- College 2024ุงูู ูู ุงููู ุงูุฏูุชูุฑ ุดุฑุญ ู ูู ูู ุงูู ุญุงุถุฑุฉ
- Dr . Fatma 2026
- Dr. Sherin Hamedููุช ุฃูู ุ ุดุฑุท ู ุจุณุท
- Dr. Iman Nabilููุช ุฃุทูู ุ ููู ุจูุณุจุฉ ุฃุนูู ุ ุจุงุณุชูุงุถุฉ ูู ุงูุดุฑุญ
- Dr. Moaaz Wahdanุฏูุชูุฑ ุฒู ูููุง ุ ุงูุดุฑุญ ุนูู ู ููุฌ ุงููููุฉ
- ู ูุฎุตููุฏุฑ ูุฐุงูุฑ ู ูู ุจุณ ุงูุงุนุชู ุงุฏ ุงูุฃุณุงุณู ุนูู ู ูู ุงูุฏูุชูุฑ ุฃู ูุชุงุจ ุงููุณู
- Quize
๐ I. Endoplasmic Reticulum (ER)
๐ Definition
- A membrane network within cytoplasm.
โEndoโ = inside, โplasmicโ = cytoplasm, โreticulumโ = network.
๐ Classification & Structure
- Two types:
- Smooth Endoplasmic Reticulum (SER)
โ smooth surface. - Rough Endoplasmic Reticulum (RER)
โ rough surface due to ribosomes attached.
โ Continuous tubes/sacs connected together.
โ Continuous with nuclear membrane.
- Smooth Endoplasmic Reticulum (SER)
๐ Nature
- Classified as a membranous organelle.
- Structure: delicate tubules / cisternae (histological term).
๐ Distribution & Appearance
Present in all cells.
1. RER
- Abundant in cells specialized in protein synthesis.
- (Exam Point) โRough = Protein.โ
Light Microscopy (LM):
- Not directly visible.
- If abundant โ cytoplasm appears basophilic (blue) due to RNA in ribosomes binding basic dyes (H&E).
Electron Microscopy (EM):
- Appears as connected tubules/sacs with rough outer surface (ribosomes = dark electron-dense granules).
2. SER
- Abundant in cells with lipid/fat metabolism.
- LM: not visible.
- EM: network of smooth-surfaced tubules.
๐ Functions of ER
1. RER โ Protein Synthesis & Modification
- Step 1: Translation occurs at ribosomes using mRNA from nucleus.
- Step 2: Ribosomes attach to RER; new proteins enter RER tubules.
- Step 3: Proteins undergo initial modification (defects โ hereditary diseases).
- Step 4: Modified protein + RER membrane pinch off โ vesicle.
- Step 5: Vesicle moves to Golgi apparatus for further processing.
(Note: Proteins form structural, enzymatic, and hormonal elements except steroid hormones.)
2. SER โ Lipid & Detoxification Functions
- (Exam Point) Synthesis of lipids, phospholipids, and steroid hormones.
- (Exam Point) Detoxification of toxins & drugs (mainly in liver).
- (Exam Point) Calcium storage in muscle cells for contraction.
๐ II. Mitochondria
๐ Definition
- Known as the Powerhouse of the Cell.
๐ Distribution & Size
- Present in all cells except:
- Red Blood Cells (RBCs)
- Terminal Keratinocytes
- (Exam Point) Size not required for memorization.
๐ Appearance (Light Microscopy)
- Not visible with routine H&E.
- Seen only with special stains (Exam Point):
- Iron Hematoxylin
- Janus Green
- Acid Fuchsin
- Appear as rods or spheres.
๐ Appearance (Electron Microscopy)
- Surrounded by two membranes (double unit membranes).
1. Outer Mitochondrial Membrane (OMM):
- Smooth, permeable.
2. Inner Mitochondrial Membrane (IMM):
- Folded inward โ Cristae (shelf-like structures).
- Selectively permeable.
- Contains Cardiolipin โ responsible for selective permeability.
3. Intermembrane Space:
- Between OMM & IMM.
- Contains Hโบ ions for respiratory chain reactions.
4. Mitochondrial Matrix:
- Fluid inside IMM.
- IMM folds (cristae) โ increase surface area. (Exam Point)
5. F1 Particles (Elementary Particles):
- On IMM surface facing matrix.
- Tennis racket appearance. (Exam Point)
- Contain enzymes for ATP synthesis.
๐ Mitochondrial DNA & Division
- Contains its own DNA โ can divide independently (non-synchronous).
- Mitochondrial DNA:
- Circular shape, in matrix.
- 1% of total cell DNA.
- Nuclear DNA:
- Double helix, in nucleus.
- 99% of total DNA.
๐ Types (EM Classification)
- Orthodox Type: clear cristae & matrix โ resting cells.
- Condensed Type: dense cristae, indistinct matrix โ active cells.
๐ III. Golgi Apparatus (GA)
๐ Definition
- Membranous organelle responsible for secretion. (Exam Point)
๐ Distribution & Location
- Present in all cells.
