Website: www.kosheeka.com
Smooth Muscle Cell: Understand
Function and Anatomy
Smooth muscle cells or myocytes are ubiquitously present in the body. They
maintain vasomotor tone in the aorta, airway diameter in the lungs, and milk
ejection in the mammary gland. They can alter their physiology in accordance
with the external stimuli. However, abnormal organization or cell proliferation
is implicated in diseases such as asthma, atherosclerosis, hypertension, etc.
Several medications even target these myocytes, like bronchodilators that
relax the inflammation in airway smooth muscles. However, many of its
aspects remain in the shadows.
Smooth Muscle Cells
These are essential for various body functions. They differ from skeletal
myocytes in their involuntary control by the nervous system and contractile
ability.
Structure: They possess a fusiform shape, that is, they are thick in the middle
region and taper at the ends, along with an elongated nucleus. Actin (thin) and
myosin (thick) filaments confer the contractility to them. An array of these
Website: www.kosheeka.com
filaments is absent in smooth myocytes, thus giving a non-striated appearance,
unlike skeletal myocytes. Electron micrographs exhibit dense bodies which
contain the proteins responsible for contraction. Myocytes interact with each
other via adherents or gap junctions for a uniform contraction across the
tissue. The cell arrangement in a multi-layer structure allows optimal
contractility. However, any change in the alignment can give rise to a
pathological condition. For example, myocytes assume spheroid arrangement
in uterine fibroids.
Function and Location: Smooth Myocytes are mostly present at the walls of
hollow organs such as lungs, blood vessels, urinary tract, and gastrointestinal
systems. They are responsible for regulating the tissue tone and synthesizing
the extracellular matrix (ECM) proteins. Through these functions, they regulate
blood pressure, pupil dilation, food movement, urine flow, and bronchiole
volume. Their mechanisms of action include the increase of cytoplasmic
calcium under the influence of stimuli via two manners- calcium influx from
plasma membrane channels and calcium release from the sarcoplasmic
reticulum. Calcium binds to calmodulin and further activates myosin light chain
kinase (MLCK), which induces the contraction of actin-myosin elements.
Isolation of Smooth Muscle Cells
Enzymatic and explant methods are two ways to isolate smooth myocytes.
Both methods require the removal of connective tissue to obtain vessels. The
residual tissue is cut into smaller pieces after scraping off the endothelium
along its length.
Enzymatic Method: This method requires the addition of the solution of
collagenase and then elastase enzymes to the tissue. In a few hours, cells
appear on the flasks. Digestion of the tissue follows the centrifugation and
culturing of cells.
Explant Method: It entails placing the tissue pieces with their luminal side
towards the substrate after the removal of endothelium. After ensuring the
attachment of tissue pieces to the culture dish, more media is added gently.
After a few weeks, a sufficient density of myocytes is visible on the cell culture
Website: www.kosheeka.com
dish, allowing the removal of tissue pieces and following a normal culture
process.
Characterization: The cells can now be characterized by morphology and
markers such as α-SM actin, myosin heavy chain, desmin, SM22α, etc. The
absence of endothelial cells is noticeable by negative staining for von
Willebrand factor (vWF) and acetylated low-density lipoproteins (LDL). Since a
specific marker for these cells does not exist, the evaluation of a range of
markers provides adequate verification.
Culture of Smooth Muscle Cells
Smooth myocytes assume two distinct phenotypes- contractile and synthetic.
The synthetic phenotype has low contractility along with high proliferation,
rough endoplasmic reticulum, and ECM synthesis compared to the contractile
phenotype. Supplementation of cell culture medium with basic fibroblast
growth factor and insulin preserves the contractile phenotype. In contrast, the
culture dish requires coating with collagen type I. The synthetic phenotype
exhibits a hill and valley appearance in the culture. In the in vitro culture, the
contractile force of cells exceeds the cell-substrate interactions, leading to the
formation of a three-dimensional structure resembling a hill and valley pattern.
