Tendon Biomechanics: Difference between revisions

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== Tendon Structure, Composition, and Mechanical Properties  ==


== Tendon Structure, Composition, and Mechanical Properties ==
Tendons have a hierarchy of fibrillar arrangement that is sequentially composed of collagen molecules, fibrils, fibers, fascicles (or fiber bundles), and the tendon unit. Tendon units are surrounded by epitenon, which functions to reduce friction with adjacent tissues.


Tendons have a hierarchy of fibrillar arrangement that is sequentially composed of collagen molecules, fibrils, fibers, fascicles (or fiber bundles), and the tendon unit. Tendon units are surrounded by epitenon, which functions to reduce friction with adjacent tissues.
The key to the tendons’ tensile strength is collagen.11 Type I collagen accounts for about 70–80% of the dry weight of normal tendons. In addition to type I collagen, many other types of collagen are also present, including type III (form rapid cross-links in stabilizing repair sites in the case of tears), type V (regulates collagen fibril diameter), and type XII (provides lubrication between collagen fibers).  


The key to the tendons’ tensile strength is collagen.11 Type I collagen accounts for about 70–80% of the dry weight of normal tendons. In addition to type I collagen, many other types of collagen are also present, including type III (form rapid cross-links in stabilizing repair sites in the case of tears), type V (regulates collagen fibril diameter), and type XII (provides lubrication between collagen fibers).
In addition to collagen, many proteoglycans (e.g. aggrecan and decorin) and glycoproteins (e.g. tenascin-C, fibronectin, and elastin) also have important functions in tendons. Aggrecan holds water and resists compression, and decorin facilitates fibrillar slippage. Tenascin-C, fibronectin, and elastin function to enhance mechanical stability, facilitate tendon healing, and allow tendons to return to their prestretched lengths after physiological loading, respectively.  
 
In addition to collagen, many proteoglycans (e.g. aggrecan and decorin) and glycoproteins (e.g. tenascin-C, fibronectin, and elastin) also have important functions in tendons. Aggrecan holds water and resists compression, and decorin facilitates fibrillar slippage. Tenascin-C, fibronectin, and elastin function to enhance mechanical stability, facilitate tendon healing, and allow tendons to return to their prestretched lengths after physiological loading, respectively.


== Physiological Mechanoresponses  ==
== Physiological Mechanoresponses  ==
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== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed])  ==
== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed])  ==
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== References ==
== References ==


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Revision as of 19:33, 26 December 2015

Tendon Structure, Composition, and Mechanical Properties[edit | edit source]

Tendons have a hierarchy of fibrillar arrangement that is sequentially composed of collagen molecules, fibrils, fibers, fascicles (or fiber bundles), and the tendon unit. Tendon units are surrounded by epitenon, which functions to reduce friction with adjacent tissues.

The key to the tendons’ tensile strength is collagen.11 Type I collagen accounts for about 70–80% of the dry weight of normal tendons. In addition to type I collagen, many other types of collagen are also present, including type III (form rapid cross-links in stabilizing repair sites in the case of tears), type V (regulates collagen fibril diameter), and type XII (provides lubrication between collagen fibers).

In addition to collagen, many proteoglycans (e.g. aggrecan and decorin) and glycoproteins (e.g. tenascin-C, fibronectin, and elastin) also have important functions in tendons. Aggrecan holds water and resists compression, and decorin facilitates fibrillar slippage. Tenascin-C, fibronectin, and elastin function to enhance mechanical stability, facilitate tendon healing, and allow tendons to return to their prestretched lengths after physiological loading, respectively.

Physiological Mechanoresponses[edit | edit source]

Pathological Mechanoresponses[edit | edit source]

The Differential Effects of Mechanical Loading on Tendons[1][edit | edit source]

Mechanical Load Level Effects on Tendon

Low

• ↓ Tensile strength
• ↓ Size
• ↓ Collagen production
• ↓ Anabolic activities
• ↑ Catabolic activities

Moderate

• ↑ Tensile strength
• ↑ Collagen synthesis
• ↓ Collagen degradation
• ↓ Adhesions
• ↓ Inflammatory mediator (e.g. prostaglandin E2, PGE2)
• ↑ Tendon stem cells (TSCs) differentiating into tenocytes

Excessive

• ↓ Tensile strength
• ↓ Collagen organization
• ↑ Myofibroblasts
• ↑ Inflammatory mediators
• ↑ TSCs differentiating into nontenocytes (adipocytes, osteocytes, chondrocytes)
• ↑ Leukotrienes (↑ edema)


Recent Related Research (from Pubmed)[edit | edit source]

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References[edit | edit source]

  1. Wang JHC, Guo Q, Li B. Tendon Biomechanics and Mechanobiology - A Minireview of Basic Concepts and Recent Advancements. J Hand Ther, 2012; 25(2): 133–141.