Pregled bibliografske jedinice broj: 901629
CXCL12/SDF-1 Stimulates Megakaryocyte beta-1, 4- Galactosyltransferase 1 Activity to Enhance Platelet Production in Vivo
CXCL12/SDF-1 Stimulates Megakaryocyte beta-1, 4- Galactosyltransferase 1 Activity to Enhance Platelet Production in Vivo // Experimental Biology Meeting
Boston (MA), Sjedinjene Američke Države, 2015. str. 71922-71922 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 901629 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
CXCL12/SDF-1 Stimulates Megakaryocyte beta-1, 4- Galactosyltransferase 1 Activity to Enhance Platelet Production in Vivo
Autori
Silvia Giannini, Max Adelman, Antonija Jurak Begonja and Karin Hoffmeister
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
Experimental Biology Meeting
Mjesto i datum
Boston (MA), Sjedinjene Američke Države, 28.03.2015. - 01.04.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
SDF-1, thrombopoiesis, Galactosyltransferase 1
Sažetak
Platelet recovery following bone marrow (BM) transplant and chemotherapy is crucial to prevent bleeding complications. The chemokine SDF-1 promotes megakaryocyte (MK) migration towards BM sinusoids increasing platelet production. Here we show that SDF-1 upregulates expression of the glycan structure Type-2- Lactosaminoglycan (LacNAc), synthesized by β4Galactosyltransferase1 (β4galt1). We hypothesized that SDF-1 increases LacNAc synthesis promoting platelet production. Supporting this hypothesis, β4galt1–/– mice had severe macrothrombocytopenia (80% reduction) with increased BMMK numbers (35%), which localized poorly with BM sinusoids (50%), compared to WT MKs (72%). β4galt1–/– hematopoietic stem cells (HSCs) transplanted into lethally irradiated WT mice restored BMMKs, which failed to migrate to sinusoids and produce circulating platelets. We next treated WT and β4galt1–/– mice with the myeloablative chemotherapeutic agent 5-Fluorouracil (5-FU), which decreased platelet counts by 50% in both phenotypes. SDF-1 injections increased platelet counts by 70% in 5-FU treated WT mice but not in β4galt1–/– mice. Importantly, WT but not β4galt1–/– platelets had increased LacNAc expression after SDF-1 injections.β4galt1–/– BMMKs had increased β1 integrin expression. Expression of laminin, β1 integrin ligand, was upregulated in β4galt1–/– MKs and sinusoids. Our results suggest that SDF-1 upregulates β4GalT1-dependentLacNAc expression promoting MK interaction with BM sinusoids, likely regulating β1 integrin expression and interaction with components of the extracellular matrix, specifically laminin.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Antonija Jurak Begonja
(autor)