• No results found

Therapeutic and imaging potential of peptide agents in cardiocascular disease

N/A
N/A
Protected

Academic year: 2021

Share "Therapeutic and imaging potential of peptide agents in cardiocascular disease"

Copied!
11
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

Therapeutic and imaging potential of peptide agents in cardiocascular

disease

Yu, H.

Citation

Yu, H. (2007, June 21). Therapeutic and imaging potential of peptide agents in cardiocascular disease. Retrieved from https://hdl.handle.net/1887/12090

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden

Downloaded from: https://hdl.handle.net/1887/12090

Note: To cite this publication please use the final published version (if applicable).

(2)

Abbreviations

Abbreviations

SR-AI Scavenger receptor type I CsA Cyclosporin A

ECM Extracellular matrix

FITC Fluorescein 5-isothiocyanate FKBP FK506 binding protein

G(Y)FP Green (yellow) fluorescent protein GPCR G-protein coupled receptor

IL Interleukin

NFAT Nuclear factor of activated T-cells NFNB Nuclear factor kappa B

PDGF-BB Platelet derived growth factor-BB vSMC Vascular smooth muscle cell

ERK Extracellular signal regulated kinase CnA Calcineurin catalytic unit A

CaN Calcineurin

Ldlr Low density lipoprotein receptor

ApoE Apolipoprotein E

PE Phycoerythrin

FACS Fluorescence-activated cell sorting PMA Phorbol 12-myristate 13-acetate AKAP79 A-kinase anchoring protein-79

Cabin-1/cain Calcineurin binding protein-1/calcineurin inhibitory protein DSCR-1 Down’s syndrome critical region-1

CHP Calcineurin-B homology protein GSK3 Glycogen synthase kinase-3

ERK Extracellular signal-regulated kinase GST Glutathione-S-transferase HRP Horseradish Peroxidase HOBt 1-hydroxybezotriazole

TBTU 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate

Fmoc N-(9-fluorenyl)methoxy-carbonyl TGF- Transforming growth factor 

CD40L CD154, CD40 ligand

ISR In-stent restenosis

MMP Matrix metalloproteinase

(3)

- 128 -

(4)

List of publications Full Papers

H. Yu, J. Guo, N. Li, J. Kang, Y. Deng. Pharmacokinetics and bioavailability of ribavirin liposomes in rats. Journal of Shenyang Pharmaceutical University. 2001, 18(5), 320-323 H. Yu, K. Sliedregt, H. Overkleeft, G.A. Van der Marel, Th.J.C. Van Berkel, E.A.L.

Biessen. Therapeutic potential of synthetic peptide inhibitor of nuclear factor of activated T-cells as anti-restenotic agent. Arterioscler Thromb Vasc Biol. 2006, 26: 1531-1537 H. Yu, ThJC Van Berkel, EAL. Biessen. Therapeutic Potential of VIVIT, a selective peptide inhibitor of Nuclear Factor of Activated T-cells, in cardiovascular disorders.

Cardiovascular drug reviews. 2007, 25 (2), 1-13

H. Yu, F.M.E. Segers, P. Prince, Th.J.C. Van Berkel, T. Tanaka, E.A.L. Biessen.

Atherosclerosis Imaging Potential of a Novel Peptide Ligand selective for SR-AI.

(Submitted)

H. Yu, I. Bot, X. Xu, K. Sliedregt, H. Overkleeft, G.A. Van der Marel, Th.J.C. Van Berkel, E.A.L. Biessen. Potent Bipartite Inhibitors of Nuclear Factor of Activated T-Cells with Superior Selectivity Compared with Cyclosporin A (Submitted)

H. Yu, A.M. Woltman, C. van Kooten, P. Boross, S. Verbeek, K. Sliedregt, H. Overkleeft, G.A. Van der Marel, ThJC Van Berkel, E.A.L. Biessen. Targeting CD40 function with a selective phage display derived peptide antagonist. (Manuscript in preparation)

PATENTS:

Biessen EAL, Yu. H and ThJC Van Berkel. SR-AI antagonists. P68106EP00, June 19, 2004 Biessen EAL, Yu. H, K. Sliedregt, H. Overkleeft, G.A. Van der Marel, ThJC Van Berkel.

