Reactive glial cells: increased stiffness correlates with increased intermediate filament expression

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Bringmann, A., Pannicke, T., Grosche, J., Francke, M., Wiedemann, P., Skatchkov, S. N., Osborne, N. N., & Reichenbach, A. (2006) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2006.05.003 · Cited by 1,967

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Perea, G., Navarrete, M., & Araque, A. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2009.05.001 · Cited by 1,820

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Pekny, M., & Nilsson, M. (2005) · Glia · doi:10.1002/glia.20207 · Cited by 1,611

Neurite branching on deformable substrates

Flanagan, L. A., Ju, Y. S., Marg, B., Osterfield, M., & Janmey, P. A. (2002) · Neuroreport · doi:10.1097/00001756-200212200-00007 · Cited by 759

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Wilhelmsson, U., Bushong, E. A., Price, D. L., Smarr, B. L., Phung, V., Terada, M., Ellisman, M. H., & Pekny, M. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602841103 · Cited by 643 · cited 1×

Viscoelastic properties of individual glial cells and neurons in the CNS

Lu, Y., Franze, K., Seifert, G., Steinhäuser, C., Kirchhoff, F., Wolburg, H., Guck, J. R., Janmey, P. A., Wei, E.-Q., Käs, J. A., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606150103 · Cited by 580

Scanning Probe-Based Frequency-Dependent Microrheology of Polymer Gels and Biological Cells

Mahaffy, R. E., Shih, C.-K. K., MacKintosh, F. C., & Käs, J. A. (2000) · Physical Review Letters · doi:10.1103/physrevlett.85.880 · Cited by 509

Quantitative Analysis of the Viscoelastic Properties of Thin Regions of Fibroblasts Using Atomic Force Microscopy

Mahaffy, R. E., Park, S., Gerde, E., Käs, J. A., & Shih, C.-K. K. (2004) · Biophysical Journal · doi:10.1016/s0006-3495(04)74245-9 · Cited by 460

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Wilhelmsson, U., Li, L., Pekna, M., Berthold, C.-H., Blom, S., Eliasson, C., Renner, O., Bushong, E., Ellisman, M., Morgan, T. E., et al. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0820-04.2004 · Cited by 455

Astrocytes and the regulation of cerebral blood flow

Koehler, R. C., Roman, R. J., & Harder, D. R. (2009) · Trends in Neurosciences · doi:10.1016/j.tins.2008.11.005 · Cited by 439

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Bringmann, A., Unterlauft, J. D., Barth, T., Wiedemann, R., Rehák, M., & Wiedemann, P. (2021) · Experimental Eye Research · doi:10.1016/j.exer.2021.108604 · Cited by 20

In vivo stiffness of multiple sclerosis lesions is similar to that of normal-appearing white matter

Herthum, H., Hetzer, S., Scheel, M., Shahryari, M., Braun, J., Paul, F., & Sack, I. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.10.038 · Cited by 20

Biphasic analysis of rat brain slices under creep indentation shows nonlinear tension-compression behavior

Wang, R., & Sarntinoranont, M. (2018) · Journal of the mechanical behavior of biomedical materials/Journal of mechanical behavior of biomedical materials · doi:10.1016/j.jmbbm.2018.08.043 · Cited by 19

Cellular changes at the glia-neuro-vascular interface in definite idiopathic normal pressure hydrocephalus

Eide, P. K. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.981399 · Cited by 18

Inherently slow and weak forward forces of neuronal growth cones measured by a drift‐stabilized atomic force microscope

Fuhs, T., Reuter, L., Vonderhaid, I., Claudepierre, T., & Käs, J. A. (2012) · Cytoskeleton · doi:10.1002/cm.21080 · Cited by 18

The TIR ‐domain‐containing adapter inducing interferon‐β‐dependent signaling cascade plays a crucial role in ischemia–reperfusion‐induced retinal injury, whereas the contribution of the myeloid differentiation primary response 88‐dependent signaling cascade is not as pivotal

Dvoriantchikova, G., Santos, A. R. C., Danek, D. J., Dvoriantchikova, X., & Ivanov, D. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12603 · Cited by 18

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Reichenbach, A., & Bringmann, A. (2015) · Colloquium Series on Neuroglia in Biology and Medicine From Physiology to Disease · doi:10.4199/c00122ed1v01y201412ngl003 · Cited by 18

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Alfasi, A. M., Shulyakov, A. V., & Bigio, M. R. D. (2013) · Journal of neurosurgery · doi:10.3171/2013.7.jns121973 · Cited by 16