Primary Lung Smooth Muscle Cells: Maintaining
Respiratory Health
Smooth myocytes extend from the trachea all the way up to the bronchioles.
Their key function is to regulate the diameter of bronchioles and airway
resistance. According to the developmental model, they arise from neural crest
cells. Myocytes have been involved in the pathology of chronic lung diseases.
They participate in airway inflammation, wall thickness, and hyper-
responsiveness. Studies have suggested that inflammation drives the
upregulation of certain receptors and kinases, leading to increased cellular
sensitivity. Lung diseases also demonstrate the increased number and size of
myocytes. The increase in cell proliferation as a repair response to injury could
contribute to cell number increase. Additionally, they also drive inflammation
by expressing adhesion molecules and releasing chemokines and cytokines.
Website: www.kosheeka.com
Primary Aortic Smooth Muscle Cells: Supporting
Vascular Integrity
The smooth myocytes are the prominent cell type in the tunica media layer of
the aorta. The myocytes present in the ascending aorta and aortic arch
originate from the neural crest cells, whereas those in the descending aorta
belong to the somatic mesoderm. They provide structural and functional
support as well as respond or adapt to mechanical and environmental cues by
transitioning between contractile and synthetic phenotypes. Factors like
inflammation, oxidative stress, injury, etc., can trigger the apoptosis of these
myocytes. It also impairs the ability to repair and regenerate ECM, which
confers elasticity to the aorta. Additionally, it also causes a shift into synthetic
phenotype and the secretion of ECM-degrading proteolytic enzymes. The
degraded matrix promotes the migration of myocytes, leading to apoptosis.
Any dysfunction can weaken the aortic wall, causing dilatation and resulting in
aortic aneurysms.
Human Mammary Smooth Muscle Cells: Role in
Breast Cancer
Myoepithelial cells are specialized smooth myocytes or muscle cells of the
mammary gland. Its contractile feature aids in milk ejection during lactation.
They also contribute to the mammary gland remodeling. Moreover, studies
have suggested their role in tissue polarity and enhancing cell survival. In
response to oxytocin, they contract via actin-myosin proteins and calcium-
dependent pathways. Dysregulation of human mammary smooth muscle cells
causes breast cancer progression. Breast carcinoma demonstrates changes in
tissue polarity, loss of myoepithelial cells, and structural collapse of the tissue.
The expression of ECM proteins, angiogenesis inhibitors, and ECM
accumulation by these cells might contribute to the non-invasiveness of breast
cancer. Thus, myoepithelial cells could be the key to breast carcinoma
treatment.
Website: www.kosheeka.com
The Final Outlook
The rising mortality due to lung disease, cardiovascular disorders, and breast
cancer has prompted the discovery of an absolute cure. Smooth myocytes or
muscle cells have emerged as a therapeutic target for drug development. They
play a pivotal role in the structure and function of a tissue. Their dysfunction
has been associated with several diseases. The research continues to
understand the signaling pathways of myocytes in normal and diseased tissues.
Kosheeka provides smooth myocytes or muscle cells to accelerate your
research and drug discovery process. Their team of expert scientists ensures
the quality of the product by following GMP-compliant protocols and
performing high-throughput screening to promote hassle-free research.
FAQs:
Q: What are smooth myocytes or muscle cells?
They are spindle-shaped cells containing contractile proteins actin and myosin.
Their key function is to maintain the tone of the tissue and synthesize the
extracellular matrix, thus supporting the structure and function of the tissue.
Q: What are the different phenotypes of smooth myocytes?
They have two phenotypes- contractile and synthetic. As compared to the
contractile phenotype, the synthetic phenotype is less contractile but has a
higher proliferation rate and rough endoplasmic reticulum, along with
increased ECM synthesis.
Q: What is hill and valley morphology?
Synthetic smooth myocytes often form a three-dimensional structure in the
cell culture, which resembles a hill and valley, thus giving the same name to
the growth pattern.
Q: What disorder or diseases are smooth myocytes implicated in?
