Secretomics reveals gelatinase substrates at the blood-brain barrier that are implicated in astroglial barrier function

Author:

Burmeister Miriam12ORCID,Fraunenstein Annika3,Kahms Martin24,Arends Laura12ORCID,Gerwien Hanna12,Deshpande Tushar12ORCID,Kuhlmann Tanja25,Gross Catharina C.26ORCID,Naik Venu N.26ORCID,Wiendl Heinz267ORCID,Klingauf Juergen24,Meissner Felix38ORCID,Sorokin Lydia12ORCID

Affiliation:

1. Institute of Physiological Chemistry and Pathobiochemistry, University of Muenster, Münster, Germany.

2. Cells-in-Motion Interfaculty Centre (CIMIC), University of Muenster, Münster, Germany.

3. Max-Planck Institute for Biochemistry, Martinsried, Germany.

4. Institute of Medical Physics and Biophysics, University of Muenster, Münster, Germany.

5. Institute of Neuropathology, University Hospital Muenster, Münster, Germany.

6. Neurology Department., University Clinic, University of Muenster, Münster, Germany.

7. Brain and Mind Center,, Sydney, New South Wales, Australia.

8. Institute of Innate Immunity, Department of Systems Immunology and Proteomics, Medical Faculty, University of Bonn, Bonn, Germany.

Abstract

The gelatinases, matrix metalloproteinase 2 (MMP-2) and MMP-9, are key for leukocyte penetration of the brain parenchymal border in neuroinflammation and the functional integrity of this barrier; however, it is unclear which MMP substrates are involved. Using a tailored, sensitive, label-free mass spectrometry–based secretome approach, not previously applied to nonimmune cells, we identified 119 MMP-9 and 21 MMP-2 potential substrates at the cell surface of primary astrocytes, including known substrates (β-dystroglycan) and a broad spectrum of previously unknown MMP-dependent events involved in cell-cell and cell-matrix interactions. Using neuroinflammation as a model of assessing compromised astroglial barrier function, a selection of the potential MMP substrates were confirmed in vivo and verified in human samples, including vascular cell adhesion molecule–1 and neuronal cell adhesion molecule. We provide a unique resource of potential MMP-2/MMP-9 substrates specific for the astroglia barrier. Our data support a role for the gelatinases in the formation and maintenance of this barrier but also in astrocyte-neuron interactions.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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