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Substrate Elastic Modulus Regulates the Morphology, Focal Adhesions, and α-Smooth Muscle Actin Expression of Retinal Müller Cells

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Attenuation of reactive gliosis in stroke-injured mouse brain does not affect neurogenesis from grafted human iPSC-derived neural progenitors

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Michalski, D., Härtig, W., Krueger, M., Hobohm, C., Käs, J. A., & Fuhs, T. (2015) · Neuroreport · doi:10.1097/wnr.0000000000000395 · Cited by 13

Cell-matrix tension contributes to hypoxia in astrocyte-seeded viscoelastic hydrogels composed of collagen and hyaluronan

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Foveal regeneration after resolution of cystoid macular edema without and with internal limiting membrane detachment: presumed role of glial cells for foveal structure stabilization

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Åkerström, B., Cederlund, M., Bergwik, J., Manouchehrian, O., Arnér, K. M., Holmgren-Taylor, I., Ghosh, F. K., & Taylor, L. (2017) · Current Eye Research · doi:10.1080/02713683.2016.1254247 · Cited by 9

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Hu, T., Meng, S., Zhang, Q., Song, S., Tan, C., Huang, J., & Chen, D. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00932-1 · Cited by 9

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Carapia, A. K., Martinez-Colin, E. J., Segura-Villalobos, D., Victoria-Chavez, R. Y., Lezama, I., Martínez‐Martínez, E., & Lamas, M. (2023) · ASN NEURO · doi:10.1177/17590914231183272 · Cited by 8

Functional Stem Cell Integration Assessed by Organotypic Slice Cultures

Herlenius, E., Thonabulsombat, C., Forsberg, D., Jäderstad, J., Jäderstad, L. M., Björk, L., & Olivius, P. (2012) · Current Protocols in Stem Cell Biology · doi:10.1002/9780470151808.sc02d13s23 · Cited by 8

Quantifying the Local Mechanical Properties of Cells in a Fibrous Three-Dimensional Microenvironment

Dagro, A. M., Rajbhandari, L., Orrego, S., Kang, S. H., Venkatesan, A., & Ramesh, K. T. (2019) · Biophysical Journal · doi:10.1016/j.bpj.2019.07.042 · Cited by 8

Identifying Hmga2 preserving visual function by promoting a shift of Müller glia cell fate in mice with acute retinal injury

Yin, Z., Ge, L., Cha, Z., Gao, H., Luodan, A., Zeng, Y., Huang, X., Cheng, X., Yao, K., Tao, Z., et al. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-03657-9 · Cited by 7

Towards in vivo differentiation of brain tumor versus normal tissue by means of torsional resonators

Johannsmann, D., Langhoff, A., Bode, B., Mpoukouvalas, K., Heimann, A., Kempski, O. S., & Charalampaki, P. (2012) · Sensors and Actuators A Physical · doi:10.1016/j.sna.2012.10.039 · Cited by 7

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Ghosh, F. K., Arnér, K. M., & Taylor, L. (2015) · Graefe s Archive for Clinical and Experimental Ophthalmology · doi:10.1007/s00417-015-3236-3 · Cited by 6

Reactive Astrocytes, Astrocyte Intermediate Filament Proteins, and Their Role in the Disease Pathogenesis

Pekny, M., Porritt, M. J., de Pablo, Y., Pekna, M., & Wilhelmsson, U. (2012) · Neuromethods · doi:10.1007/978-1-62703-266-7_13 · Cited by 6

Nerve Root Compression Increases Spinal Astrocytic Vimentin in Parallel With Sustained Pain and Endothelial Vimentin in Association With Spinal Vascular Reestablishment

Smith, J. R., Lee, J., & Winkelstein, B. A. (2017) · Spine · doi:10.1097/brs.0000000000002103 · Cited by 6

Predicting local tissue mechanics using immunohistochemistryPreprint

Koser, D. E., Moeendarbary, E., Küerten, S., & Franze, K. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/358119 · Cited by 6

Implications of the glymphatic system in the pathogenesis of normal pressure hydrocephalus: an illustrated scoping review

Costa, M. L., Martinez, D. C., Chen, H. A., Colasurdo, M., & Kan, P. T. M. (2025) · Journal of neurosurgery · doi:10.3171/2024.12.jns2420 · Cited by 7

Deletion of the cell adhesion adaptor protein vinculin disturbs the localization of GFAP in Bergmann glial cells