They are involved with asthma, atherosclerosis, aortic aneurysms, breast
cancer, etc.

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Smooth Muscle Cell: Understand Function and Anatomy

  • 1. Website: www.kosheeka.com Smooth Muscle Cell: Understand Function and Anatomy Smooth muscle cells or myocytes are ubiquitously present in the body. They maintain vasomotor tone in the aorta, airway diameter in the lungs, and milk ejection in the mammary gland. They can alter their physiology in accordance with the external stimuli. However, abnormal organization or cell proliferation is implicated in diseases such as asthma, atherosclerosis, hypertension, etc. Several medications even target these myocytes, like bronchodilators that relax the inflammation in airway smooth muscles. However, many of its aspects remain in the shadows. Smooth Muscle Cells These are essential for various body functions. They differ from skeletal myocytes in their involuntary control by the nervous system and contractile ability. Structure: They possess a fusiform shape, that is, they are thick in the middle region and taper at the ends, along with an elongated nucleus. Actin (thin) and myosin (thick) filaments confer the contractility to them. An array of these
  • 2. Website: www.kosheeka.com filaments is absent in smooth myocytes, thus giving a non-striated appearance, unlike skeletal myocytes. Electron micrographs exhibit dense bodies which contain the proteins responsible for contraction. Myocytes interact with each other via adherents or gap junctions for a uniform contraction across the tissue. The cell arrangement in a multi-layer structure allows optimal contractility. However, any change in the alignment can give rise to a pathological condition. For example, myocytes assume spheroid arrangement in uterine fibroids. Function and Location: Smooth Myocytes are mostly present at the walls of hollow organs such as lungs, blood vessels, urinary tract, and gastrointestinal systems. They are responsible for regulating the tissue tone and synthesizing the extracellular matrix (ECM) proteins. Through these functions, they regulate blood pressure, pupil dilation, food movement, urine flow, and bronchiole volume. Their mechanisms of action include the increase of cytoplasmic calcium under the influence of stimuli via two manners- calcium influx from plasma membrane channels and calcium release from the sarcoplasmic reticulum. Calcium binds to calmodulin and further activates myosin light chain kinase (MLCK), which induces the contraction of actin-myosin elements. Isolation of Smooth Muscle Cells Enzymatic and explant methods are two ways to isolate smooth myocytes. Both methods require the removal of connective tissue to obtain vessels. The residual tissue is cut into smaller pieces after scraping off the endothelium along its length. Enzymatic Method: This method requires the addition of the solution of collagenase and then elastase enzymes to the tissue. In a few hours, cells appear on the flasks. Digestion of the tissue follows the centrifugation and culturing of cells. Explant Method: It entails placing the tissue pieces with their luminal side towards the substrate after the removal of endothelium. After ensuring the attachment of tissue pieces to the culture dish, more media is added gently. After a few weeks, a sufficient density of myocytes is visible on the cell culture
  • 3. Website: www.kosheeka.com dish, allowing the removal of tissue pieces and following a normal culture process. Characterization: The cells can now be characterized by morphology and markers such as α-SM actin, myosin heavy chain, desmin, SM22α, etc. The absence of endothelial cells is noticeable by negative staining for von Willebrand factor (vWF) and acetylated low-density lipoproteins (LDL). Since a specific marker for these cells does not exist, the evaluation of a range of markers provides adequate verification. Culture of Smooth Muscle Cells Smooth myocytes assume two distinct phenotypes- contractile and synthetic. The synthetic phenotype has low contractility along with high proliferation, rough endoplasmic reticulum, and ECM synthesis compared to the contractile phenotype. Supplementation of cell culture medium with basic fibroblast growth factor and insulin preserves the contractile phenotype. In contrast, the culture dish requires coating with collagen type I. The synthetic phenotype exhibits a hill and valley appearance in the culture. In the in vitro culture, the contractile force of cells exceeds the cell-substrate interactions, leading to the formation of a three-dimensional structure resembling a hill and valley pattern. Primary Lung Smooth Muscle Cells: Maintaining Respiratory Health Smooth myocytes extend from the trachea all the way up to the bronchioles. Their key function is to regulate the diameter of bronchioles and airway resistance. According to the developmental model, they arise from neural crest cells. Myocytes have been involved in the pathology of chronic lung diseases. They participate in airway inflammation, wall thickness, and hyper- responsiveness. Studies have suggested that inflammation drives the upregulation of certain receptors and kinases, leading to increased cellular sensitivity. Lung diseases also demonstrate the increased number and size of myocytes. The increase in cell proliferation as a repair response to injury could contribute to cell number increase. Additionally, they also drive inflammation by expressing adhesion molecules and releasing chemokines and cytokines.
