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Thematische Bibliographien / Matrice extracellulare / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Matrice extracellulare“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 11. März 2023

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1

Scolozzi, C. "Aspetti biomolecolari della malattia renale policistica (PKD)." Giornale di Clinica Nefrologica e Dialisi 24, no. 4 (2018): 92–94. http://dx.doi.org/10.33393/gcnd.2012.1182.

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La malattia renale policistica autosomica dominante (ADPKD) è la più comune malattia genetica renale, con incidenza stimata di fra 1:400 e 1:1.000 e causata da mutazioni genetiche di PKD1 (85%) o PKD2 (15%). La caratteristica principale di ADPKD è la presenza di cisti multiple piene di liquido che si ingrandiscono nel tempo. L'espansione e l'iniziazione delle cisti è un complesso processo caratterizzato da anomalie nella proliferazione cellulare, nella secrezione di fluidi, nella formazione della matrice extracellulare e nella polarità delle cellule. Attualmente le strategie terapeutiche maggi

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2

Salaffi, F., M. Carotti, and C. Cervini. "Modificazioni morfo-funzionali della cartilagine nella senescenza e nell'osteoartrosi." Rivista di Neuroradiologia 7, no. 3_suppl (1994): 25–36. http://dx.doi.org/10.1177/19714009940070s305.

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La cartilagine articolare è un tessuto connettivo avascolare, aneurale che ricopre le superfici articolari. La funzione di assorbimento delle sollecitazioni meccaniche, a protezione dell'osso subcondrale, rende la supeficie articolare idonea a sostenere il carico. Le funzioni inerenti le modalità di assorbimento della sollecitazione meccanica, che fanno sì che la deformazione sia reversibile, dipendono in larga parte dalle caratteristiche della cartilagine, intesa come struttura altamente organizzata. Nell'osteoartrosi umana e nei suoi modelli animali l'alterazione strutturale dei proteoglican

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3

Masola, V., S. Granata, M. Proglio, G. Gambaro, A. Lupo, and G. Zaza. "Eparanasi: un nuovo biomarker di fibrosi e un potenziale target farmacologico per ridurre la progressione del danno renale cronico." Giornale di Clinica Nefrologica e Dialisi 24, no. 2 (2018): 10–15. http://dx.doi.org/10.33393/gcnd.2012.1131.

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Il trattamento poli-farmacologico ha determinato, nel corso degli anni, un significativo rallentamento della progressione della malattia renale cronica verso lo stadio di uremia terminale, ma siamo ancora distanti dallo sviluppo di interventi terapeutici in grado di bloccare questo inesorabile e irreversibile processo. Studi clinico-patologici hanno chiaramente dimostrato che il principale elemento coinvolto nel danno renale è la fibrosi tubulo-interstiziale e che il meccanismo patogenetico alla base di questa condizione ha inizio in larga parte nel compartimento tubulare. In particolare, il p

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4

Farina, L., L. Milanesi, E. Ciceri, et al. "Distrofia muscolare congenita con deficit di merosina: Studio RM in 5 pazienti." Rivista di Neuroradiologia 10, no. 2_suppl (1997): 240. http://dx.doi.org/10.1177/19714009970100s2108.

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Recentemente in un certo numero di pazienti con distrofia muscolare congenita (CDM) classica è stato individuato un deficit di merosina, proteina che oltre ad essere responsabile del legame tra la distrofina e la matrice extracellulare sarebbe anche implicata nella crescita del neurite e nella migrazione delle cellule di Schwann. In tutti questi pazienti è presente una grave compromissione della muscolatura scheletrica con ipotonia e impossibilità a raggiungere una deambulazione autonoma e, nonostante l'assenza di una sintomatologia riferibile a danno del SNC, sono state costantemente evidenzi

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5

Salmon, Hélène, and Emmanuel Donnadieu. "La matrice extracellulaire." médecine/sciences 28, no. 10 (2012): 824–26. http://dx.doi.org/10.1051/medsci/20122810009.

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6

Michel, J. B., and G. Loirand. "« Adhésion et matrice extracellulaire »." Archives des Maladies du Coeur et des Vaisseaux - Pratique 2005, no. 141 (2005): 38. http://dx.doi.org/10.1016/s1261-694x(05)88121-0.

