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Integral membrane heparan sulfate proteoglycans

STEM and diversify

[No authors listed]
GSID: J7znVGS2Fz4J
G David - The FASEB Journal, 1993 - Wiley Online Library

Heparan sulfate is a regulatory polysaccharide. It modulates specific growth factor‐receptor interactions, accelerates the formation of specific proteinase‐proteinase inhibitor complexes, …

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David, G. (1993). Integral membrane heparan sulfate proteoglycans. The FASEB Journal, 7(11), 1023-1030.
David, Guido. "Integral membrane heparan sulfate proteoglycans." The FASEB Journal 7.11 (1993): 1023-1030.
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Hierarchical organization of cartilage proteoglycans.

Macromolecular symposia

Horkay F, Basser PJ, Hecht AM, Geissler E.
PMID: 23565043
Macromol Symp. 2011 Sep;306(1):11-17. doi: 10.1002/masy.201000115.

The hierarchical organization of cartilage proteoglycans is investigated on different length and time scales using osmotic pressure measurements, small angle neutron scattering (SANS), small angle X-ray scattering (SAXS), static and dynamic light scattering and neutron spin echo techniques. Osmotic...

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Horkay F, Basser PJ, Hecht AM, et al. Hierarchical organization of cartilage proteoglycans. Macromol Symp. 2011;306(1):11-17doi: 10.1002/masy.201000115.
Horkay, F., Basser, P. J., Hecht, A. M., & Geissler, E. (2011). Hierarchical organization of cartilage proteoglycans. Macromolecular symposia, 306(1), 11-17. https://doi.org/10.1002/masy.201000115
Horkay, Ferenc, et al. "Hierarchical organization of cartilage proteoglycans." Macromolecular symposia vol. 306,1 (2011): 11-17. doi: https://doi.org/10.1002/masy.201000115
Horkay F, Basser PJ, Hecht AM, Geissler E. Hierarchical organization of cartilage proteoglycans. Macromol Symp. 2011 Sep;306(1):11-17. doi: 10.1002/masy.201000115. PMID: 23565043; PMCID: PMC3615634.
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Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development.

Matrix biology : journal of the International Society for Matrix Biology

Jochmann K, Bachvarova V, Vortkamp A.
PMID: 24726293
Matrix Biol. 2014 Apr;35:239-47. doi: 10.1016/j.matbio.2014.04.001. Epub 2014 Apr 12.

Most elements of the vertebrate skeleton are formed by endochondral ossification. This process is initiated with mesenchymal cells that condense and differentiate into chondrocytes. These undergo several steps of differentiation from proliferating into hypertrophic chondrocytes, which are subsequently replaced...

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Jochmann K, Bachvarova V, Vortkamp A. Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development. Matrix Biol. 2014;35:239-47doi: 10.1016/j.matbio.2014.04.001.
Jochmann, K., Bachvarova, V., & Vortkamp, A. (2014). Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development. Matrix biology : journal of the International Society for Matrix Biology, 35239-47. https://doi.org/10.1016/j.matbio.2014.04.001
Jochmann, Katja, et al. "Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development." Matrix biology : journal of the International Society for Matrix Biology vol. 35 (2014): 239-47. doi: https://doi.org/10.1016/j.matbio.2014.04.001
Jochmann K, Bachvarova V, Vortkamp A. Reprint of: Heparan sulfate as a regulator of endochondral ossification and osteochondroma development. Matrix Biol. 2014 Apr;35:239-47. doi: 10.1016/j.matbio.2014.04.001. Epub 2014 Apr 12. PMID: 24726293.
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Molecular mechanisms of inherited thoracic aortic disease - from gene variant to surgical aneurysm.

Biophysical reviews

Robertson E, Dilworth C, Lu Y, Hambly B, Jeremy R.
PMID: 28509973
Biophys Rev. 2015 Mar;7(1):105-115. doi: 10.1007/s12551-014-0147-1. Epub 2014 Dec 06.

