Human cerebrospinal fluid contains diverse lipoprotein subspecies enriched in proteins implicated in central nervous system health

Author:

Merrill Nathaniel J.1ORCID,Davidson W. Sean2ORCID,He Yi3ORCID,Díaz Ludovico Ivo1ORCID,Sarkar Snigdha1ORCID,Berger Madelyn R.1ORCID,McDermott Jason E.14ORCID,Van Eldik Linda J.5ORCID,Wilcock Donna M.5ORCID,Monroe Matthew E.1ORCID,Kyle Jennifer E.1,Bruce Kimberley D.6,Heinecke Jay W.3,Vaisar Tomas3ORCID,Raber Jacob78,Quinn Joseph F.79ORCID,Melchior John T.127ORCID

Affiliation:

1. Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99354, USA.

2. Center for Lipid and Arteriosclerosis Science, Department of Pathology and Laboratory Medicine, University of Cincinnati, Cincinnati, OH 45237, USA.

3. Department of Medicine, University of Washington School of Medicine, Seattle, WA 98109, USA.

4. Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, OR 97239, USA.

5. Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY 40504, USA.

6. Division of Endocrinology, Metabolism and Diabetes, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.

7. Department of Neurology, Oregon Health and Science University, Portland, OR 97239, USA.

8. Division of Neuroscience, Department of Behavioral Neuroscience and Radiation Medicine, ONPRC, Oregon Health and Science University, Portland, OR 97239, USA.

9. Department of Neurology and Parkinson’s Disease Research Education and Clinical Care Center (PADRECC), VA Portland Healthcare System, Portland OR 97239, USA.

Abstract

Lipoproteins in cerebrospinal fluid (CSF) of the central nervous system (CNS) resemble plasma high-density lipoproteins (HDLs), which are a compositionally and structurally diverse spectrum of nanoparticles with pleiotropic functionality. Whether CSF lipoproteins (CSF-Lps) exhibit similar heterogeneity is poorly understood because they are present at 100-fold lower concentrations than plasma HDL. To investigate the diversity of CSF-Lps, we developed a sensitive fluorescent technology to characterize lipoprotein subspecies in small volumes of human CSF. We identified 10 distinctly sized populations of CSF-Lps, most of which were larger than plasma HDL. Mass spectrometric analysis identified 303 proteins across the populations, over half of which have not been reported in plasma HDL. Computational analysis revealed that CSF-Lps are enriched in proteins important for wound healing, inflammation, immune response, and both neuron generation and development. Network analysis indicated that different subpopulations of CSF-Lps contain unique combinations of these proteins. Our study demonstrates that CSF-Lp subspecies likely exist that contain compositional signatures related to CNS health.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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