Sofia Spataro

Dr. Sofia Spataro

orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 July 2019 in Nature Medicine
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Journal Article
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BGBence György
Bence György
CNCarl Nist-Lund
Carl Nist-Lund
BPBifeng Pan
Bifeng Pan
YAYukako Asai
Yukako Asai
KKK. Domenica Karavitaki
K. Domenica Karavitaki
DCDavid P. Corey
David P. Corey

5 September 2022 in The FEBS Journal
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Journal Article
Open access
SSSofia Spataro
Sofia Spataro
CGConcetta Guerra
Concetta Guerra
ACAndrea Cavalli
Andrea Cavalli
JSJacopo Sgrignani
Jacopo Sgrignani
JSJonathan P. Sleeman
Jonathan P. Sleeman
MPMarco Prunotto
Marco Prunotto
CEMIP (cell migration‐inducing protein), also known as KIAA1199 or HYBID, is a protein involved in the depolymerisation of hyaluronic acid (HA), a major glycosaminoglycan component of the extracellular matrix. CEMIP was originally described in patients affected by nonsyndromic hearing loss and has subsequently been shown to play a key role in tumour initiation and progression, as well as arthritis, atherosclerosis and idiopathic pulmonary fibrosis. Despite the vast literature associating CEMIP with these diseases, its biology remains elusive. The present review article summarises all the major scientific evidence regarding its structure, function, role and expression, and attempts to cast light on a protein that modulates EMT, fibrosis and tissue inflammation, an unmet key aspect in several inflammatory disease conditions.

9 April 2022 in Matrix Biology
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Journal Article
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ASAnja Schmaus
Anja Schmaus
MRMelanie Rothley
Melanie Rothley
CSCaroline Schreiber
Caroline Schreiber
SMStephanie Möller
Stephanie Möller
SRSven Roßwag
Sven Roßwag
JSJonathan Sleeman
Jonathan Sleeman

11 January 2025 in Cells
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Journal Article
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ASAnja Schmaus
Anja Schmaus
SSSofia Spataro
Sofia Spataro
PSPaul Sallmann
Paul Sallmann
SMStephanie Möller
Stephanie Möller
LSLeonardo Scapozza
Leonardo Scapozza
JSJonathan P. Sleeman
Jonathan P. Sleeman
Hyaluronan (HA) levels are dynamically regulated homeostatically through biosynthesis and degradation. HA homeostasis is often perturbed under disease conditions. HA degradation products are thought to contribute to disease pathology. The hyaluronidase CEMIP requires the presence of living cells for its HA depolymerizing activity. CEMIP is overexpressed in a variety of pathological conditions, and the inhibition of its hyaluronidase activity therefore has therapeutic potential. To identify novel inhibitors of the CEMIP hyaluronidase activity, we established here a cell-compatible, medium-throughput assay for CEMIP-dependent HA depolymerization. The assay employs ultrafiltration plates to separate low- from high-molecular-weight HA, followed by quantification of HA fragments using an HA ELISA-like assay. Using this assay, we tested a range of compounds that have been reported to inhibit other hyaluronidases. Thereby, we identified several sulfated hydrocarbon polymers that inhibit CEMIP more potently than other hyaluronidases. One of these is heparin, a sulfated glycosaminoglycan produced by mast cells that constitutes the first described physiological CEMIP inhibitor. The most potent inhibitor (IC50 of 1.8 nM) is dextran sulfate, a synthetic sulfated polysaccharide. Heparin and dextran sulfate are used in numerous established and experimental biomedical applications. Their ability to inhibit CEMIP needs to be taken into account in these contexts.