Selective NFAT inhibitors. P80892NL00, April 18, 2007

Biessen EAL, Yu. H, K. Sliedregt, H. Overkleeft, G.A. Van der Marel, , S. Verbeek, van Kooten C, ThJC Van Berkel. Selective CD40 binding peptide (Submitted)

PUBLISHED ABSTRACTS:

H. Yu, van Kooten C, ThJC Van Berkel, EAL. Biessen. Targeting CD40 function with a selective phage display derived peptide antagonist. (Oral presentation at the AHA Scientific Sessions 2004). Circulation. 2004; 110: III-326

H. Yu, K. Sliedregt, H. Overkleeft, van der Marel G, ThJC Van Berkel, EAL Biessen.

Selective Inhibition of Nuclear Factor of Activated T-cells Signalling by Synthetic VIVIT:

Promise as an Anti-restenotic Agent. (Oral presentation at the AHA Scientific Sessions 2005). Circulation. 2005, 112:II-169

A.O. Kraaijeveld, M.L. Lucerna, R. van Oort, H. Yu, J.W. Jukema, Th.J. Van Berkel, L.J.

de Windt and E.A.L Biessen. Myocyte enhancer factor 2A is a potent regulator of angiogenesis and of erythrocyte extravasation in atherosclerotic plaques. Circulation. 2006, 114:II-103

(5)

- 130 -

(6)

Curriculum Vitae

Curriculum Vitae

Haixiang Yu was born on Nov 26th 1976 in Baotou, Inner Mongolia, P. R.

China. He went to Shenyang Pharmaceutical University in 1994 and had 4 years training in pharmaceutics. From 1998 to 2001, under the supervision of Professor Yingjie Deng, he had three years training in liposome research in the Graduate School of Shenyang Pharmaceutical University and obtained his Master’s Degree in 2001. He then came to Division of Biopharmaceutics of Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University, as a visiting student in Oct, 2001. He had one year training in solid phase organic synthesis and phage display under the supervision of Prof. Dr. Erik AL Biessen. He learned the basic techniques in solid phase peptide synthesis, molecular and cell biology of atherosclerosis.

Starting from Oct 2002, he has been working as a Ph.D. student in the Division of Biopharmaceutics of Leiden/Amsterdam Center for Drug Research (LACDR), Leiden University, under the supervision of Prof. Dr.

Erik AL Biessen and Prof. Dr. Theo J.C. Van Berkel. During his Ph.D training, his research has been mainly focused on development of peptide antagonists and their application in targeted imaging and therapeutic intervention of cardiovascular diseases. Since July 2007, he has been employed as a research associate to continue his research in cardiovascular diseases at the Division of Cardiovascular Medicine, University of Cambridge under the guidance of Professor Martin R Bennett.

(7)

- 132 -

(8)

Appendix Appendix

Color figures

(9)

Appendix

- 134 - PE

DAPI

Overlay

StrepPE-biotin StrepPE-bioPP1 StrepPE-bioPP1+fucoidin

PE

DAPI

Overlay

StrepPE-biotin StrepPE-bioPP1 StrepPE-bioPP1+fucoidin

Chapter 3 Fig. 3C

Chapter 6 Fig. 2J

(10)

Appendix

NF-kB

DAPI

Overlay

Control Ionomycin CsA MCV1

NF-kB

DAPI

Overlay

Control Ionomycin CsA MCV1

Control Ionomycin CsA MCV1

NFAT

CaN

DAPI

Overlay

Control Ionomycin CsA MCV1

NFAT

CaN

DAPI

Overlay

Chapter 6 Fig 3C (upper), 3D (lower)

(11)

Appendix

- 136 -

Referenties

GERELATEERDE DOCUMENTEN

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden Downloaded.

Financial support by the Netherlands Heart Foundation for the publication of this thesis is gratefully acknowledged. The printing of this thesis was also financially supported by

SR-AI, CD36 (SR class B), CD68 (SR class D), lectin-like oxidized LDL receptor (LOX-1, SR class E), scavenger receptors expressed by endothelial cells (SREC, SR class F), and

In search of antagonist specific for SR-AI, we have employed affinity selection of a random phage displayed peptide library on a synthetic receptor comprising the ligand

(C) Binding of the enriched phage pool to human CD40-muIgG was determined in the presence of synthetic peptides encoded by CD40 specific phage clone NP31 (); a scrambled NP31

While HPVIVIT and INCA12 both are weak inhibitors of calcineurin-NFAT interaction, simultaneous targeting of both NFAT recognition sites on calcineurin by MCV1 will result in

In this thesis, we aimed to develop novel peptide ligands by a combined phage display and bioorganic synthesis strategy and to investigate the targeted potential of developed

In hoofdstuk 3 hebben we met succes een nieuwe SR-AI bindend peptide geïdentificeerd door middel van een geavanceerde moleculair biologische techniek, peptide faagdisplay, en