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LSKL, Inhibitor of Thrombospondin TSP-1

Katalog-Nr.GC32728

LSKL, Inhibitor of Thrombospondin TSP-1, ist ein von Latency-Associated Protein (LAP)-TGFβ abgeleitetes Tetrapeptid und ein kompetitiver TGF-β1-Antagonist. LSKL, Inhibitor von Thrombospondin TSP-1 hemmt die Bindung von TSP-1 an LAP und lindert interstitielle Nierenfibrose und Leberfibrose. LSKL, Inhibitor of Thrombospondin TSP-1, unterdrückt die Subarachnoidalfibrose durch Hemmung der TSP-1-vermittelten TGF-β1-Aktivität, verhindert die Entwicklung eines chronischen Hydrozephalus und verbessert langfristige neurokognitive Defekte nach Subarachnoidalblutung (SAB). LSKL, Inhibitor von Thrombospondin TSP-1 kann leicht die Blut-Hirn-Schranke überwinden.

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LSKL, Inhibitor of Thrombospondin TSP-1 Chemische Struktur

Cas No.: 283609-79-0

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5mg
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10mg
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25mg
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Sample solution is provided at 25 µL, 10mM.

Product has been cited by 1 publications

Description Protocol Chemical Properties Product Documents Related Products

LSKL, Inhibitor of Thrombospondin (TSP-1) is a peptide derived from the latency-associated peptide, inhibits thrombospondin (TSP-1) activation of TGF-β and prevents the progression of hepatic damage and fibrosis.

LSKL peptide is able to reduce liver fibrosis by inhibiting TGF-β activation[2].

LSKL (1 mg/kg, i.p.) can easily traverse the blood brain barrier. LSKL peptide also alleviates hydrocephalus and improves long-term cognitive function following SAH. Moreover, LSKL peptide inhibits subarachnoid fibrosis after SAH. LSKL treatment significantly decreases the activation of TGF-β1 in the CSF in comparison with that in the SAH+PBS group[1]. LSKL peptide (30 mg/kg, i.p.) successfully inhibits transforming growth factor (TGF) β-Smad signal activation induced by partial hepatectomy. LSKL peptide successfully attenuates TGF-β-Smad signal activation by antagonizing TSP-1, but not by reducing TSP-1 protein expression. LSKL peptide accelerates hepatocyte proliferation after hepatectomy[3].

[1]. Liao F, et al. LSKL peptide alleviates subarachnoid fibrosis and hydrocephalus by inhibiting TSP1-mediated TGF-β1 signaling activity following subarachnoid hemorrhage in rats. Exp Ther Med. 2016 Oct;12(4):2537-2543. Epub 2016 Aug 31. [2]. Laurent MA, et al. In silico characterization of the interaction between LSKL peptide, a LAP-TGF-beta derived peptide, and ADAMTS1. Comput Biol Chem. 2016 Apr;61:155-61. [3]. Kuroki H, et al. Effect of LSKL peptide on thrombospondin 1-mediated transforming growth factor β signal activation and liver regeneration after hepatectomy in an experimental model. Br J Surg. 2015 Jun;102(7):813-25.

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