IVC / TM / GBA2, Acid ceramidase inhibitor Yuta exec summary, Acid ceramidase / Farber lipogranulomatosis genetics

GBA2

content
locationAt the plasma membrane, cytoplasmic face of the ER and Golgi (ie Non-lysosomal)
expressiontestis, liver, and brain, in particular in Purkinje cells
mutations in the GBA2 genethe ataxia-spasticity spectrum
functioncleaves the same natural and artificial substrates as GBA
Inhibition byN-butyldeoxygalactonojirimycin (NB-DGJ), inhibits GBA2 but does not affect GBA
CBE inhibits both.
NoteGBA2 activity is regulated by GBA activity, but not vice versa [59].

Model system

SourceModelFindings
Cayman
(Marques, 2016 #603)COS-7 cell (African green monkey kidney cell), transfected with GBAInhibition of GBA with CBE prevented formation of GlcCer + Chol → GlcChol (Fig. 3A).
Alfonso, Pilar et alMiglustat (NB-DNJ) works as a chaperone for mutated acid β-glucosidase in cells transfected with several Gaucher disease mutationsBlood Cells, Molecules, and Diseases 35.2 (2005) 268-276
No info on CBE
(Ridley, 2013 #600)COS-7 cell (not a transfected cell)Fig 4A, CBE (2.5 mM) completely blocked β-glucosidase activity (ie blocked GBA & GBA2)
(Liu, 2015 #601)Cynomolgus monkeysAging: ↑ aSyn oligomer & ↑ p-aSyn, ↓ PPA2A (protein phosphatase 2A), ↓ GBA protein, ↓ GBA activity
Primary cultures of rat cortical neurons & MES 23.5 dopaminergic cellsCBE → oligomeric a-syn increased

Acid Ceramidase inhibitor — Executive summary (Yuta) (PFR-4153-100)

LGE (AQB1 202303)PE (FY21 Q4)CN
In vitroCell free enz assay (IC50 < 100 nM)
Cell-based: GBA KO cell (HAP1), ↓ (어느만큼?) GlcSph (IC50 < 100 nM)
Effect on GalSph reduction will be confirmed in cellular assay (fibroblast or mouse primary neuron) before in vivo PK/PD study.
GD iPS DA neuron (L444P/L444P)
POC for GD: ↓ (어느만큼? Monthly report 보자) GlcSph
PD iPS neuron
POC for PD: a-syn reduction. 202103 까지 낮췄음, → plan: selective MOA, & Venglu 검사
In vivoGalSph reduction in C57/BL miceGba D409V mice
POC for GD: GlcSph reduction in brain
aSyn PFF mice or SNCA-A53T mice (Under discussion)
POC for PD: a-syn reduction in brain

https://mytakeda.sharepoint.com/sites/InterACT-RAD-Pipeline/NS%20DU%20ACi/Site%20Pages/Team%20Document%20Management.aspx

HAP1 cells are a near-haploid cell line derived from the KBM-7 cell line. KBM-7 was found in a patient with chronic myeloid leukemia (CML).

Questions / Research hypothesis

The level of psychosine in GD or GBA-PD?

Lysosome / Research hypothesis?

  • Lysosomal dysfunction → ↑ aSyn degradation, then why aSyn?
  • aSyn 증가가 positive control 식으로 필요
  • Lysosomal dysfunction → global protein degradation → neurodegeneration
  • Global proteolysis 감소가 positive control 식으로 필요
  • BM discovery effort
  • 적어도 aSyn 보이는 model 에서 해야 안하나
  • Protein degradation 필요?
  • P62 로 되겠나?
  • LAMP, p62 등 이미 봤다는 것은 어디?
  • iPS에서 comprehensive하게 왔나?
  • Work with phReT?
  • Human postmortem brain에서 볼 생각 있나?
  • Mouse model
  • GD CSF (Tottori)
  • Interpretation is challenging: eg. trapping of ATG proteins in autophagosomes, the dynamics of ATG proteins, actual change in the autophagy process, reduced autophagosome formation but also to increased autophagosome degradation

Acid ceramidase

fieldcontent
gene nameN-acylsphingosine amidohydrolase 1 (ASAH1)
protein nameacid ceramidase (AC, aCDase)
tissue distributionubiquitous
subcellular localizationlysosome
functionHydrolysis of amide on ceramide side-chain by AC generates lyso-sphingolipids in lysosome

Substrates of AC (ie if AC ↑ → ↓ all below)

  • ceramide
    • NOTE!) 우리 약으로 AC막으면, ceramide가 늘면 inflammation, insulin signaling inhibition, and Bcl-2 family protein-mediated apoptosis
  • glucosylceramide (GlcCer)
  • galactosylceramide (GalCer)

Product of AC (ie AC ↑ → ↑ all below)

  • sphingoshine (=Sph) (& lipids)
  • GlcSph
  • galactosylSph (= psychosine, = globoid cell leukodystrophy)
    • psychosine induces aggregation of a-syn in NSC34 motor-neuron cells (Abdelkarim et al., 2018, PMID 30127535)

Pathway notes

Ceramide가 다시 lysosome 밖으로 나가서 → GCS에 의해 GlcCer (UGCG 일걸) 가 됨.

GlcCer는 ① lysosome안에서 GBA에 의해 Ceramide만들기도 하지만, ② (Acid ceramidase=ASAH1, 에 의해) GlcSph로 되기도 함. → 이 GlcSph 가 (acid ceramidase 에 의해) Sphingosine 되는 것임 → 이후 다른 sphingolipid 로 진행될걸 (glucosylceramide hydrolysis accounts for 50-90% of sphingolipid production.)

Lysosome cartoons

Healthy people vs Patients with GBA mutations (Golgi → Lysosome):

  • Healthy: Cer → GlcCer ----→ GlcCer → Cer (GCS / A C / GlcSph → Sph)
  • Patients with GBA mutations: Cer → GlcCer ----→ GlcCer → Cer (GBA↓; GlcSph → Sph)

Specific lysosomes:

  • Lysosome of Gaucher disease: GlcCer → AC → GlcSph (GBA ↓)
  • Lysosome of Krabbe disease: GlcCer → AC → GalSph (GALC ↓ → Sph)

Genetics ASAH1 / Farber lipogranulomatosis

Variants in the ASAH1 gene lead to severe reduction in acid ceramidase, typically to below 10 percent of normal. As a result, the enzyme cannot break down ceramides properly and they build up in the lysosomes of various cells, including in the lung, liver, colon, muscles used for movement (skeletal muscles), cartilage, and bone. The buildup of ceramides along with the reduction of its fatty breakdown products in cells likely causes the signs and symptoms of Farber lipogranulomatosis. It is unclear whether the level of acid ceramidase activity is related to the severity of the disorder. → Three classic signs occur in Farber lipogranulomatosis: a hoarse voice or a weak cry, small lumps of fat under the skin and in other tissues (lipogranulomas), and swollen and painful joints. Signs and symptoms typically first develop in infancy.

[Robak 2017] In these gene-based analyses, besides the expected result for GBA (P = 0.0001) and confirmation of SMPD1 (P = 0.029), we discover evidence of novel aggregate associations for variants in CTSD (P = 0.002), SLC17A5 (P = 0.005), and ASAH1 (P = 0.031).

Uncertain Spans

locationtranscriptionuncertainty
Healthy people / GBA-mutation cartoonsthe diagrams are approximated as text-only abstractionsthe source includes paired cell-cartoon diagrams; only the text labels are transcribed.