Sulfation Patterns Determine Cellular Internalization of Heparin-Like Polysaccharides

被引:35
作者
Raman, Karthik [1 ]
Mencio, Caitlin [2 ]
Desai, Umesh R. [3 ]
Kuberan, Balagurunathan [1 ,2 ,4 ]
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Univ Utah, Interdept Program Neurosci, Salt Lake City, UT 84112 USA
[3] Virginia Commonwealth Univ, Dept Med Chem, Richmond, VA 23284 USA
[4] Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
关键词
heparin; cellular uptake; internalization; nucleus localization; heparan sulfate; heparosan; NUCLEAR-LOCALIZATION; INHIBITION; GROWTH; ANGIOGENESIS;
D O I
10.1021/mp300679a
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Heparin is a highly sulfated polysaccharide that serves biologically relevant roles as an anticoagulant and anticancer agent. While it is well-known that modification of heparin's sulfation pattern can drastically influence its ability to bind growth factors and other extracellular molecules, very little is known about the cellular uptake of heparin and the role sulfation patterns serve in affecting its internalization. In this study, we chemically synthesized several fluorescently labeled heparins consisting of a variety of sulfation patterns. These polysaccharides were thoroughly characterized using anion exchange chromatography and size exclusion chromatography. Subsequently, we utilized flow cytometry and confocal imaging to show that sulfation patterns differentially affect the amount of heparin uptake in multiple cell types. This study provides the first comprehensive analysis of the effect of sulfation pattern on the cellular internalization of heparin or heparan sulfate like polysaccharides. The results of this study expand current knowledge regarding heparin internalization and provide insights into developing more effective heparin-based drug conjugates for applications in intracellular drug delivery.
引用
收藏
页码:1442 / 1449
页数:8
相关论文
共 33 条
[1]   CONTRIBUTION OF 3-O-SULFATED AND 6-O-SULFATED GLUCOSAMINE RESIDUES IN THE HEPARIN-INDUCED CONFORMATIONAL CHANGE IN ANTITHROMBIN-III [J].
ATHA, DH ;
LORMEAU, JC ;
PETITOU, M ;
ROSENBERG, RD ;
CHOAY, J .
BIOCHEMISTRY, 1987, 26 (20) :6454-6461
[2]   Fluorescent-tagged heparan sulfate precursor oligosaccharides to probe the enzymatic action of heparitinase I [J].
Babu, Ponnusamy ;
Kuberan, Balagurunathan .
ANALYTICAL BIOCHEMISTRY, 2010, 396 (01) :124-132
[3]  
Berry D, 2004, CHEM BIOL, V11, P487, DOI 10.1016/j.chembiol.2004.03.023
[4]   Antimetastatic activities of modified heparins: Selectin inhibition by heparin attenuates metastasis [J].
Borsig, Lubor .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 2007, 33 (05) :540-546
[5]   Heparanase Regulates Levels of Syndecan-1 in the Nucleus [J].
Chen, Ligong ;
Sanderson, Ralph D. .
PLOS ONE, 2009, 4 (03)
[6]   EFFECT OF HEPARIN MODIFICATION ON ITS ACTIVITY IN ENHANCING INHIBITION OF THROMBIN BY ANTITHROMBIN-III [J].
DANISHEFSKY, I ;
AHRENS, M ;
KLEIN, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 498 (01) :215-222
[7]  
Engelberg H, 1999, CANCER-AM CANCER SOC, V85, P257, DOI 10.1002/(SICI)1097-0142(19990115)85:2<257::AID-CNCR1>3.0.CO
[8]  
2-2
[9]   HEPARIN STIMULATION OF PLASMINOGEN-ACTIVATOR SECRETION BY MACROPHAGE-LIKE CELL-LINE RAW264.7 - ROLE OF THE SCAVENGER RECEPTOR [J].
FALCONE, DJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 140 (02) :219-226
[10]   ANGIOGENESIS INHIBITION AND TUMOR-REGRESSION CAUSED BY HEPARIN OR A HEPARIN FRAGMENT IN THE PRESENCE OF CORTISONE [J].
FOLKMAN, J ;
LANGER, R ;
LINHARDT, RJ ;
HAUDENSCHILD, C ;
TAYLOR, S .
SCIENCE, 1983, 221 (4612) :719-725