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7

Jacob, Marie-Paule. "Matrice extracellulaire et vieillissement vasculaire." médecine/sciences 22, no. 3 (2006): 273–78. http://dx.doi.org/10.1051/medsci/2006223273.

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8

Hornebeck, William, Hervé Emonard, François-Xavier Maquart, and Georges Bellon. "Protéolyse dirigée par la matrice extracellulaire." Journal de la Société de Biologie 197, no. 1 (2003): 25–30. http://dx.doi.org/10.1051/jbio/2003197010025.

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9

Ricard-Blum, Sylvie, and Frank Gondelaud. "De la matrice extracellulaire au noyau." Biologie Aujourd'hui 210, no. 1 (2016): 37–44. http://dx.doi.org/10.1051/jbio/2016007.

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10

de Jaeger, C., and P. Cherin. "Matrice extracellulaire, physiologie et vieillissement vasculaire." Médecine & Longévité 4, no. 1 (2012): 41–53. http://dx.doi.org/10.1016/j.mlong.2012.02.002.

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11

Chelluri, Lakshmi Kiran. "Stem Cells and Extracellular Matrices." Colloquium Series on Stem Cell Biology 1, no. 1 (2012): 1–84. http://dx.doi.org/10.4199/c00053ed1v01y201204scb001.

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12

Comper, Wayne D., Roderick P. W. Williams, and Oliver Zamparo. "Water Transport in Extracellular Matrices." Connective Tissue Research 25, no. 2 (1990): 89–102. http://dx.doi.org/10.3109/03008209009006984.

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13

ISHIKAWA, Osamu. "Extracellular Matrices in the Dermis." Kobunshi 47, no. 10 (1998): 759. http://dx.doi.org/10.1295/kobunshi.47.759.

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14

HAUSMAN, R. "Ocular extracellular matrices in development." Progress in Retinal and Eye Research 26, no. 2 (2007): 162–88. http://dx.doi.org/10.1016/j.preteyeres.2006.11.001.

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15

Ruoslahti, E., E. G. Hayman, and M. D. Pierschbacher. "Extracellular matrices and cell adhesion." Arteriosclerosis: An Official Journal of the American Heart Association, Inc. 5, no. 6 (1985): 581–94. http://dx.doi.org/10.1161/01.atv.5.6.581.

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16

Lelongt, Brigitte, Pierre Ronco, and Rémi Piedagnel. "Métalloprotéases matricielles : infidélités à la matrice extracellulaire." médecine/sciences 18, no. 5 (2002): 519–21. http://dx.doi.org/10.1051/medsci/2002185519.

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17

Gaill, Francoise, Rémy Mosseri, Christine Brigant, and Monique Conceicao. "Modelisation 3D de matrices extracellulaires." Biology of the Cell 63, S1 (1988): 31–31. http://dx.doi.org/10.1016/0248-4900(88)90216-x.

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18

Putnam, Andrew J., and David J. Mooney. "Tissue engineering using synthetic extracellular matrices." Nature Medicine 2, no. 7 (1996): 824–26. http://dx.doi.org/10.1038/nm0796-824.

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19

Lee, Myeongwoo, Indu P. Christopherson, Jeffrey M. Lehman, Cory J. Bennett, and H. Tak Cheung. "Comparison of bone marrow extracellular matrices." Biochimica et Biophysica Acta (BBA) - General Subjects 1428, no. 2-3 (1999): 300–304. http://dx.doi.org/10.1016/s0304-4165(99)00083-5.

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20

Fonseca, Keila B., Pedro L. Granja, and Cristina C. Barrias. "Engineering proteolytically-degradable artificial extracellular matrices." Progress in Polymer Science 39, no. 12 (2014): 2010–29. http://dx.doi.org/10.1016/j.progpolymsci.2014.07.003.

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21

Comper, W. D., L. Pratt, C. J. Handley, and G. S. Harper. "Cell transport in model extracellular matrices." Archives of Biochemistry and Biophysics 252, no. 1 (1987): 60–70. http://dx.doi.org/10.1016/0003-9861(87)90008-7.