Aortic dissection is a catastrophic event that has a high mortality rate. Thoracic aortic aneurysms are the clinically silent precursor that confers an increased risk of acute aortic dissection. There are several gene mutations that have been identified in...

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Robertson E, Dilworth C, Lu Y, et al. Molecular mechanisms of inherited thoracic aortic disease - from gene variant to surgical aneurysm. Biophys Rev. 2014;7(1):105-115doi: 10.1007/s12551-014-0147-1.
Robertson, E., Dilworth, C., Lu, Y., Hambly, B., & Jeremy, R. (2015). Molecular mechanisms of inherited thoracic aortic disease - from gene variant to surgical aneurysm. Biophysical reviews, 7(1), 105-115. https://doi.org/10.1007/s12551-014-0147-1
Robertson, Elizabeth, et al. "Molecular mechanisms of inherited thoracic aortic disease - from gene variant to surgical aneurysm." Biophysical reviews vol. 7,1 (2015): 105-115. doi: https://doi.org/10.1007/s12551-014-0147-1
Robertson E, Dilworth C, Lu Y, Hambly B, Jeremy R. Molecular mechanisms of inherited thoracic aortic disease - from gene variant to surgical aneurysm. Biophys Rev. 2015 Mar;7(1):105-115. doi: 10.1007/s12551-014-0147-1. Epub 2014 Dec 06. PMID: 28509973; PMCID: PMC5425748.
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Glucosamine exposure reduces proteoglycan synthesis in primary human endothelial cells in vitro.

Food & nutrition research

Reine TM, Jenssen TG, Kolset SO.
PMID: 27667774
Food Nutr Res. 2016 Sep 23;60:32615. doi: 10.3402/fnr.v60.32615. eCollection 2016.

PURPOSE: Glucosamine (GlcN) supplements are promoted for medical reasons, for example, for patients with arthritis and other joint-related diseases. Oral intake of GlcN is followed by uptake in the intestine, transport in the circulation and thereafter delivery to chondrocytes....

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Reine TM, Jenssen TG, Kolset SO. Glucosamine exposure reduces proteoglycan synthesis in primary human endothelial cells in vitro. Food Nutr Res. 2016;60:32615doi: 10.3402/fnr.v60.32615.
Reine, T. M., Jenssen, T. G., & Kolset, S. O. (2016). Glucosamine exposure reduces proteoglycan synthesis in primary human endothelial cells in vitro. Food & nutrition research, 6032615. https://doi.org/10.3402/fnr.v60.32615
Reine, Trine M, et al. "Glucosamine exposure reduces proteoglycan synthesis in primary human endothelial cells in vitro." Food & nutrition research vol. 60 (2016): 32615. doi: https://doi.org/10.3402/fnr.v60.32615
Reine TM, Jenssen TG, Kolset SO. Glucosamine exposure reduces proteoglycan synthesis in primary human endothelial cells in vitro. Food Nutr Res. 2016 Sep 23;60:32615. doi: 10.3402/fnr.v60.32615. eCollection 2016. PMID: 27667774; PMCID: PMC5035772.
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UP3005, a Botanical Composition Containing Two Standardized Extracts of Uncaria gambir and Morus alba, Improves Pain Sensitivity and Cartilage Degradations in Monosodium Iodoacetate-Induced Rat OA Disease Model.

Evidence-based complementary and alternative medicine : eCAM

Yimam M, Lee YC, Kim TW, Moore B, Jiao P, Hong M, Kim HJ, Nam JB, Kim MR, Oh JS, Cleveland S, Hyun EJ, Chu M, Jia Q.
PMID: 25802546
Evid Based Complement Alternat Med. 2015;2015:785638. doi: 10.1155/2015/785638. Epub 2015 Feb 23.

Osteoarthritis (OA) is a multifactorial disease primarily noted by cartilage degradation in association with inflammation that causes significant morbidity, joint pain, stiffness, and limited mobility. Present-day management of OA is inadequate due to the lack of principal therapies proven...

