Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis

Research output: Working paperPreprintResearch

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Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis. / Spaas, Jan; Stede, Thibaux Van der; Jager, Sarah de; Berends, Annet van de Waterweg; Tiane, Assia; Baelde, Hans; Baba, Shahid P; Eckhardt, Matthias; Wolfs, Esther; Vanmierlo, Tim; Hellings, Niels; Eijnde, Bert O.; Derave, Wim.

bioRxiv, 2023. p. 1-51.

Research output: Working paperPreprintResearch

Harvard

Spaas, J, Stede, TVD, Jager, SD, Berends, AVDW, Tiane, A, Baelde, H, Baba, SP, Eckhardt, M, Wolfs, E, Vanmierlo, T, Hellings, N, Eijnde, BO & Derave, W 2023 'Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis' bioRxiv, pp. 1-51. https://doi.org/10.1101/2023.03.30.534899

APA

Spaas, J., Stede, T. V. D., Jager, S. D., Berends, A. V. D. W., Tiane, A., Baelde, H., Baba, S. P., Eckhardt, M., Wolfs, E., Vanmierlo, T., Hellings, N., Eijnde, B. O., & Derave, W. (2023). Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis. (pp. 1-51). bioRxiv. https://doi.org/10.1101/2023.03.30.534899

Vancouver

Spaas J, Stede TVD, Jager SD, Berends AVDW, Tiane A, Baelde H et al. Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis. bioRxiv. 2023 Mar 31, p. 1-51. https://doi.org/10.1101/2023.03.30.534899

Author

Spaas, Jan ; Stede, Thibaux Van der ; Jager, Sarah de ; Berends, Annet van de Waterweg ; Tiane, Assia ; Baelde, Hans ; Baba, Shahid P ; Eckhardt, Matthias ; Wolfs, Esther ; Vanmierlo, Tim ; Hellings, Niels ; Eijnde, Bert O. ; Derave, Wim. / Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis. bioRxiv, 2023. pp. 1-51

Bibtex

@techreport{4722836538a44b57ab983d83fa0d31ea,
title = "Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis",
abstract = "Multiple sclerosis (MS) pathology features autoimmune-driven neuroinflammation, demyelination, and failed remyelination. Carnosine is a histidine-containing dipeptide (HCD) with pluripotent homeostatic properties that is able to improve outcomes in an animal MS model (EAE) when suppliedexogenously. To uncover if endogenous carnosine is involved in, and protects against, MS-related neuroinflammation, demyelination or remyelination failure, we here studied the HCD-synthesizing enzyme carnosine synthase (CARNS1) in human MS lesions and two preclinical mouse MS models (EAE, cuprizone). We demonstrate that due to its presence in oligodendrocytes, CARNS1 expression isdiminished in demyelinated MS lesions and mouse models mimicking demyelination/inflammation, but returns upon remyelination. Carns1-KO mice that are devoid of endogenous HCDs display exaggerated neuroinflammation and clinical symptoms during EAE, which could be partially rescued by exogenous carnosine treatment. Worsening of the disease appears to be driven by a central, not peripheral immune-modulatory, mechanism possibly linked to impaired clearance of the reactive carbonyl acrolein in Carns1-KO mice. In contrast, the presence of CARNS1 and endogenous HCDs does not protect against cuprizone-induced demyelination, and is not required for normal oligodendrocyte precursor cell differentiation and (re)myelin to occur. Exogenously administered carnosine is not effective in blunting demyelination or accelerating remyelination. In conclusion, we show that CARNS1 is diminished in demyelinated MS lesions, which may have detrimental effects on disease progression through weakening the endogenous protection against neuroinflammation.",
keywords = "Faculty of Science, Multiple sclerosis, Experimental autoimmune encephalomyelitis, Cuprizone, CARNS1, Histidinecontaining dipeptides, Carnosine",
author = "Jan Spaas and Stede, {Thibaux Van der} and Jager, {Sarah de} and Berends, {Annet van de Waterweg} and Assia Tiane and Hans Baelde and Baba, {Shahid P} and Matthias Eckhardt and Esther Wolfs and Tim Vanmierlo and Niels Hellings and Eijnde, {Bert O.} and Wim Derave",
note = "(Preprint)",
year = "2023",
month = mar,
day = "31",
doi = "10.1101/2023.03.30.534899",
language = "English",
pages = "1--51",
publisher = "bioRxiv",
type = "WorkingPaper",
institution = "bioRxiv",

}

RIS

TY - UNPB

T1 - Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis

AU - Spaas, Jan

AU - Stede, Thibaux Van der

AU - Jager, Sarah de

AU - Berends, Annet van de Waterweg

AU - Tiane, Assia

AU - Baelde, Hans

AU - Baba, Shahid P

AU - Eckhardt, Matthias

AU - Wolfs, Esther

AU - Vanmierlo, Tim

AU - Hellings, Niels

AU - Eijnde, Bert O.