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22

Peters, M. C., and D. J. Mooney. "Synthetic Extracellular Matrices for Cell Transplantaton." Materials Science Forum 250 (September 1997): 43–52. http://dx.doi.org/10.4028/www.scientific.net/msf.250.43.

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23

Sarikaya, Ayda, Rae Record, Ching-Ching Wu, Bob Tullius, Stephen Badylak, and Michael Ladisch. "Antimicrobial Activity Associated with Extracellular Matrices." Tissue Engineering 8, no. 1 (2002): 63–71. http://dx.doi.org/10.1089/107632702753503063.

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24

Leach, J. Kent, and David J. Mooney. "Synthetic Extracellular Matrices for Tissue Engineering." Pharmaceutical Research 25, no. 5 (2008): 1209–11. http://dx.doi.org/10.1007/s11095-008-9541-3.

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25

Madl, Christopher M., and Sarah C. Heilshorn. "Bioorthogonal Strategies for Engineering Extracellular Matrices." Advanced Functional Materials 28, no. 11 (2018): 1706046. http://dx.doi.org/10.1002/adfm.201706046.

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26

Jooken, Stijn, Olivier Deschaume, and Carmen Bartic. "Nanocomposite Hydrogels as Functional Extracellular Matrices." Gels 9, no. 2 (2023): 153. http://dx.doi.org/10.3390/gels9020153.

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Over recent years, nano-engineered materials have become an important component of artificial extracellular matrices. On one hand, these materials enable static enhancement of the bulk properties of cell scaffolds, for instance, they can alter mechanical properties or electrical conductivity, in order to better mimic the in vivo cell environment. Yet, many nanomaterials also exhibit dynamic, remotely tunable optical, electrical, magnetic, or acoustic properties, and therefore, can be used to non-invasively deliver localized, dynamic stimuli to cells cultured in artificial ECMs in three dimensi

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27

Jacob, M. P. "Remodelage de la matrice extracellulaire en pathologie vasculaire." Annales de Pathologie 26 (November 2006): 48–49. http://dx.doi.org/10.1016/s0242-6498(06)78373-0.

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28

Nusgens, B. V. "Acide hyaluronique et matrice extracellulaire : une molécule primitive ?" Annales de Dermatologie et de Vénéréologie 137 (April 2010): S3—S8. http://dx.doi.org/10.1016/s0151-9638(10)70002-8.

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29

Horn, Eric M., Michael Beaumont, Xiao Zheng Shu, et al. "Influence of cross-linked hyaluronic acid hydrogels on neurite outgrowth and recovery from spinal cord injury." Journal of Neurosurgery: Spine 6, no. 2 (2007): 133–40. http://dx.doi.org/10.3171/spi.2007.6.2.133.

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Object Therapies that use bioactive materials as replacement extracellular matrices may hold the potential to mitigate the inhibition of regeneration observed after central nervous system trauma. Hyaluronic acid (HA), a nonsulfated glycosaminoglycan ubiquitous in all tissues, was investigated as a potential neural tissue engineering matrix. Methods Chick dorsal root ganglia were cultured in 3D hydrogel matrices composed of cross-linked thiol-modified HA or fibrin. Samples were cultured and images were acquired at 48-, 60-, and 192-hour time points. Images of all samples were analyzed at 48 hou

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30

McDonald, J. A. "Receptors for extracellular matrix components." American Journal of Physiology-Lung Cellular and Molecular Physiology 257, no. 6 (1989): L331—L337. http://dx.doi.org/10.1152/ajplung.1989.257.6.l331.

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The extracellular matrix determines the shape and function of multicellular organisms and permits orderly repair after injury. Although the inherent self-assembly properties of many extracellular matrix components such as collagen and elastin foster their deposition and supramolecular organization, cells ultimately dictate the location and composition of regional matrices. These matrices in turn communicate with cells and regulate their attachment, movement, growth, and gene expression. This complex interaction between cells and their matrix is mediated via specific cellular receptors for matr

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31

Hoshiba, Takashi, Mai Wakejima, Chong-Su Cho, Goshi Shiota, and Toshihiro Akaike. "Different regulation of hepatocyte behaviors between natural extracellular matrices and synthetic extracellular matrices by hepatocyte growth factor." Journal of Biomedical Materials Research Part A 85A, no. 1 (2008): 228–35. http://dx.doi.org/10.1002/jbm.a.31571.