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Yimam M, Lee YC, Kim TW, et al. UP3005, a Botanical Composition Containing Two Standardized Extracts of Uncaria gambir and Morus alba, Improves Pain Sensitivity and Cartilage Degradations in Monosodium Iodoacetate-Induced Rat OA Disease Model. Evid Based Complement Alternat Med. 2015;2015:785638doi: 10.1155/2015/785638.
Yimam, M., Lee, Y. C., Kim, T. W., Moore, B., Jiao, P., Hong, M., Kim, H. J., Nam, J. B., Kim, M. R., Oh, J. S., Cleveland, S., Hyun, E. J., Chu, M., & Jia, Q. (2015). UP3005, a Botanical Composition Containing Two Standardized Extracts of Uncaria gambir and Morus alba, Improves Pain Sensitivity and Cartilage Degradations in Monosodium Iodoacetate-Induced Rat OA Disease Model. Evidence-based complementary and alternative medicine : eCAM, 2015785638. https://doi.org/10.1155/2015/785638
Yimam, Mesfin, et al. "UP3005, a Botanical Composition Containing Two Standardized Extracts of Uncaria gambir and Morus alba, Improves Pain Sensitivity and Cartilage Degradations in Monosodium Iodoacetate-Induced Rat OA Disease Model." Evidence-based complementary and alternative medicine : eCAM vol. 2015 (2015): 785638. doi: https://doi.org/10.1155/2015/785638
Yimam M, Lee YC, Kim TW, Moore B, Jiao P, Hong M, Kim HJ, Nam JB, Kim MR, Oh JS, Cleveland S, Hyun EJ, Chu M, Jia Q. UP3005, a Botanical Composition Containing Two Standardized Extracts of Uncaria gambir and Morus alba, Improves Pain Sensitivity and Cartilage Degradations in Monosodium Iodoacetate-Induced Rat OA Disease Model. Evid Based Complement Alternat Med. 2015;2015:785638. doi: 10.1155/2015/785638. Epub 2015 Feb 23. PMID: 25802546; PMCID: PMC4353658.
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Matricryptins Network with Matricellular Receptors at the Surface of Endothelial and Tumor Cells.

Frontiers in pharmacology

Ricard-Blum S, Vallet SD.
PMID: 26869928
Front Pharmacol. 2016 Feb 04;7:11. doi: 10.3389/fphar.2016.00011. eCollection 2016.

The extracellular matrix (ECM) is a source of bioactive fragments called matricryptins or matrikines resulting from the proteolytic cleavage of extracellular proteins (e.g., collagens, elastin, and laminins) and proteoglycans (e.g., perlecan). Matrix metalloproteinases (MMPs), cathepsins, and bone-morphogenetic protein-1 release...

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Ricard-Blum S, Vallet SD. Matricryptins Network with Matricellular Receptors at the Surface of Endothelial and Tumor Cells. Front Pharmacol. 2016;7:11doi: 10.3389/fphar.2016.00011.
Ricard-Blum, S., & Vallet, S. D. (2016). Matricryptins Network with Matricellular Receptors at the Surface of Endothelial and Tumor Cells. Frontiers in pharmacology, 711. https://doi.org/10.3389/fphar.2016.00011
Ricard-Blum, Sylvie, and Vallet, Sylvain D. "Matricryptins Network with Matricellular Receptors at the Surface of Endothelial and Tumor Cells." Frontiers in pharmacology vol. 7 (2016): 11. doi: https://doi.org/10.3389/fphar.2016.00011
Ricard-Blum S, Vallet SD. Matricryptins Network with Matricellular Receptors at the Surface of Endothelial and Tumor Cells. Front Pharmacol. 2016 Feb 04;7:11. doi: 10.3389/fphar.2016.00011. eCollection 2016. PMID: 26869928; PMCID: PMC4740388.
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ESM-1 siRNA Knockdown Decreased Migration and Expression of CXCL3 in Prostate Cancer Cells.

International journal of biomedical science : IJBS

Rebollo J, Geliebter J, Reyes N.
PMID: 28533735
Int J Biomed Sci. 2017 Mar;13(1):35-42.