AU - Derave, Wim

N1 - (Preprint)

PY - 2023/3/31

Y1 - 2023/3/31

N2 - Multiple sclerosis (MS) pathology features autoimmune-driven neuroinflammation, demyelination, and failed remyelination. Carnosine is a histidine-containing dipeptide (HCD) with pluripotent homeostatic properties that is able to improve outcomes in an animal MS model (EAE) when suppliedexogenously. To uncover if endogenous carnosine is involved in, and protects against, MS-related neuroinflammation, demyelination or remyelination failure, we here studied the HCD-synthesizing enzyme carnosine synthase (CARNS1) in human MS lesions and two preclinical mouse MS models (EAE, cuprizone). We demonstrate that due to its presence in oligodendrocytes, CARNS1 expression isdiminished in demyelinated MS lesions and mouse models mimicking demyelination/inflammation, but returns upon remyelination. Carns1-KO mice that are devoid of endogenous HCDs display exaggerated neuroinflammation and clinical symptoms during EAE, which could be partially rescued by exogenous carnosine treatment. Worsening of the disease appears to be driven by a central, not peripheral immune-modulatory, mechanism possibly linked to impaired clearance of the reactive carbonyl acrolein in Carns1-KO mice. In contrast, the presence of CARNS1 and endogenous HCDs does not protect against cuprizone-induced demyelination, and is not required for normal oligodendrocyte precursor cell differentiation and (re)myelin to occur. Exogenously administered carnosine is not effective in blunting demyelination or accelerating remyelination. In conclusion, we show that CARNS1 is diminished in demyelinated MS lesions, which may have detrimental effects on disease progression through weakening the endogenous protection against neuroinflammation.

AB - Multiple sclerosis (MS) pathology features autoimmune-driven neuroinflammation, demyelination, and failed remyelination. Carnosine is a histidine-containing dipeptide (HCD) with pluripotent homeostatic properties that is able to improve outcomes in an animal MS model (EAE) when suppliedexogenously. To uncover if endogenous carnosine is involved in, and protects against, MS-related neuroinflammation, demyelination or remyelination failure, we here studied the HCD-synthesizing enzyme carnosine synthase (CARNS1) in human MS lesions and two preclinical mouse MS models (EAE, cuprizone). We demonstrate that due to its presence in oligodendrocytes, CARNS1 expression isdiminished in demyelinated MS lesions and mouse models mimicking demyelination/inflammation, but returns upon remyelination. Carns1-KO mice that are devoid of endogenous HCDs display exaggerated neuroinflammation and clinical symptoms during EAE, which could be partially rescued by exogenous carnosine treatment. Worsening of the disease appears to be driven by a central, not peripheral immune-modulatory, mechanism possibly linked to impaired clearance of the reactive carbonyl acrolein in Carns1-KO mice. In contrast, the presence of CARNS1 and endogenous HCDs does not protect against cuprizone-induced demyelination, and is not required for normal oligodendrocyte precursor cell differentiation and (re)myelin to occur. Exogenously administered carnosine is not effective in blunting demyelination or accelerating remyelination. In conclusion, we show that CARNS1 is diminished in demyelinated MS lesions, which may have detrimental effects on disease progression through weakening the endogenous protection against neuroinflammation.

KW - Faculty of Science

KW - Multiple sclerosis

KW - Experimental autoimmune encephalomyelitis

KW - Cuprizone

KW - CARNS1

KW - Histidinecontaining dipeptides

KW - Carnosine

U2 - 10.1101/2023.03.30.534899

DO - 10.1101/2023.03.30.534899

M3 - Preprint

SP - 1

EP - 51

BT - Carnosine synthase deficiency aggravates neuroinflammation in multiple sclerosis

PB - bioRxiv

ER -

ID: 342494110