  • 4. Website: www.kosheeka.com Primary Aortic Smooth Muscle Cells: Supporting Vascular Integrity The smooth myocytes are the prominent cell type in the tunica media layer of the aorta. The myocytes present in the ascending aorta and aortic arch originate from the neural crest cells, whereas those in the descending aorta belong to the somatic mesoderm. They provide structural and functional support as well as respond or adapt to mechanical and environmental cues by transitioning between contractile and synthetic phenotypes. Factors like inflammation, oxidative stress, injury, etc., can trigger the apoptosis of these myocytes. It also impairs the ability to repair and regenerate ECM, which confers elasticity to the aorta. Additionally, it also causes a shift into synthetic phenotype and the secretion of ECM-degrading proteolytic enzymes. The degraded matrix promotes the migration of myocytes, leading to apoptosis. Any dysfunction can weaken the aortic wall, causing dilatation and resulting in aortic aneurysms. Human Mammary Smooth Muscle Cells: Role in Breast Cancer Myoepithelial cells are specialized smooth myocytes or muscle cells of the mammary gland. Its contractile feature aids in milk ejection during lactation. They also contribute to the mammary gland remodeling. Moreover, studies have suggested their role in tissue polarity and enhancing cell survival. In response to oxytocin, they contract via actin-myosin proteins and calcium- dependent pathways. Dysregulation of human mammary smooth muscle cells causes breast cancer progression. Breast carcinoma demonstrates changes in tissue polarity, loss of myoepithelial cells, and structural collapse of the tissue. The expression of ECM proteins, angiogenesis inhibitors, and ECM accumulation by these cells might contribute to the non-invasiveness of breast cancer. Thus, myoepithelial cells could be the key to breast carcinoma treatment.
  • 5. Website: www.kosheeka.com The Final Outlook The rising mortality due to lung disease, cardiovascular disorders, and breast cancer has prompted the discovery of an absolute cure. Smooth myocytes or muscle cells have emerged as a therapeutic target for drug development. They play a pivotal role in the structure and function of a tissue. Their dysfunction has been associated with several diseases. The research continues to understand the signaling pathways of myocytes in normal and diseased tissues. Kosheeka provides smooth myocytes or muscle cells to accelerate your research and drug discovery process. Their team of expert scientists ensures the quality of the product by following GMP-compliant protocols and performing high-throughput screening to promote hassle-free research. FAQs: Q: What are smooth myocytes or muscle cells? They are spindle-shaped cells containing contractile proteins actin and myosin. Their key function is to maintain the tone of the tissue and synthesize the extracellular matrix, thus supporting the structure and function of the tissue. Q: What are the different phenotypes of smooth myocytes? They have two phenotypes- contractile and synthetic. As compared to the contractile phenotype, the synthetic phenotype is less contractile but has a higher proliferation rate and rough endoplasmic reticulum, along with increased ECM synthesis. Q: What is hill and valley morphology? Synthetic smooth myocytes often form a three-dimensional structure in the cell culture, which resembles a hill and valley, thus giving the same name to the growth pattern. Q: What disorder or diseases are smooth myocytes implicated in? They are involved with asthma, atherosclerosis, aortic aneurysms, breast cancer, etc.