HISTOLOGY REVIEW
The cell and its components
Main components of the cell
The cell membrane
The cytoplasm
The nucleus
Difference btwn cytoplasm and cytosol
Cytosol is cytoplasm minus the organelles- it’s the fluid part of the cytoplasm
Cytoplasm
Organelles
Matrix called cytosol
Forms framework of the cell referred to as cytoskeleton
Has structures know as inclusions
Difference btwn organelles and inclusions
Organelles permanent structures in a cell Inclusions could be temporary, eg lipid granules
Organelles are universal cell types while inclusions are found in specific cells eg melanin will be
found in melanocytes
Organelles have their origin from the cell, while the inclusion are usually derived from the
external environment
Functions and distribution of the following organelles
Mitochondria-
energy production produced by oxidation of fatty acids, called oxidation phosphorylation
Has its own DNA
Regulate apoptosis- whether a cell dies or not
Responsible sequestration of potassium ie for removing potassium from blood to cell-
important in preventing hypoglycemia*
Found in highly active cells
RER
Has ribosomes to provide sites for protein synthesis
Glycosylation of proteins
Provides sites for storage of calcium
Assist in transport of the synthesized proteins
Found in organs producing enzymes eg, protein synthesizing cells
SER
Synthesis of steroids or lipids eg in adrenal cortex which secretes steroids like aldosterone,
also testis, oogonia
Detoxification
Stores calcium
Synthesis of phospholipids
, Modified to form sarcoplasmic reticulum which is found in skeletal muscle and responsible
for muscle contraction
Golgi apparatus
Goes hand in hand with RER
Packaging and transportation of proteins
Forms secretory vesicles
Involved in formation of lysosomes
Ribosomes are synthesized inside the nucleolus then they will go into the cytoplasm cause
this is where protein synthesis occurs then the golgi apparatus then transports them
outside the cell in secretory vesicles where they are required
Lysosomes
Intracellular digestion of foreign materials
Destroys cellular debri- the worn out part of the cell
Lack of lysomes makes you predominant to bacterial infections
Autosomes- lysosomes destroy intracellular material
Phagosomes- destroy extracellular material
Found in cells highly active in phagocystic processes
Brain-Microglial cells
Lungs-Pulmonary alveolar microphages
Liver- kupher cells
Bone- osteoclasts
Skin-langerhans cells
Connective tissue-microphages
Blood-monocytes
Lack of em(lysosomes) results to chediak higashi syndrome- defective phagocytosis
Results to recurrent bacterial syndrome
Peroxisomes
Similar to lysosomes
Double membrane but lysosomes single membrane
Detoxification of lipids
Mainly found in hepatocytes
Disorderes affecting cell organelles
Peroxisomes-zelweger’s defective activity of peroxisomes
Lysosomes- lysosomal storage disease eg gaucheur’s disease
Mitochondria- mitochondrial myopathys
Structural components and functions of cell membrane
has a phospholipid bilayer-responsible for structural integrity of cell membrane- cell membrane
framework
with protein layer in btwn- act as receptors, ion channels, pumps cause it provides sites for drug
function
fluid in the cell membrane-responsible for the dynamism of the cel membrane ie referred to
fluid mosaic(complex of phospholipids and proteins) model
The cell and its components
Main components of the cell
The cell membrane
The cytoplasm
The nucleus
Difference btwn cytoplasm and cytosol
Cytosol is cytoplasm minus the organelles- it’s the fluid part of the cytoplasm
Cytoplasm
Organelles
Matrix called cytosol
Forms framework of the cell referred to as cytoskeleton
Has structures know as inclusions
Difference btwn organelles and inclusions
Organelles permanent structures in a cell Inclusions could be temporary, eg lipid granules
Organelles are universal cell types while inclusions are found in specific cells eg melanin will be
found in melanocytes
Organelles have their origin from the cell, while the inclusion are usually derived from the
external environment
Functions and distribution of the following organelles
Mitochondria-
energy production produced by oxidation of fatty acids, called oxidation phosphorylation
Has its own DNA
Regulate apoptosis- whether a cell dies or not
Responsible sequestration of potassium ie for removing potassium from blood to cell-
important in preventing hypoglycemia*
Found in highly active cells
RER
Has ribosomes to provide sites for protein synthesis
Glycosylation of proteins
Provides sites for storage of calcium
Assist in transport of the synthesized proteins
Found in organs producing enzymes eg, protein synthesizing cells
SER
Synthesis of steroids or lipids eg in adrenal cortex which secretes steroids like aldosterone,
also testis, oogonia
Detoxification
Stores calcium
Synthesis of phospholipids
, Modified to form sarcoplasmic reticulum which is found in skeletal muscle and responsible
for muscle contraction
Golgi apparatus
Goes hand in hand with RER
Packaging and transportation of proteins
Forms secretory vesicles
Involved in formation of lysosomes
Ribosomes are synthesized inside the nucleolus then they will go into the cytoplasm cause
this is where protein synthesis occurs then the golgi apparatus then transports them
outside the cell in secretory vesicles where they are required
Lysosomes
Intracellular digestion of foreign materials
Destroys cellular debri- the worn out part of the cell
Lack of lysomes makes you predominant to bacterial infections
Autosomes- lysosomes destroy intracellular material
Phagosomes- destroy extracellular material
Found in cells highly active in phagocystic processes
Brain-Microglial cells
Lungs-Pulmonary alveolar microphages
Liver- kupher cells
Bone- osteoclasts
Skin-langerhans cells
Connective tissue-microphages
Blood-monocytes
Lack of em(lysosomes) results to chediak higashi syndrome- defective phagocytosis
Results to recurrent bacterial syndrome
Peroxisomes
Similar to lysosomes
Double membrane but lysosomes single membrane
Detoxification of lipids
Mainly found in hepatocytes
Disorderes affecting cell organelles
Peroxisomes-zelweger’s defective activity of peroxisomes
Lysosomes- lysosomal storage disease eg gaucheur’s disease
Mitochondria- mitochondrial myopathys
Structural components and functions of cell membrane
has a phospholipid bilayer-responsible for structural integrity of cell membrane- cell membrane
framework
with protein layer in btwn- act as receptors, ion channels, pumps cause it provides sites for drug
function
fluid in the cell membrane-responsible for the dynamism of the cel membrane ie referred to
fluid mosaic(complex of phospholipids and proteins) model