Download as PDF, PPTX
Uploaded byOpen.Michigan
09.15.08: Muscle Tissue
The document provides detailed information on the structure and function of different types of muscle tissue, including skeletal, cardiac, and smooth muscle. It covers the microscopic characteristics, contraction mechanisms, regenerative potential, and connective tissue organization of each muscle type. Additionally, it addresses copyright information and the guidelines for using the material within the context of educational resources.
More Related Content
![Chapt09 Holes Lecture Animation[1]](https://cdn.slidesharecdn.com/ss_thumbnails/chapt09holeslectureanimation1-091122122851-phpapp02-thumbnail.jpg?width=640&height=640&fit=bounds)
09.15.08: Muscle Tissue
- 1. Author(s): Matthew Velkey,2009 License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution – Non-Commercial – Share Alike 3.0 License: http://creativecommons.org/licenses/by-nc-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximize your ability to use, share, and adapt it. The citation key on the following slide provides information about how you may share and adapt this material. Copyright holders of content included in this material should contact [email protected] with any questions, corrections, or clarification regarding the use of content. For more information about how to cite these materials visit http://open.umich.edu/education/about/terms-of-use. Any medical information in this material is intended to inform and educate and is not a tool for self-diagnosis or a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional. Please speak to your physician if you have questions about your medical condition. Viewer discretion is advised: Some medical content is graphic and may not be suitable for all viewers.
- 2. Citation Key for more information see: http://open.umich.edu/wiki/CitationPolicy Use + Share + Adapt { Content the copyright holder, author, or law permits you to use, share and adapt. } Public Domain – Government: Works that are produced by the U.S. Government. (USC 17 § 105) Public Domain – Expired: Works that are no longer protected due to an expired copyright term. Public Domain – Self Dedicated: Works that a copyright holder has dedicated to the public domain. Creative Commons – Zero Waiver Creative Commons – Attribution License Creative Commons – Attribution Share Alike License Creative Commons – Attribution Noncommercial License Creative Commons – Attribution Noncommercial Share Alike License GNU – Free Documentation License Make Your Own Assessment { Content Open.Michigan believes can be used, shared, and adapted because it is ineligible for copyright. } Public Domain – Ineligible: Works that are ineligible for copyright protection in the U.S. (USC 17 § 102(b)) *laws in your jurisdiction may differ { Content Open.Michigan has used under a Fair Use determination. } Fair Use: Use of works that is determined to be Fair consistent with the U.S. Copyright Act. (USC 17 § 107) *laws in your jurisdiction may differ Our determination DOES NOT mean that all uses of this 3rd-party content are Fair Uses and we DO NOT guarantee that your use of the content is Fair. To use this content you should do your own independent analysis to determine whether or not your use will be Fair.
- 3. Muscle Tissue Matthew Velkey, Ph.D. Fall 2008
- 4. Muscle Tissue I. StriatedMuscle - regularly arranged contractile units A. Skeletal Muscle - long, cylindrical multinucleated cells with peripherally placed nuclei. Contraction is typically quick and vigorous and under voluntary control. Used for locomotion, mastication, and phonation. B. Cardiac Muscle - elongated, branched cells with a single centrally placed nucleus and intercalated discs at the ends. Contraction is involuntary, vigorous, and rhythmic. II. Smooth Muscle - possesses contractile machinery, but it is irregularly arranged (thus, non-striated). Cells are fusiform with a central nucleus. Contraction is involuntary, slow, and long lasting.
- 5. Skeletal Muscle Investments Epimysium- dense irr. c.t. Perimysium - less dense irr. c.t. Endomysium - basal lamina and reticular fibers National Cancer Institute, Wikipedia ALL MUSCLE CELLS HAVE BASAL LAMINAE!
- 6. Skeletal Muscle asseen in longitudinal section in the light microscope... • Multi-nucleated and striated • A bands - anisotropic (birefringent in polarized light) • I bands - isotropic (do not alter polarized light) • Z lines (Zwischenscheiben, Ger. “between the discs”) • H zone (hell, Ger. “clear”) Gartner and Hiatt. Color Atlas of Histology. Figure 1.
