Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity

Lamanna WC, Baldwin RJ, Padva M, Kalus I, ten Dam G, van Kuppevelt TH, Gallagher JT, von Figura K, Dierks T, Merry CLR (2006)
BIOCHEMICAL JOURNAL 400(1): 63-73.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Lamanna, William C.; Baldwin, Rebecca J.; Padva, Michael; Kalus, InaUniBi; ten Dam, Gerdy; van Kuppevelt, Toin H.; Gallagher, John T.; von Figura, Kurt; Dierks, ThomasUniBi; Merry, Catherine L. R.
Abstract / Bemerkung
HS (heparan sulfate) is essential for normal embryonic development. This requirement is due to the obligatory role for HS in the signalling pathways of many growth factors and morphogens that bind to sulfated domains in the HS polymer chain. The sulfation patterning of HS is determined by a complex interplay of Golgi-located N- and O-sulfotransferases which sulfate the heparan precursor and cell surface endosulfatases that selectively remove 6-O-sulfates from mature HS chains. In the present study we generated single or double knock-out mice for the two murine endosulfatases mSulf1 and mSulf2. Detailed structural analysis of HS from mSulf1(-/-) fibroblasts showed a striking increase in 6-O-sulfation. which was not seen in mSulf2(-/-) HS. Intriguingly, the level of 6-O-suffation in the double mSulf1(-/-)/2(-/-) HS was significantly higher than that observed in the mSulf1(-/-) counterpart. These data imply that mSulf1 and mSulf2 are functionally co-operative. Unlike their avian orthologues, mammalian Sulf activities are not restricted to the highly sulfated S-domains of HS. Mitogenesis assays with FGF2 (fibroblast growth factor 2) revealed that Sulf activity decreases the activating potential of newly-synthesized HS, suggesting an important role for these enzymes in cell growth regulation in embryonic and adult tissues.
Stichworte
signal transduction; sulfatase; knock-out mice; heparan sulfate; glycosaminoglycan; endosulfatase
Erscheinungsjahr
2006
Zeitschriftentitel
BIOCHEMICAL JOURNAL
Band
400
Ausgabe
1
Seite(n)
63-73
ISSN
0264-6021
eISSN
1470-8728
Page URI
https://pub.uni-bielefeld.de/record/1597019

Zitieren

Lamanna WC, Baldwin RJ, Padva M, et al. Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL. 2006;400(1):63-73.
Lamanna, W. C., Baldwin, R. J., Padva, M., Kalus, I., ten Dam, G., van Kuppevelt, T. H., Gallagher, J. T., et al. (2006). Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL, 400(1), 63-73. https://doi.org/10.1042/BJ20060848
Lamanna, William C., Baldwin, Rebecca J., Padva, Michael, Kalus, Ina, ten Dam, Gerdy, van Kuppevelt, Toin H., Gallagher, John T., von Figura, Kurt, Dierks, Thomas, and Merry, Catherine L. R. 2006. “Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity”. BIOCHEMICAL JOURNAL 400 (1): 63-73.
Lamanna, W. C., Baldwin, R. J., Padva, M., Kalus, I., ten Dam, G., van Kuppevelt, T. H., Gallagher, J. T., von Figura, K., Dierks, T., and Merry, C. L. R. (2006). Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL 400, 63-73.
Lamanna, W.C., et al., 2006. Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL, 400(1), p 63-73.
W.C. Lamanna, et al., “Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity”, BIOCHEMICAL JOURNAL, vol. 400, 2006, pp. 63-73.
Lamanna, W.C., Baldwin, R.J., Padva, M., Kalus, I., ten Dam, G., van Kuppevelt, T.H., Gallagher, J.T., von Figura, K., Dierks, T., Merry, C.L.R.: Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity. BIOCHEMICAL JOURNAL. 400, 63-73 (2006).
Lamanna, William C., Baldwin, Rebecca J., Padva, Michael, Kalus, Ina, ten Dam, Gerdy, van Kuppevelt, Toin H., Gallagher, John T., von Figura, Kurt, Dierks, Thomas, and Merry, Catherine L. R. “Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity”. BIOCHEMICAL JOURNAL 400.1 (2006): 63-73.

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