Results 21 to 30 of about 3,755 (143)

Plectin in the Central Nervous System and a Putative Role in Brain Astrocytes

open access: yesCells, 2021
Plectin, a high-molecular-mass cytolinker, is abundantly expressed in the central nervous system (CNS). Currently, a limited amount of data about plectin in the CNS prevents us from seeing the complete picture of how plectin affects the functioning of ...
Maja Potokar, Jernej Jorgačevski
doaj   +1 more source

Plectin promotes tumor formation by B16 mouse melanoma cells via regulation of Rous sarcoma oncogene activity

open access: yesBMC Cancer, 2022
Background Melanoma is a malignant tumor characterized by high proliferation and aggressive metastasis. To address the molecular mechanisms of the proto-oncogene, Rous sarcoma oncogene (Src), which is highly activated and promotes cell proliferation ...
Kana Mizuta   +10 more
doaj   +1 more source

Vimentin Intermediate Filaments: A Paradigm Shift From Static Structure to Dynamic Cytoplasmic Network [PDF]

open access: yesBioessays
Vimentin intermediate filaments form a dynamic, motile network that interacts with microfilaments and microtubules. We propose a hybrid transport model to explain vimentin filament dynamics through cytoskeletal crosstalk and organelle‐associated transport.
Renganathan B, Adam S, Gelfand V.
europepmc   +2 more sources

Plectin-Isoform-Specific Rescue of Hemidesmosomal Defects in Plectin (–/–) Keratinocytes [PDF]

open access: yesJournal of Investigative Dermatology, 2003
The various plectin isoforms are among the major crosslinking elements of the cytoskeleton. The importance of plectin in epithelia is convincingly supported by the severe skin blistering observed in plectin-deficient humans and mice. Here, we identified plectin 1a (> 500 kDa), a full length plectin variant containing the sequence encoded by the ...
Andrä, Kerstin   +7 more
openaire   +3 more sources

Z-Disk-Associated Plectin (Isoform 1d): Spatial Arrangement, Interaction Partners, and Role in Filamin C Homeostasis

open access: yesCells, 2023
Plectin, a highly versatile cytolinker protein, is crucial for myofiber integrity and function. Accordingly, mutations in the human gene (PLEC) cause several rare diseases, denoted as plectinopathies, with most of them associated with progressive muscle ...
Lilli Winter   +11 more
doaj   +1 more source

Antibody Characterization Report for Plectin

open access: yes, 2021
Head to head comparison of available commercial antibodies against Plectin by immunoblot (Western blot), immunoprecipitation and immunofluorescence.
Ayoubi, Riham   +5 more
openaire   +2 more sources

Mitochondrial Adaptation to Mechanical Stress in Cardiac Ageing and Disease. [PDF]

open access: yesAdv Sci (Weinh)
Mechanical forces shape the heart's energy factories. This review explores how mitochondria in cardiac cells sense and respond to biomechanical stress, altering their structure, positioning, and metabolism. By linking mechanical cues to mitochondrial adaptation, the article highlights pathways driving heart disease and points to new strategies for ...
Prakash A, Iskratsch T.
europepmc   +2 more sources

Muscle-Related Plectinopathies

open access: yesCells, 2021
Plectin is a giant cytoskeletal crosslinker and intermediate filament stabilizing protein. Mutations in the human plectin gene (PLEC) cause several rare diseases that are grouped under the term plectinopathies.
Michaela M. Zrelski   +2 more
doaj   +1 more source

[99mTc]Tc-Labeled Plectin-Targeting Peptide as a Novel SPECT Probe for Tumor Imaging

open access: yesPharmaceutics, 2022
Certain receptors are often overexpressed during tumor occurrence and development and closely correlate with carcinogenesis. Owing to its overexpression on the cell membrane and cytoplasm of various tumors, plectin, which is involved in tumor ...
Jiali Gong   +4 more
doaj   +1 more source

Targeted proteolysis of plectin isoform 1a accounts for hemidesmosome dysfunction in mice mimicking the dominant skin blistering disease EBS-Ogna.

open access: yesPLoS Genetics, 2011
Autosomal recessive mutations in the cytolinker protein plectin account for the multisystem disorders epidermolysis bullosa simplex (EBS) associated with muscular dystrophy (EBS-MD), pyloric atresia (EBS-PA), and congenital myasthenia (EBS-CMS).
Gernot Walko   +12 more
doaj   +1 more source

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