Winkler, U., Hirrlinger, P., Sestu, M., Wilhelm, F., Besser, S., Zemljic-Harpf, A. E., Ross, R., Bornschein, G., Krügel, U., Ziegler, W., et al. (2013) · Glia · doi:10.1002/glia.22495 · Cited by 3

Curing the brain: in search for new astrocyte-specific therapies

Verkhratsky, A., Lee, C. J., Chun, H., Göritz, C., Harkany, T., Lee, J., Lee, S., Lindskog, M., Koh, W., Mulder, J., et al. (2026) · Experimental & Molecular Medicine · doi:10.1038/s12276-026-01712-4 · Cited by 8

Normal Pressure Hydrocephalus: Revisiting the Hydrodynamics of the Brain

Hakim, F., Jaramillo-Velásquez, D., González, M., Gómez, D. F., Ramón, J. F., & Serrano-Pinzón, M. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.98813 · Cited by 3

Primate fovea

Bringmann, A., & Wiedemann, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90467-4.00001-2 · Cited by 2

Holographic Feedback Controlled Micro-Stereolithography for Constructing Microstructures with Tuned Mechanical Property

Dong, X., Zhao, Y., Zhang, Q., Sun, L., Wang, H., Shi, Q., Huang, Q., & Wang, H. (2024) · International Symposium on Autonomous Systems (ISAS) · doi:10.1109/isas61044.2024.10552462 · Cited by 1

Macular Pucker Staging System and Surgery

Govetto, A., & Radice, P. (2024) · Springer eBooks · doi:10.1007/978-3-031-63508-3_5 · Cited by 1

Immunohistochemical localization of glial fibrillary acidic protein in the retinas of some amphibian, reptilian, birds, and mammals species

Seleem, A. A. (2025) · Journal of Histotechnology · doi:10.1080/01478885.2025.2582277 · Cited by 1

Brillouin microscopic assessment of retinal stiffness during reactive Müller gliosis

Saeidifard, S., Saltykova, I. V., Gerner-Mauro, K. N., Schill, A., Larin, K. V., & Poché, R. A. (2026) · Experimental Eye Research · doi:10.1016/j.exer.2026.110926 · Cited by 1

Spatial Distribution of Cytoskeletal Mechanical Properties in Vascular Smooth Muscle Cells

Jiang, Q., Chen, P., & Li, J. (2015) · Journal of Biomedical Science and Engineering · doi:10.4236/jbise.2015.85033 · Cited by 1

Cell Biology of the Müller Cell

Reichenbach, A., & Bringmann, A. (2012) · Elsevier eBooks · doi:10.1016/b978-1-4557-0737-9.00017-5 · Cited by 1

Oxygen and glucose deprivation on human Müller cells (MIO-M1) and human organotypic retinal cultures (HORCs) in relation to glaucoma

Aldarwesh, A. (2015) · UEA Digital Repository (University of East Anglia) · Cited by 1

Diagnosis

Sean Sanders DVM, P. (2025) · doi:10.1002/9781394245642.ch5 · Cited by 1

Biochemical and biomechanical modulation of the in vitro retina

Taylor, L. (2013) · Lund University Publications (Lund University)

Proteomics of mouse cortex following conditional deletion of Psmc1 proteasomal subunit in neurones

Elkharaz, J. (2013) · Nottingham ePrints (University of Nottingham)

Changes in hippocampal ultrastructure and vimentin expression in rhesus monkeys following selective deep hypothermia and blood occlusion

Li, B., Fu, X., Niu, X., Fan, Y., Xu, W., Zhao, X. X., & Pu, J. (2015) · Genetics and Molecular Research · doi:10.4238/2015.january.30.7

Design, implementation and application of high throughput magnetic tweezers for cell mechanics studies

Chen, L., Fitter, J., & Offenhäusser, A. (2016) · RWTH Publications (RWTH Aachen)

The Role of Stat3 in Mouse Models of Inherited Photoreceptor Degeneration

Jiang, K. (2013) · TSpace (University of Toronto)

Assessment and modulation of gliosis in inherited eye disease and its impact on cell replacement therapy

Graca, A. B. (2017) · UCL Discovery (University College London)

The role of glial cells in a mouse model of inherited retinal dystrophies

Chen, Y. (2019)

Developing a neural implant to enable controlled alterations to brain architecture

Weir, N. (2019) · Nottingham Trent University's Institutional Repository (Nottingham Trent Repository)

Müller Cells: Genii Loci

Валерьевна, Т. М., Gavrilova, S. A., & Иошин, И. Э. (2020) · Human Physiology · doi:10.1134/s0362119720050126