- 7. Skeletal Muscle asseen in transverse section in the light microscope... Figure 2 from Plate 18. Ross and Pawlina Figure 3 from Plate 18. Ross and Pawlina
- 8. Organization of Skeletal Muscle Fibers THE SARCOMERE… Contractile unit of striated muscle • Structures between Z lines • 2 halves of I bands • A band • H zone • M line (Mittelscheibe, Ger. “middle of the disc”) • Myofilaments • Actin • Myosin • Other structural proteins • Titin (myosin-associated) • Nebulin (actin-associated) Sameerb, Wikipedia • Myomesin (at M line) • α actinin (at Z line) • Desmin (Z line) • Vimentin (Z line) • Dystrophin (cell membrane)
- 9. Transverse Section ofSkeletal Muscle: TEM view • H zone: thick filaments only – At M-line: thick filaments and myomesin lattice • A band: thick & thin filaments • I Band: thin filaments only I H M A Figure 10-11 from Junquiera. Junquiera. Figure 10-12.
- 10. Longitudinal Section ofSkeletal Muscle as observed in the TEM I Band - Actin only A Band - Actin and Myosin H Zone - Myosin only S.R./T-tubule “triad” () mitochondria Sarcoplasmic reticulum Sarc. ret. T-tubule Junquiera. Figure 10-16.
- 11. T-tubule System: Propagation ofthe Signal and Release of Ca2+ T (transverse) Tubules • run perpendicular (transversely) to myofibrils • conduct membrane depolarization deep into fibers Image of T-tubule system removed Sarcoplasmic Reticulum • smooth ER • site of Ca2+ storage & release • terminal cisternae abut T-tubules forming triads when myofibrils are viewed in longitudinal section
- 12. Longitudinal section ofmuscle showing triads • 1 T tubule • 2 terminal cisternae of sarcoplasmic reticulum • Normally at A/I junctions in mammals (this sample is from an amphibian) Junquiera. Figure 10-10.
- 13. Neuromuscular Junction Synapse: • Action potential (AP) stimulates release of acetylcholine from axon terminal into synaptic cleft • Acetylcholine in synaptic cleft binds Na+ channel receptors –initiates sarcolemma AP Signal Propagation: T (transverse) Tubules • Run perpendicular (transversely) to myofibrils • Conduct membrane depolarization deep into fibers Intracellular Ca2+ release: Sarcoplasmic Reticulum • Smooth ER, site of Ca2+ storage • Voltage-gated channels in SR detect membrane depolarization in T-tubule and release Ca2+ Source Undetermined
- 14. Muscle Innervation: Motor End Plate Source Undetermined Dake, Wikipedia 1. presynaptic terminal 2. sarcolemma 3. synaptic vesicles 4. Acetylcholine receptors 5. mitchondrion
- 15. Ca2+ Stimulates Myosin-ActinBinding and Initiates Contraction • Myosin-actin binding inhibited by TnI • TnC binds Ca2+ (if present) and induces release of TnI from actin • Myosin binds actin; hydrolysis of ATP induces power stroke • Actin filaments move relative to myosin Top left from Ross and Pawlina. Figure 11.7. Bottom left and right. Figures 10-13 and 10-14 (right). Junquiera.