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32

Gaill, Françoise, and Rémy Mosseri. "Ordre quasicristallin dans les matrices extracellulaires." Acta Biotheoretica 40, no. 2-3 (1992): 261–67. http://dx.doi.org/10.1007/bf00168154.

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33

Ros, Manon, Frédéric Bard, and Frédéric Saltel. "La réduction des ponts disulfures de la matrice extracellulaire." médecine/sciences 37, no. 4 (2021): 322–24. http://dx.doi.org/10.1051/medsci/2021025.

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34

Cohen, Jennifer D., and Meera V. Sundaram. "C. elegans Apical Extracellular Matrices Shape Epithelia." Journal of Developmental Biology 8, no. 4 (2020): 23. http://dx.doi.org/10.3390/jdb8040023.

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Apical extracellular matrices (aECMs) coat exposed surfaces of epithelia to shape developing tissues and protect them from environmental insults. Despite their widespread importance for human health, aECMs are poorly understood compared to basal and stromal ECMs. The nematode Caenorhabditis elegans contains a variety of distinct aECMs, some of which share many of the same types of components (lipids, lipoproteins, collagens, zona pellucida domain proteins, chondroitin glycosaminoglycans and proteoglycans) with mammalian aECMs. These aECMs include the eggshell, a glycocalyx-like pre-cuticle, bo

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35

BANACU, Mihail, Bogdan SOCEA, Adrian PELINARU, and Ioan LASCAR. "Extracellular Matrices In Gynecological Surgery – Literature Review." Archives of the Balkan Medical Union 55, no. 2 (2020): 304–11. http://dx.doi.org/10.31688/abmu.2020.55.2.14.

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36

Derwin, K., A. Baker, and J. Iannotti. "Natural extracellular matrices for tendon tissue engineering." Journal of Biomechanics 39 (January 2006): S59. http://dx.doi.org/10.1016/s0021-9290(06)83118-0.

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37

Serban, Monica A., and Glenn D. Prestwich. "Modular extracellular matrices: Solutions for the puzzle." Methods 45, no. 1 (2008): 93–98. http://dx.doi.org/10.1016/j.ymeth.2008.01.010.

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38

Kudo, Akira, and Isao Kii. "Periostin function in communication with extracellular matrices." Journal of Cell Communication and Signaling 12, no. 1 (2017): 301–8. http://dx.doi.org/10.1007/s12079-017-0422-6.

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39

Giliam, K. J., A. T. Dowsing, and A. O. Trounson. "Bovine blastocyst culture on extracellular protein matrices." Theriogenology 47, no. 1 (1997): 279. http://dx.doi.org/10.1016/s0093-691x(97)82406-5.

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40

Fissell, William H., Christina L. Hofmann, Nicholas Ferrell, et al. "Solute partitioning and filtration by extracellular matrices." American Journal of Physiology-Renal Physiology 297, no. 4 (2009): F1092—F1100. http://dx.doi.org/10.1152/ajprenal.00162.2009.

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The physiology of glomerular filtration remains mechanistically obscure despite its importance in disease. The correspondence between proteinuria and foot process effacement suggests podocytes as the locus of the filtration barrier. If so, retained macromolecules ought to accumulate at the filtration barrier, an effect called concentration polarization. Literature data indicate macromolecule concentrations decrease from subendothelial to subepithelial glomerular basement membrane (GBM), as would be expected if the GBM were itself the filter. The objective of this study was to obtain insights i

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41

Ehrbar, Martin, Matthias P. Lütolf, Simone C. Rizzi, Jeffrey A. Hubbell, and Franz E. Weber. "Artificial extracellular matrices for bone tissue engineering." Bone 42 (March 2008): S72. http://dx.doi.org/10.1016/j.bone.2007.12.131.

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42

Hummel, Susanna, Andreas Osanger, Tarek M. Bajari, et al. "Extracellular Matrices of the Avian Ovarian Follicle." Journal of Biological Chemistry 279, no. 22 (2004): 23486–94. http://dx.doi.org/10.1074/jbc.m312694200.