Endothelial cell-specific molecule-1 (ESM-1), also known as endocan, is a soluble proteoglycan expressed by the vascular endothelium, which also circulates in the bloodstream. Inflammatory cytokines and proangiogenic growth factors increase its expression, and increased serum levels have been reported...

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Rebollo J, Geliebter J, Reyes N. ESM-1 siRNA Knockdown Decreased Migration and Expression of CXCL3 in Prostate Cancer Cells. Int J Biomed Sci. 2017;13(1):35-42
Rebollo, J., Geliebter, J., & Reyes, N. (2017). ESM-1 siRNA Knockdown Decreased Migration and Expression of CXCL3 in Prostate Cancer Cells. International journal of biomedical science : IJBS, 13(1), 35-42.
Rebollo, Juan, et al. "ESM-1 siRNA Knockdown Decreased Migration and Expression of CXCL3 in Prostate Cancer Cells." International journal of biomedical science : IJBS vol. 13,1 (2017): 35-42.
Rebollo J, Geliebter J, Reyes N. ESM-1 siRNA Knockdown Decreased Migration and Expression of CXCL3 in Prostate Cancer Cells. Int J Biomed Sci. 2017 Mar;13(1):35-42. PMID: 28533735; PMCID: PMC5422643.
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The advancements of heparanase in fibrosis.

International journal of molecular epidemiology and genetics

Lv Q, Zeng J, He L.
PMID: 28078057
Int J Mol Epidemiol Genet. 2016 Nov 30;7(4):137-140. eCollection 2016.

Fibrosis is the endpoint in many chronic inflammatory diseases and is defined as an abnormal accumulation of extracellular matrix components. Fibrosis can affect almost any tissue, especially heart, lung, liver, and kidney, and numerous studies have been conducted to...

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Lv Q, Zeng J, He L. The advancements of heparanase in fibrosis. Int J Mol Epidemiol Genet. 2016;7(4):137-140
Lv, Q., Zeng, J., & He, L. (2016). The advancements of heparanase in fibrosis. International journal of molecular epidemiology and genetics, 7(4), 137-140.
Lv, Qianying, et al. "The advancements of heparanase in fibrosis." International journal of molecular epidemiology and genetics vol. 7,4 (2016): 137-140.
Lv Q, Zeng J, He L. The advancements of heparanase in fibrosis. Int J Mol Epidemiol Genet. 2016 Nov 30;7(4):137-140. eCollection 2016. PMID: 28078057; PMCID: PMC5218871.
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Hepcidin antagonists for potential treatments of disorders with hepcidin excess.

Frontiers in pharmacology

Poli M, Asperti M, Ruzzenenti P, Regoni M, Arosio P.
PMID: 24808863
Front Pharmacol. 2014 Apr 28;5:86. doi: 10.3389/fphar.2014.00086. eCollection 2014.

The discovery of hepcidin clarified the basic mechanism of the control of systemic iron homeostasis. Hepcidin is mainly produced by the liver as a propeptide and processed by furin into the mature active peptide. Hepcidin binds ferroportin, the only...

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Poli M, Asperti M, Ruzzenenti P, et al. Hepcidin antagonists for potential treatments of disorders with hepcidin excess. Front Pharmacol. 2014;5:86doi: 10.3389/fphar.2014.00086.
Poli, M., Asperti, M., Ruzzenenti, P., Regoni, M., & Arosio, P. (2014). Hepcidin antagonists for potential treatments of disorders with hepcidin excess. Frontiers in pharmacology, 586. https://doi.org/10.3389/fphar.2014.00086
Poli, Maura, et al. "Hepcidin antagonists for potential treatments of disorders with hepcidin excess." Frontiers in pharmacology vol. 5 (2014): 86. doi: https://doi.org/10.3389/fphar.2014.00086
Poli M, Asperti M, Ruzzenenti P, Regoni M, Arosio P. Hepcidin antagonists for potential treatments of disorders with hepcidin excess. Front Pharmacol. 2014 Apr 28;5:86. doi: 10.3389/fphar.2014.00086. eCollection 2014. PMID: 24808863; PMCID: PMC4009444.
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Spatial mapping of proteoglycan content in articular cartilage using near-infrared (NIR) spectroscopy.