- 16. Contraction Cycle 2 3 1 4 Alberts. Molecular Biology of the Cell. 1. ATP binds myosin – myosin releases actin 2. ATP hydrolysis induces conformational change – myosin head cocks forward 5nm (ADP+Pi remain bound to myosin). 3. Myosin binds weakly to actin, causing release of Pi 4. Release of Pi induces strong binding, power stroke, and release of ADP Myosin remains bound to actin if no more ATP is available (rigor conformation)
- 17. Sliding Filament Theory Sarcomere Source Undetermined Muscle fibers are composed of many contractile units (sarcomeres) Changes in the amount of overlap between thick and thin filaments allows for contraction and relaxation of muscle fibers Many fibers contracting together result in gross movement Note: Z lines move closer together; I band and H band become smaller during contraction Source Undetermined
- 18. Cardiac Muscle Tissue Features: • Striated (same contractile machinery) • Self-excitatory and electrically coupled • Rate of contractions modulated by autonomic nervous system – innervation is neuroendocrine in nature (i.e. no “motor end plates”) Cell Features: • 1 or 2 centrally placed nuclei • Branched fibers with intercalated discs • Numerous mitochondria (up to 40% of cell volume) • Sarcoplasmic reticulum & T-tubules appear as diads at Z lines – Sarcoplasmic reticulum does not form terminal cisternae – T tubules are about 2x larger in diameter than in skeletal muscle • transport Ca2+ into fibers
- 19. Cardiac Muscle (longitudinalsection) Source Undetermined
- 20. Cardiac Muscle (longitudinalsection) Cardiac Muscle (transverse section) Gartner and Hiatt. Color Atlas of Histology. Figure 2 and Figure 4 from Plate 6.8
- 21. Transverse Section ofCardiac Muscle versus Skeletal Muscle Ross and Pawlina Figure 3 from Plate 18 on right. Left U-M Histology Collection
- 22. Cardiac Muscle (TEM) T Tubule/SR Diads Left from Junquiera. Figure 10-24. Right: Source Undetermined
- 23. Intercalated Discs CoupleHeart Muscle Mechanically and Electrically Junquiera. Figure 10-25.
- 24. aka “Fascia adherens” Transverseportion: forms mechanical coupling Junquiera. Figure 10-26 Source Undetermined Lateral Portion: forms electrical coupling Cross and Mercer. Cells and Tissue Ultrastructure. 1993. Plate 120
- 25. Smooth Muscle • Fusiform,non-striated cells • Single, centrally-placed nucleus • Contraction is non-voluntary • Contraction is modulated in a neuroendocrine manner • Found in blood vessels, GI and urogenital organ walls, dermis of skin Junquiera. Figure 10-1.
- 26. Smooth Muscle (longitudinalsection) Gartner and Hiatt. Color Atlas of Histology. Figure 1 from plate 6.6 on left. Figure 2 from plate 6.6.
- 27. Smooth Muscle Viewedin Transverse and Longitudinal Section Color Atlas by Gartner and Hiatt. Figure 4 from plate 6.6. Junquiera. Figure 10-30.
- 28. Ultrastructure of SmoothMuscle: • actin and myosin filaments • intermediate filaments of desmin (also vimentin in vascular smooth muscle) • membrane associated and cytoplasmic dense bodies containing α actinin (similar to Z lines) • relatively active nucleus (smooth muscle cells make collagen, elastin, and proteoglycans) May, Naftel, and Ard. University of Mississippi Digital EM Atlas. Plate 17A.
- 29. Smooth Muscle Viewed in Cross Section (TEM) What is the structure marked by * ? Also, note collagen – SMC secrete ECM: * collagen (I,III, IV), elastin, and proteoglycans May, Naftel, and Ard. University of Mississippi Digital EM Atlas. Plate 17B
- 30. More Ultrastructure ofSmooth Muscle Cells: • microtubules (curved arrows) • dense bodies (desmin/vimentin plaques) • actin filament (arrowheads) • caveoli (membrane invaginations & vesicular • intermediate filaments system contiguous with SER –functionally analogous to sarcoplasmic reticulum) Cross and Mercer. Inset of plate 114.
- 31. Smooth Muscle Contraction: also Ca+ dependent, but mechanism is different than striated muscle 1. Ca2+ ions released from caveloae/SER and complex with calmodulin 2. Ca2+-calmodulin activates myosin light chain kinase 3. MLCK phosphorylates myosin light chain 4. Myosin unfolds & binds actin; ATP-dependent contraction cycle ensues. 5. Contraction continues as long as myosin is phosphorylated. 6. “Latch” state: myosin head attached to actin dephosphorylated causing decrease in ATPase activity –myosin head unable to detach from actin (similar to “rigor mortis” in skeletal muscle). Triggered by: • Voltage-gated Ca+ channels activated by depolarization • Mechanical stimuli • Neural stimulation • Ligand-gated Ca+ channels Ross and Pawlina. Figure 11.23.
