Wednesday, December 29, 2004

ECM Basics -- Cartilage Components

Cartilage, and all of the stuff that cells dump onto their outer surfaces by secretion, is made up of proteins and polysaccharides. The polysaccharides, polymers of simple sugars, are of two types, big acidic (negatively charged) polymers (hyaluronans) and backbone proteins decorated with medium-sized acidic polysaccharides (heparin sulfate and keratan sulfate). [The acidic quality (-COOH) of the polysaccharides will become more significant later because of its ability to form ester linkages through borates.] The proteins are also of two types, huge hairy fibers of collagen and tri-headed, hydras that bind to the other polysaccharides and proteins.
Collagens make up most of the protein of the external material, the extracellular matrix. If meat, muscle tissue, is heated for a prolonged time, the connective tissue (not the actin and myosins of the muscle fibers) collagens are dissolved. If the collagen solution is cooled, the collagen molecules stick together in a disorganized way and instead of reforming thick, long fibers of hundreds of bundles of extended collagen protein molecules, a sponge of millions of cross-linked proteins is formed -- gelatin. There are about three dozen different collagen proteins, each coded by a different gene, but they are all produced according to the same basic pattern. Different cell types produce a different set of collagens and as a consequence the cells become embedded in a different extracellular matrix.
Collagen proteins are synthesized on ribosomes in the cytoplasm of most cells. As the collagen is synthesized by the addition of one amino acid at a time, the growing protein chain is pulled into the endoplasmic reticulum. The full length procollagen molecules are swept into vesicles and transported through a series of membrane structures where the ends of the proteins are cut off (the pieces removed are important) by enzymes (metaloproteinases) and amino acids along the protein are oxidized. Vitamin C is essential in the oxidation of proline to hydroxyproline, which takes place during transit through the Golgi. [Insufficient vitamin C can lead to the deficiency disease called scurvy. One of the characteristics of scurvy is disruption of connective tissue -- loose teeth, bleeding. Similarly, heart disease may be a form of chronic, subsymptomatic scurvy due to vitamin C deficiency and inadequate repair of repetitively stretched coronary arteries.] Reteated sequences of glycine, proline, hydroxyproline, along the collagen, permit the protein to twist in triplets to form the collagen units that stack up into long, thick fiber after the matrix materials are secreted onto the surface of a cell. Different collagen proteins have slightly different amino acid sequences and are modified at different rates and assemblee in different ways into the fibers. Some are clipped, modified and stacked neatly into the fiber without loose ends, while others retain their ends and limit the size of the fibers as they form a shaggy surface layer. The loose ends can bind to other molecules in the matrix. Still other collagens retain their heads and form a hydra-like or three-fold caducious structure, with a twisted gly, pro, hyp repeat shaft. The heads bind the acidic polysaccharides and other components of the matrix.
The matrix components must be made, stored, secreted, assembled into functional matrix, change conformations in response to mechanical and chemical changes in the environment and be disassembled to permit replacement. Enzymes facilitate these processes and the proteolytic enzymes involved can be activated or inactivated by metal ions, hence they are named metaloproteinases and are typically called MMPs or matrix metaloproteinases. The metals involved are Zn++, Ca++, and Mg++. To further complicate the picture, the structures of the heads of the collagens are also dependent on the binding of divalent cations. Thus, it can be expected that the activity of the MMPs as well as their substrate collagens will be altered by the ion environment of the intracellular organelles, the region immediately next to the cytoplasmic membrane outside the cell (the pericellular region) and the more distant extracellular region. The mechanical stresses applied to the extracellular matrix may change the shapes of the collagen components and alter their ion binding properties with subsequent changes in the activity of the MMPs embedded in the matrix.
Clipping off the ends of collagens by MMPs releases small peptides of 40-400 amino acids in length. Many of these peptides have sequences that are related to sequences of peptide hormones, such as the cytokines. It is possible that the processing peptides released during matrix secretion, pericellular modifications and response to environmental changes my provide signals to neighboring cells embedded in the matrix. Connective tissue diseases may result from any abnormalities in the production of signalling molecules by the matrix cells.

3 Comments:

Blogger Kris said...

Are there known specific correlations between the presence, or lack thereof, of certain metal ions in the pericellular region and increased levels of specific cytokines as a result of altered MMP activity? Or are there just too many variations to really see a pattern? Then, just as a side question...in order to test this could you run a control culture, experimental culture and then run an ELISA or something like that to quantitatively look for differences?

January 23, 2005 at 10:30 AM  
Blogger Linker said...

I don't know of any correlations, but I would think that this could be tested with chelators to remove ions from particular MMPs. There are libraries of antibodies to various cytokines, but I don't know how many of the "matrikines" that are discussed here would be covered. I suspect a couple would be covered by antibodies and the rest would be detectable by isolation and MS/MS.
Thanks for the comments. Sorry I got back to this so slowly.

February 27, 2005 at 11:59 PM  
Blogger Ilya said...

Hi, Art,
I follow your "Cooling Inflammation" Blog and I have a query I'd like to discuss but don't want to mess with the ongoing discussion there as it concerns some earlier topics and a research I've been involved in the last 6 years. Would you be so kind to e-mail me back with an e-mail where I can reach you. Thank you in advance and will be waiting to hear from you.

March 23, 2010 at 1:27 PM  

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