Specific Deoxyceramide Species Correlate with Expression of Macular Telangiectasia Type 2 (MacTel2) in a SPTLC2 Carrier HSAN1 Family

Author:

Wilson Lindsey M. Q.1ORCID,Saba Sadaf2,Li Jun3,Prasov Lev145,Miller Jason M. L.45ORCID

Affiliation:

1. Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA

2. Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA

3. Department of Neurology, Wayne State University School of Medicine, Detroit, MI 48201, USA

4. Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, University of Michigan Medical School, Ann Arbor, MI 48105, USA

5. Cellular and Molecular Biology Program, University of Michigan Medical School, Ann Arbor, MI 48109, USA

Abstract

Hereditary sensory and autonomic neuropathy type 1 (HSAN1/HSN1) is a peripheral neuropathy most commonly associated with pathogenic variants in the serine palmitoyltransferase complex (SPTLC1, SPTLC2) genes, which are responsible for sphingolipid biosynthesis. Recent reports have shown that some HSAN1 patients also develop macular telangiectasia type 2 (MacTel2), a retinal neurodegeneration with an enigmatic pathogenesis and complex heritability. Here, we report a novel association of a SPTLC2 c.529A>G p.(Asn177Asp) variant with MacTel2 in a single member of a family that otherwise has multiple members afflicted with HSAN1. We provide correlative data to suggest that the variable penetrance of the HSAN1/MacTel2-overlap phenotype in the proband may be explained by levels of certain deoxyceramide species, which are aberrant intermediates of sphingolipid metabolism. We provide detailed retinal imaging of the proband and his HSAN1+/MacTel2- brothers and suggest mechanisms by which deoxyceramide levels may induce retinal degeneration. This is the first report of HSAN1 vs. HSAN1/MacTel2 overlap patients to comprehensively profile sphingolipid intermediates. The biochemical data here may help shed light on the pathoetiology and molecular mechanisms of MacTel2.

Funder

NEI

NIH

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. (1-Deoxy)ceramides in bilayers containing sphingomyelin and cholesterol;Colloids and Surfaces B: Biointerfaces;2024-11

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