Biomedical optics express

Afara IO, Moody H, Singh S, Prasadam I, Oloyede A.
PMID: 25657883
Biomed Opt Express. 2014 Dec 15;6(1):144-54. doi: 10.1364/BOE.6.000144. eCollection 2015 Jan 01.

Diagnosis of articular cartilage pathology in the early disease stages using current clinical diagnostic imaging modalities is challenging, particularly because there is often no visible change in the tissue surface and matrix content, such as proteoglycans (PG). In this...

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Afara IO, Moody H, Singh S, et al. Spatial mapping of proteoglycan content in articular cartilage using near-infrared (NIR) spectroscopy. Biomed Opt Express. 2014;6(1):144-54doi: 10.1364/BOE.6.000144.
Afara, I. O., Moody, H., Singh, S., Prasadam, I., & Oloyede, A. (2015). Spatial mapping of proteoglycan content in articular cartilage using near-infrared (NIR) spectroscopy. Biomedical optics express, 6(1), 144-54. https://doi.org/10.1364/BOE.6.000144
Afara, Isaac O, et al. "Spatial mapping of proteoglycan content in articular cartilage using near-infrared (NIR) spectroscopy." Biomedical optics express vol. 6,1 (2015): 144-54. doi: https://doi.org/10.1364/BOE.6.000144
Afara IO, Moody H, Singh S, Prasadam I, Oloyede A. Spatial mapping of proteoglycan content in articular cartilage using near-infrared (NIR) spectroscopy. Biomed Opt Express. 2014 Dec 15;6(1):144-54. doi: 10.1364/BOE.6.000144. eCollection 2015 Jan 01. PMID: 25657883; PMCID: PMC4317110.
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Neuropilin-1 and heparan sulfate proteoglycans cooperate in cellular uptake of nanoparticles functionalized by cationic cell-penetrating peptides.

Science advances

Pang HB, Braun GB, Ruoslahti E.
PMID: 26601141
Sci Adv. 2015 Nov 06;1(10):e1500821. doi: 10.1126/sciadv.1500821. eCollection 2015 Nov.

Cell-penetrating peptides (CPPs) have been widely used to deliver nanomaterials and other types of macromolecules into mammalian cells for therapeutic and diagnostic use. Cationic CPPs that bind to heparan sulfate (HS) proteoglycans on the cell surface induce potent endocytosis;...

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Pang HB, Braun GB, Ruoslahti E. Neuropilin-1 and heparan sulfate proteoglycans cooperate in cellular uptake of nanoparticles functionalized by cationic cell-penetrating peptides. Sci Adv. 2015;1(10):e1500821doi: 10.1126/sciadv.1500821.
Pang, H. B., Braun, G. B., & Ruoslahti, E. (2015). Neuropilin-1 and heparan sulfate proteoglycans cooperate in cellular uptake of nanoparticles functionalized by cationic cell-penetrating peptides. Science advances, 1(10), e1500821. https://doi.org/10.1126/sciadv.1500821
Pang, Hong-Bo, et al. "Neuropilin-1 and heparan sulfate proteoglycans cooperate in cellular uptake of nanoparticles functionalized by cationic cell-penetrating peptides." Science advances vol. 1,10 (2015): e1500821. doi: https://doi.org/10.1126/sciadv.1500821
Pang HB, Braun GB, Ruoslahti E. Neuropilin-1 and heparan sulfate proteoglycans cooperate in cellular uptake of nanoparticles functionalized by cationic cell-penetrating peptides. Sci Adv. 2015 Nov 06;1(10):e1500821. doi: 10.1126/sciadv.1500821. eCollection 2015 Nov. PMID: 26601141; PMCID: PMC4640594.
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Showing 1 to 12 of 1032 entries