Sacroplasmic reticulum: Difference between revisions

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The Sarcoplasmic Reticulum (SR) is present in all types of muscle cell (cardiac, smooth and skeletal) and is a form of modified [[Endoplasmic_Reticulum|endoplasmic reticulum]].<ref name="null">D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 408</ref>&nbsp;It contains an essential store of Ca2+ ions; when the SR is stimulated these ions are released to initiate a contration in the muscle. In other words, the sarcoplasmic reticulum regulates the intracellular concentration of calcium ions.<ref>B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 234.</ref>  
The Sarcoplasmic Reticulum (SR) is present in all types of [[muscle|muscle]] cell (cardiac, smooth and skeletal) and is a form of modified [[Endoplasmic Reticulum|endoplasmic reticulum]]&nbsp;<ref name="null">D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 408</ref>.&nbsp;It contains an essential store of [[Calcium|Ca<sup>2+</sup>]] ions; when the SR is stimulated these ions are released to initiate a contration in the [[muscle|muscle]]. In other words, the sarcoplasmic reticulum regulates the intracellular concentration of calcium ions&nbsp;<ref>B. M. Koeppen &amp;amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 234.</ref>.


In cardiac and skeletal [[Muscle|muscle]] cells the SR surrounds the [[Myofibrils|myofibril]] and release their Ca2+ ions at areas known as terminal cisternae. Terminal cisternae are the part of the sarcoplasmic reticumlum nearest [[T-tubules|T-tubules]]. Skeletal and cardiac sarcoplasmic reticulums are similar in this way; however cardiac cells SRs are undeveloped and less dense in comparisson to skeletal cells.<ref>B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 258</ref>  
In cardiac and skeletal [[Muscle|muscle]] cells the SR surrounds the [[Myofibrils|myofibril]] and release their Ca<sup>2+</sup> [[ions|ions]] at areas known as terminal cisternae. Terminal cisternae are the part of the sarcoplasmic reticumlum nearest [[T-tubules|T-tubules]]. Skeletal and cardiac sarcoplasmic reticulums are similar in this way; however cardiac cells SRs are undeveloped and less dense in comparisson to skeletal cells&nbsp;<ref>B. M. Koeppen &amp;amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 258</ref>.<br>  


<br>
Smooth muscle cells also contain a sarcoplasmic reticulum that extends throughout the cell, in contrast to the other muscle types though, smooth muscles do not contain T-tubules and instead have junctional regions of the sarcoplasmic reticulum that abut areas of the sarcolema or [[caveolae|caveolae]]&nbsp;<ref>B. M. Koeppen &amp;amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 271.</ref>. Furthermore, Ca<sup>2+</sup> ions are not only released from the SR in smooth muscle cells but also come from the extracellular fluid during musclular contraction&nbsp;<ref>D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 434.</ref>.
 
Smooth muscle cells also contain a sarcoplasmic reticulum that extends throughout the cell, in contrast to the other muscle types though, smooth muscles do not contain T-tubules and instead have junctional regions of the sarcoplasmic reticulum that abut areas of the sarcolema or caveolae.<ref>B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 271.</ref> Furthermore, Ca2+ ions are not only released from the SR in smooth muscle cells but also come from the extracellular fluid during musclular contraction.<ref>D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 434.</ref>  


== References  ==
== References  ==


<references />
<references />

Revision as of 12:55, 29 November 2011

The Sarcoplasmic Reticulum (SR) is present in all types of muscle cell (cardiac, smooth and skeletal) and is a form of modified endoplasmic reticulum [1]. It contains an essential store of Ca2+ ions; when the SR is stimulated these ions are released to initiate a contration in the muscle. In other words, the sarcoplasmic reticulum regulates the intracellular concentration of calcium ions [2].

In cardiac and skeletal muscle cells the SR surrounds the myofibril and release their Ca2+ ions at areas known as terminal cisternae. Terminal cisternae are the part of the sarcoplasmic reticumlum nearest T-tubules. Skeletal and cardiac sarcoplasmic reticulums are similar in this way; however cardiac cells SRs are undeveloped and less dense in comparisson to skeletal cells [3].

Smooth muscle cells also contain a sarcoplasmic reticulum that extends throughout the cell, in contrast to the other muscle types though, smooth muscles do not contain T-tubules and instead have junctional regions of the sarcoplasmic reticulum that abut areas of the sarcolema or caveolae [4]. Furthermore, Ca2+ ions are not only released from the SR in smooth muscle cells but also come from the extracellular fluid during musclular contraction [5].

References

  1. D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 408
  2. B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 234.
  3. B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 258
  4. B. M. Koeppen &amp;amp;amp; B. A. Stanton, 2008, Berne &amp;amp;amp; Levy Physiology, 6th Edition, Canada: Mosby Elesevier. Page 271.
  5. D.U. Silverthorn, 2010, Human Physiology An Integrated Approach, 5th Edition, Sanfrancisco, Pearson. Page 434.