- 32. Mechanics of Smooth Muscle Contraction • Dense bodies are analogous to Z lines (plaques into which actin filaments insert) • Myosin heads oriented in “side polar” arrangement • Contraction pulls dense Image of smooth bodies together muscle cell contraction removed Additional notes: • Contraction cycle generally about ~10% as fast as skeletal muscle • Visceral (unitary) smooth muscle cells may be electrically coupled via gap junctions and exhibit either rhythmic or tonic contraction –innervation generally MODIFIES smooth muscle activity rather than initiating it. • Multiunit smooth muscle cells are innervated individually and can contract rapidly for more precise control. • Innervation is always at a distance (no motor end plates)
- 33. Smooth Muscle (vascular) SourceUndetermined Source Undetermined Relaxed Contracted
- 34. Smooth Muscle VERSUS Color Atlas of Histology. Figure 1 from plate 8.2. Nerve Color Atlas of Histology. Figure 3 from plate 6.6 VERSUS Connective Tissue Color Atlas of Histology. Figure 1 from plate 7.5 Color Atlas of Histology. Figure 3 from plate 7.5
- 35. Epithelium Slide 250 vagina B.V. B.V. CT SM CT Nerve CT SM SM U-M Histology Collection slide 250.
- 36. 10-100µm in diameter Up to 30cm in length 10-15µm in diameter 80-100µm in length 0.2-2µm in diameter 20-200µm in length Junquiera. Figure 10-1.
- 37. Skeletal Muscle Cardiac Muscle Smooth Muscle Left: Ross and Pawlina. Figure 2 from plate 18. Middle: Unknown Right: Unknown
- 38. Muscle Regeneration andGrowth Skeletal Muscle • Increase in size (hypertrophy) • Increase in number (regeneration/proliferation) • Satellite cells are proposed source of regenerative cells Smooth Muscle • Increase in size (hypertrophy) • Increase in number (regeneration/proliferation) • Smooth muscle cells are proliferative (e.g. uterine myometrium and vascular smooth muscle) • Vascular pericytes can also provide source of smooth muscle Heart Muscle • Increase in size (hypertrophy) • Formerly thought to be non-proliferative • Post-infarction tissue remodeling by fibroblasts (fibrosis/scarring) • New evidence suggests mitotic cardiomyocytes and regeneration by blood or vascular-derived stem cells
- 39. Skeletal Muscle SatelliteCell Source Undetermined
- 40. Activated satellite cellin skeletal muscle Source Undetermined
- 41. Learning Objectives 1. Beable to identify the three types of muscle at the light and electron microscope levels, including distinctive features of each, such as the intercalated disk of cardiac muscle. 2. Be able to describe the structural basis of muscle striation. 3. Know the structural elements that harness muscle contraction (i.e., the shortening of myofibrils) to the movement of a body part (i.e., via connection to bone) as well as the mechanism by which muscle cells contract. 4. Understand the function and organization of the connective tissue in muscle (endo-, peri-, and epiysium). 5. Be familiar with the regenerative potential of each muscle type.
- 42. Additional Source Information for more information see: http://open.umich.edu/wiki/CitationPolicy Slide 5: National Cancer Institute, Wikimedia, http://en.wikipedia.org/wiki/File:Illu_muscle_structure.jpg Slide 6: Source Undetermined Slide 7: Source Undetermined Slide 8: Sameerb, Wikipedia, http://en.wikipedia.org/wiki/File:Sarcomere.gif Slide 9: Source Undetermined Slide 10: Source Undetermined Slide 12: Source Undetermined Slide 13: Source Undetermined Slide 14: Source Undetermined; Dake, Wikipedia, http://en.wikipedia.org/wiki/File:Synapse_diag4.png#file Slide 15: Source Undetermined Slide 16: Source Undetermined Slide 17: Source Undetermined Slide 19: Source Undetermined Slide 20: Source Undetermined Slide 21: Source Undetermined Slide 22: Source Undetermined Slide 23: Source Undetermined Slide 24: Source Undetermined Slide 25: Source Undetermined Slide 26: Source Undetermined Slide 27: Source Undetermined Slide 28: Source Undetermined Slide 29: Source Undetermined Slide 30: Source Undetermined Slide 31: Source Undetermined Slide 33: Source Undetermined Slide 34: Source Undetermined Slide 35: Source Undetermined Slide 36: Source Undetermined Slide 37: Source Undetermined Slide 39: Source Undetermined Slide 40: Source Undetermined