1. Association of Frontotemporal Dementia (AFTD)
  2. NINDS [R01NS088448]
  3. Weill Institute
  4. Harry and Samuel Mann Outstanding Graduate Student Award
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS088448, R21NS081357, R01NS095954] Funding Source: NIH RePORTER

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The frontotemporal lobar degeneration (FTLD) protein progranulin (PGRN) is essential for proper lysosomal function. PGRN localizes in the lysosomal compartment within the cell. Prosaposin (PSAP), the precursor of lysosomal saposin activators (saposin A, B, C, D), physically interacts with PGRN. Previously, we have shown that PGRN and PSAP facilitate each other's lysosomal trafficking. Here, we report that the interaction between PSAP and PGRN requires the linker region of saposin B and C (BC linker). PSAP protein with the BC linker mutated, fails to interact with PGRN and deliver PGRN to lysosomes in the biosynthetic and endocytic pathways. On the other hand, PGRN interacts with PSAP through multiple granulin motifs. Granulin D and E bind to PSAP with similar affinity as full-length PGRN.

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