Extracellular matrix

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Extracellular matrix

HMBP

HMBP

Glycolysis
Citric acid cycle
Electron transport chain and oxidative phosphorylation
Gluconeogenesis
Glycogen metabolism
Pentose phosphate pathway
Physiological changes during exercise
Amino acid metabolism
Nitrogen and urea cycle
Fatty acid synthesis
Fatty acid oxidation
Ketone body metabolism
Cholesterol metabolism
Essential fructosuria
Hereditary fructose intolerance
Galactosemia
Pyruvate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD) deficiency
Lactose intolerance
Glycogen storage disease type I
Glycogen storage disease type II (NORD)
Glycogen storage disease type III
Glycogen storage disease type IV
Glycogen storage disease type V
Leukodystrophy
Metachromatic leukodystrophy (NORD)
Krabbe disease
Gaucher disease (NORD)
Niemann-Pick disease types A and B (NORD)
Niemann-Pick disease type C
Fabry disease (NORD)
Tay-Sachs disease (NORD)
Mucopolysaccharide storage disease type 1 (Hurler syndrome) (NORD)
Mucopolysaccharide storage disease type 2 (Hunter syndrome) (NORD)
Cystinosis
Hartnup disease
Alkaptonuria
Ornithine transcarbamylase deficiency
Phenylketonuria (NORD)
Cystinuria (NORD)
Homocystinuria
Maple syrup urine disease
Abetalipoproteinemia
Familial hypercholesterolemia
Hypertriglyceridemia
Hyperlipidemia
Disorders of carbohydrate metabolism: Pathology review
Disorders of fatty acid metabolism: Pathology review
Dyslipidemias: Pathology review
Glycogen storage disorders: Pathology review
Lysosomal storage disorders: Pathology review
Disorders of amino acid metabolism: Pathology review
Cellular structure and function
Cell membrane
Selective permeability of the cell membrane
Extracellular matrix
Cell-cell junctions
Endocytosis and exocytosis
Osmosis
Resting membrane potential
Nernst equation
Cytoskeleton and intracellular motility
Cell signaling pathways
Adrenoleukodystrophy (NORD)
Zellweger spectrum disorders (NORD)
Primary ciliary dyskinesia
Alport syndrome
Ehlers-Danlos syndrome
Osteogenesis imperfecta
Marfan syndrome
Vitamin C deficiency
Peroxisomal disorders: Pathology review
Nuclear structure
DNA structure
Transcription of DNA
Translation of mRNA
Gene regulation
Epigenetics
Amino acids and protein folding
Protein structure and synthesis
Nucleotide metabolism
DNA replication
Lac operon
DNA damage and repair
Cell cycle
Mitosis and meiosis
DNA mutations
Lesch-Nyhan syndrome
Orotic aciduria
Adenosine deaminase deficiency
Xeroderma pigmentosum
Li-Fraumeni syndrome
Bloom syndrome
Fanconi anemia
McCune-Albright syndrome
Acute radiation syndrome
Purine and pyrimidine synthesis and metabolism disorders: Pathology review
Polymerase chain reaction (PCR) and reverse-transcriptase PCR (RT-PCR)
Gel electrophoresis and genetic testing
ELISA (Enzyme-linked immunosorbent assay)
Karyotyping
DNA cloning
Fluorescence in situ hybridization
Mendelian genetics and punnett squares
Hardy-Weinberg equilibrium
Inheritance patterns
Independent assortment of genes and linkage
Evolution and natural selection
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Fragile X syndrome
Huntington disease
Myotonic dystrophy
Friedreich ataxia
Turner syndrome
Klinefelter syndrome
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
Cri du chat syndrome
Williams syndrome
Alagille syndrome (NORD)
Achondroplasia
Polycystic kidney disease
Familial adenomatous polyposis
Hereditary spherocytosis
Multiple endocrine neoplasia
Neurofibromatosis
Tuberous sclerosis
von Hippel-Lindau disease
Albinism
Cystic fibrosis
Hemochromatosis
Sickle cell disease (NORD)
Alpha-thalassemia
Beta-thalassemia
Wilson disease
X-linked agammaglobulinemia
Hemophilia
Muscular dystrophy
Wiskott-Aldrich syndrome
Mitochondrial myopathy
Autosomal trisomies: Pathology review
Muscular dystrophies and mitochondrial myopathies: Pathology review
Miscellaneous genetic disorders: Pathology review

Transcript

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Cells live within an environment called the extracellular matrix, and it’s a bit like how homes have yards and streets that surround them.

Also, just like how lots of homes form a community, lots of cells form a tissue.

And there are different types of tissues - epithelial, connective, muscular, and nervous tissue.

Each tissue has an extracellular matrix that’s got a unique composition that’s adapted for each tissue’s unique needs.

Having said that, all of the different types of extracellular matrix are made up of three major molecules - adhesive proteins, structural proteins, and proteoglycans.

First, there’s adhesive proteins, which help to stick the individual cells together and organizes the tissue into a neat structure.

Now, adhesive proteins - like integrins and cadherins - are found on the cell’s surface and they’re like molecular velcro.

Cells use adhesive proteins to anchor themselves to other cells and to molecules in the extracellular matrix.

Adhesive proteins also help communicate messages from the extracellular matrix to the cell.

For example, signals relayed by integrins can help a cell decide when it’s time to grow, divide, differentiate, or even die - like in apoptosis.

Next, there are structural proteins which give our tissues their tensile and compressive strength.

Some examples are collagens, elastins, and keratins.

Collagen is the most common type of structural protein in the human body, mostly because it resists tension and it can also stretch.

When collagen is made and released into the extracellular space, it’s in the form of a precursor called procollagen.

Procollagen is a protein made up of three polypeptide strands, each coiled into a left-handed helix, and then all three are twisted together into a right-handed triple helix or "superhelix" with three loose strands at each end.

Once procollagen is in the extracellular space, it encounters a tiny band of enzymes called collagen peptidases that cleave the loose strands at both ends of the procollagen protein, turning procollagen into tropocollagen.

Once there are enough tropocollagen molecules, they bind with one another to form a stack of collagen fibrils.

Collagen fibrils are arranged in different ways depending on the tissue, and when there’s a bunch of collagen fibrils, they can join up to form a bigger tube called a collagen fiber.

The four most common types of collagen are I, II, III, and IV.

Key Takeaways

The extracellular matrix (ECM) refers to the mixture of proteins and carbohydrates that surrounds cells and provides structural and biochemical support. ECM components can be put into three categories: adhesive proteins, structural proteins, and proteoglycans.

Adhesive proteins are needed to stick individual cells together, forming an organized tissue. They include integrins and cadherins. Next, structural proteins provide the tissues with structural support, including tensile strength. These proteins include keratins, and elastin. There are also proteoglycans which fill up the space between cells, helping to trap water molecules thanks to their negative charges.

The ECM also plays an important role in the communication between cells, mediating cell-to-cell interaction and cell-matrix interaction. Dysfunction of the ECM can lead to diseases such as cancer, arthritis, and fibrosis.