Tractional disorders of the human fovea

Bringmann, A., & Wiedemann, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90467-4.00007-3

References

(2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90467-4.00011-5

Retinal glia

Bringmann, A., & Wiedemann, P. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-90467-4.00003-6

Macular Pucker and Vitreomacular Traction

Williamson, T. H. (2021) · Springer eBooks · doi:10.1007/978-3-030-68769-4_12

Influência de microRNAs na contração e transdiferenciação de células gliais de Müller da retina

Siqueira, P. V. (2023) · doi:10.11606/d.42.2023.tde-24082023-152907

The Role of Müller Cells in Diabetic Retinopathy

Açan, D. (2024) · IntechOpen eBooks · doi:10.5772/intechopen.1006382

Advanced Fibers for Optogenetic Modulation

Du, M., & Zhou, S. (2024) · Wiley eBooks · doi:10.1002/9783527839322.ch7

Idiopathic Normal Pressure Hydrocephalus : Focus on Imaging and Clinical Symptoms

Eleftheriou, A. (2025) · Linköping University medical dissertations · doi:10.3384/9789181180916

Physiological substantiation of the effect of mechanical impact on internal organs (literature review)

Ikhlef, A., Potekhina, Y. P., & Simenko, E. V. (2025) · Russian Osteopathic Journal · doi:10.32885/2220-0975-2025-3-134-150

Case Report: A case of unexplained retinoschisis

Wang, N., Zhang, Y., Yuan, F., Zhao, C., & Zhou, Z. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1546953

Plectin associates with focal adhesions and contributes to cytoskeletal organization and mechanical properties of astrocytes

Furlani, B., Potokar, M., Devoto, V. M. P., Pérez‐Sala, D., Wiche, G., Zorec, R., & Jorgačevski, J. (2025) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00425.2025

Additional file 1 of Identifying Hmga2 preserving visual function by promoting a shift of Müller glia cell fate in mice with acute retinal injury

Yin, Z., Ge, L., Cha, Z., Gao, H., Luodan, A., Zeng, Y., Huang, X., Cheng, X., Yao, K., Tao, Z., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25302992

Panton–Valentine leucocidin colocalized with retinal neurons cells and incited early retinal inflammation through rabbit endophthalmitis and retinal explant models

Liu, X. (2018) · theses.fr (ABES) · doi:10.70675/85bd72dez6353z441bz9566z17070f9d7ddc

Questions émergentes dans l'évaluation du risque rétinien des nouvelles technologies d'éclairement domestique : étude expérimentale

Françon, A. (2023) · theses.fr (ABES) · doi:10.70675/3af0567ez2658z4ba8zb18azbcfef2e73764

Contribution des neuroblastes dérivés de la zone sous ventriculaire à la régénération de la myéline dans le cerveau de souris adulte : impact des propriétés mécaniques des tissus

Falque, M. (2023) · theses.fr (ABES) · doi:10.70675/f778841bz8528z4bd0z9904za8868abb942d

Disabling Müller Glia Preserves Retinal Function After Retinal InjuryPreprint

Larbi, D., Chen, S., Gibbons, L. D., Indictor, A., Kang, S., Rief, A. M., & Wohl, S. G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.14.718211

Absence of Glial Fibrillary Acidic Protein and Vimentin Prevents Hypertrophy of Astrocytic Processes and Improves Post-Traumatic Regeneration

Wilhelmsson, U., Li, L., Pekna, M., Berthold, C.-H., Blom, S., Eliasson, C., Renner, O., Bushong, E., Ellisman, M., Morgan, T. E., et al. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0820-04.2004 · Cited by 455

Mechanically Induced Reactive Gliosis Causes ATP-Mediated Alterations in Astrocyte Stiffness

Miller, W. J., Leventhal, I., Scarsella, D., Haydon, P. G., Janmey, P. A., & Meaney, D. F. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2008.0727 · Cited by 56

Up-Regulation of Glial Fibrillary Acidic Protein in Response to Retinal Injury: Its Potential Role in Glial Remodeling and a Comparison to Vimentin Expression

Lewis, G. P., & Fisher, S. K. (2003) · International review of cytology · doi:10.1016/s0074-7696(03)30005-1 · Cited by 380

Contribution of intermediate filaments to cell stiffness, stiffening, and growth

Wang, N., & Stamenović, D. (2000) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2000.279.1.c188 · Cited by 304

Intermediate filaments regulate astrocyte motility

Lepekhin, E. A., Eliasson, C., Berthold, C., Berezin, V., Bock, E., & Pekny, M. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00595.x · Cited by 164