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Related Concept Videos

Laminins are the Adhesive Proteins of Basal Lamina00:55

Laminins are the Adhesive Proteins of Basal Lamina

Laminins are heterotrimeric proteins with high molecular mass found in the extracellular matrix. Each laminin molecule is composed of three chains, viz. alpha, beta, and gamma, coded by five, four, and three paralogous genes, respectively. Laminins are categories based on the compositions of the three chains.
In humans, the five forms of alpha chains are LAMA 1, LAMA 2, LAMA 3, LAMA 4, and LAMA 5. The four forms of beta chains are LAMB 1, LAMB 2, LAMB 3, and LAMB 4. The three forms of gamma...
Types of Intermediate Filaments01:31

Types of Intermediate Filaments

The intermediate filaments are an essential component of the cytoskeleton. Presently six types of intermediate filament have been identified. Type I and II are acidic and basic keratin proteins. Type III is of mesodermal origin and comprises four proteins: vimentin, desmin, glial fibrillary acidic protein (GFAP), and peripherin. Vimentin is commonly found in mesenchymal cells, desmin in muscle cells, GFAP in astrocytes, while peripherin is found in peripheral nervous system neurons (PNS). Type...
Disassembly of Intermediate Filaments01:35

Disassembly of Intermediate Filaments

Intermediate filaments (IFs) do not undergo spontaneous disassembly. Enzymes, kinases, and phosphatases add and remove phosphates from specific sites to regulate their disassembly. The IF concentration in the cytoplasm also regulates the disassembly. If the concentration crosses a threshold, it activates the protein kinases in the vicinity, allowing the phosphorylation of IFs.
Keratin proteins, found at the cell periphery near cell junctions, undergo a cycle of assembly and disassembly. In Type...
Mechanism of Lamellipodia Formation01:31

Mechanism of Lamellipodia Formation

Cells migrating in response to external stimuli form lamellipodia, which are thin membrane protrusions supported by a mesh of linked, branched, or unbranched actin filaments. These actin filaments interact with myosin motor proteins, creating the dynamic actomyosin complex within the cytoskeleton. Contractility, or the ability to generate contractile stress, is inherent to the actomyosin complex. It helps cells detect the stiffness of the surrounding ECM and exert contractile force for...
Type IV Collagen of Basal Lamina01:05

Type IV Collagen of Basal Lamina

Type IV collagen is a 400 nm long, network-forming collagen that acts as a barrier between the epithelial and endothelial cells. Type IV collagen  forms the backbone of the basement membrane by scaffolding with laminin, entactin, proteoglycans, and fibronectin. Apart from rendering structural support to the basement membrane, it also helps entail signaling potentials necessary for both pathological and physiological functions.
A type IV collagen molecule has six alpha chains which can exist in...
Cytoskeletal Linker Proteins - Plakins01:09

Cytoskeletal Linker Proteins - Plakins

Plakins are large proteins with binding domains for microtubules, microfilaments, intermediate filaments, and membrane-associated protein complexes at cell junctions. Plakin functions are evolutionarily conserved and are primarily involved in organizing the different components of the cytoskeleton by crosslinking them to each other and connecting them to the cell-matrix and cell adhesion complexes. They are also known to interact with signal transducers, serve as scaffolds for signaling...

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Updated: Jun 19, 2026

Detection of Nuclear Blebbing and DNA Leakage in Mammalian Cells by Immunofluorescence
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Detection of Nuclear Blebbing and DNA Leakage in Mammalian Cells by Immunofluorescence

Published on: January 17, 2025

[Research progress in A-type lamins].

Chun-Hai Gao1, Xin-Guang Liu, Zhong-Jun Zhou

  • 1Institute of Biochemistry Molecular Biology, Guangdong Medical College, Zhanjiang 524023, China.

Sheng Li Ke Xue Jin Zhan [Progress in Physiology]
|October 7, 2009
PubMed
Summary
This summary is machine-generated.

A-type lamins, encoded by LMNA, support the nuclear lamina and organize chromatin. Mutations in LMNA cause laminopathies, a group of human diseases.

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Area of Science:

  • Cell Biology
  • Molecular Biology
  • Genetics

Context:

  • A-type lamins are key structural proteins of the nuclear lamina, essential for nuclear envelope integrity and mechanical support.
  • They interact with chromatin, influencing crucial cellular processes like gene transcription and DNA replication.

Purpose:

  • This review synthesizes current knowledge on A-type lamins, focusing on their structure, modifications, assembly, and interactions.
  • It aims to elucidate the multifaceted roles of A-type lamins in cellular functions and their implications in human diseases.

Summary:

  • A-type lamins, encoded by the LMNA gene, form the nuclear lamina, providing mechanical support and regulating chromatin organization, transcription, DNA replication, and apoptosis.
  • Dysfunctional A-type lamins due to LMNA mutations lead to a spectrum of inherited disorders known as laminopathies.

Impact:

  • Understanding A-type lamin biology is crucial for deciphering the pathogenesis of laminopathies.
  • This review provides a comprehensive resource for researchers investigating nuclear structure, gene regulation, and related human diseases.