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43

Capadona, J. R., T. A. Petrie, K. P. Fears, R. A. Latour, D. M. Collard, and A. J. García. "Surface-Nucleated Assembly of Fibrillar Extracellular Matrices." Advanced Materials 17, no. 21 (2005): 2604–8. http://dx.doi.org/10.1002/adma.200500959.

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44

Hindriks, Georg A., Jan J. Sixma, and Philip G. de Groot. "Ascorbic Acid Increases the Thrombogenicity of Cellular Matrices." Thrombosis and Haemostasis 66, no. 04 (1991): 505–9. http://dx.doi.org/10.1055/s-0038-1646447.

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SummaryWe have studied the influence of ascorbate on extracellular matrix formation in cultured human endothelial cells, smooth muscle cells and fibroblasts and measured the influence of the changed composition of their isolated extracellular matrices on their affinity for platelets. When endothelial cells were grown for a week in the presence of ascorbate, no influence on proline incorporation in their extracellular matrix was found. In accordance, no influence on platelet adhesion or aggregate formation on these matrices was detected. When smooth muscle cells were cultured in the presence of

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45

STANKEVICIUS, VAIDOTAS, GINTAUTAS VASAUSKAS, RIMANTE NOREIKIENE, KAROLINA KUODYTE, MINDAUGAS VALIUS, and KESTUTIS SUZIEDELIS. "Extracellular Matrix-dependent Pathways in Colorectal Cancer Cell Lines Reveal Potential Targets for Anticancer Therapies." Anticancer Research 36, no. 9 (2016): 4559–68. http://dx.doi.org/10.21873/anticanres.11004.

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46

Unsold, C., M. Hyytiainen, L. Bruckner-Tuderman, and J. Keski-Oja. "Latent TGF-beta binding protein LTBP-1 contains three potential extracellular matrix interacting domains." Journal of Cell Science 114, no. 1 (2001): 187–97. http://dx.doi.org/10.1242/jcs.114.1.187.

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Latent TGF-beta binding proteins (LTBPs) are components of the extracellular matrix (ECM). They belong to the fibrillin/LTBP-superfamily, and are high molecular weight glycoproteins characterized by EGF-like repeats and 8-Cys repeats. Most LTBPs associate with the small latent forms of TGF-beta. Their roles include to facilitate the secretion of latent TGF-beta and to target it to the ECM. In order to identify new matrix-binding domains of LTBP-1 and to characterize their association with the extracellular matrix, we have produced (in a mammalian expression system) partly overlapping recombina

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47

Laug, Walter E., Mark E. Weinblatt, and Peter A. Jones. "Endothelial Cells Degrade Extracellular Matrix Proteins Produced In Vitro." Thrombosis and Haemostasis 54, no. 02 (1985): 498–502. http://dx.doi.org/10.1055/s-0038-1657882.

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SummaryBovine aortic endothelial cells (BAEC) were grown on extracellular matrices produced by vascular smooth muscle cells or fetal bovine endothelial cells. The glycoprotein components of these complex substrates were degraded through activation of the serum zymogen plasminogen to plasmin, as well as by a plasmino- gen independent protease(s). The plasminogen independent enzyme might be a protease with elastolytic activity since the BAEC digested elastin present in smooth muscle cell derived matrices. The cells also displayed collagenolytic activity on both types of matrices.The addition of

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48

Van der Rest, M. "Biologie du collagène et maladies héréditaires de la matrice extracellulaire." médecine/sciences 3, no. 7 (1987): 411. http://dx.doi.org/10.4267/10608/3707.

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49

Labat-Robert, Jacqueline. "Échange d’informations entre cellules et matrice extracellulaire Influence du vieillissement." Biologie Aujourd'hui 206, no. 2 (2012): 103–9. http://dx.doi.org/10.1051/jbio/2012012.

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50

Goetz, Jacky G., and Miguel Angel Del Pozo. "La cavéoline-1 force le remodelage de la matrice extracellulaire." médecine/sciences 27, no. 11 (2011): 940–44. http://dx.doi.org/10.1051/medsci/20112711009.

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