- Prominent in secretory cells.
๐ Appearance (Light Microscopy)
- Not seen with routine H&E.
- Negative Golgi Image (Exam Point):
- Seen as clear unstained area near nucleus in highly basophilic cells (e.g. plasma cells).
- Special Stains: Silver โ brown filaments (Fittaniya).
๐ Appearance (Electron Microscopy)
- Series of flattened sacs (cisternae/saccules) stacked like plates.
- Two faces:
- Cis / Forming / Convex Face: faces RER & nucleus.
- Trans / Mature / Concave Face: faces cell membrane โ site of secretion.
๐ Functions
- Post-translational modification & packaging of proteins from RER.
- Modification:
- Glycosylation โ glycoproteins.
- Trimming of protein chains.
- Secretion:
- Final vesicles pinch off from Trans face.
- Membrane recycling: forms membranes of RER & cell membrane.
- Lysosome formation: produces lysosomal enzymes.
๐ IV. Lysosomes
๐ Definition
- Digestive system of the cell.
๐ Contents & Origin
- Contain hydrolytic enzymes (digestive enzymes).
- Enzymes synthesized in RER, packaged by Golgi apparatus.
๐ Appearance
- LM: not visible normally.
- EM: membrane-bound vesicles with enzyme content.
๐ Classification (Functional State)
- Primary Lysosome:
- Newly formed, inactive, from Golgi.
- Has not yet fused with target.
- Secondary Lysosome:
- Formed after fusion with a target vesicle.
- Subtypes:
- Phagolysosome: fusion with Phagosome (solid material).
- Multivesicular Body: fusion with Pinocytic vesicle (fluid).
- Autophagic Vacuole: digestion of cellโs own organelles (self-eating).
- Residual Body (Exam Point):
Lipofuscin Pigment (Exam Point): - Indigestible waste left after digestion.
- Normally expelled.
- Accumulates in nerve cells & cardiac muscle cells (non-dividing).
- Represents undigested residual bodies.
๐ Functions
- Digestion & elimination of harmful substances (internal/external).
- Cell metabolism: activates thyroid hormone.
- Post-mortem autolysis:
- After death, lysosomal membranes rupture โ enzymes digest cell โ decomposition.
๐จ Clinical Note
- Lysosomal Storage Diseases: genetic defects in lysosomal enzymes โ substrate accumulation.
- Example: Gaucherโs Disease โ deficiency of Glucocerebrosidase โ buildup of Glucocerebroside in tissues (muscle, brain, joints).
๐ V. Peroxisomes
๐ Definition
- Structurally resemble lysosomes but contain oxidative enzymes.
๐ Contents & Functions
- (Exam Point) Contain oxidative enzymes (vs. lysosomal hydrolytic enzymes).
- Functions:
- Fatty acid oxidation.
- Alcohol detoxification.
- Use oxidative enzymes for metabolism.
๐ Origin
- (Exam Point) Not derived from Golgi apparatus.
๐ Structure (EM)
- Membrane-bound vesicles.
- May appear as coated vesicles (protection from digestion).
๐ I. Endoplasmic Reticulum (ER)
๐ Definition
- A membrane network within cytoplasm.
โEndoโ = inside, โplasmicโ = cytoplasm, โreticulumโ = network.
๐ Classification & Structure
- Two types:
- Smooth Endoplasmic Reticulum (SER)
โ smooth surface. - Rough Endoplasmic Reticulum (RER)
โ rough surface due to ribosomes attached.
โ Continuous tubes/sacs connected together.
โ Continuous with nuclear membrane.
- Smooth Endoplasmic Reticulum (SER)
๐ Nature
- Classified as a membranous organelle.
- Structure: delicate tubules / cisternae (histological term).
๐ Distribution & Appearance
Present in all cells.
1. RER
- Abundant in cells specialized in protein synthesis.
- (Exam Point) โRough = Protein.โ
Light Microscopy (LM):
- Not directly visible.
- If abundant โ cytoplasm appears basophilic (blue) due to RNA in ribosomes binding basic dyes (H&E).
Electron Microscopy (EM):
- Appears as connected tubules/sacs with rough outer surface (ribosomes = dark electron-dense granules).
2. SER
- Abundant in cells with lipid/fat metabolism.
- LM: not visible.
- EM: network of smooth-surfaced tubules.
๐ Functions of ER
1. RER โ Protein Synthesis & Modification
- Step 1: Translation occurs at ribosomes using mRNA from nucleus.
- Step 2: Ribosomes attach to RER; new proteins enter RER tubules.
- Step 3: Proteins undergo initial modification (defects โ hereditary diseases).
- Step 4: Modified protein + RER membrane pinch off โ vesicle.
- Step 5: Vesicle moves to Golgi apparatus for further processing.
(Note: Proteins form structural, enzymatic, and hormonal elements except steroid hormones.)
2. SER โ Lipid & Detoxification Functions
- (Exam Point) Synthesis of lipids, phospholipids, and steroid hormones.
- (Exam Point) Detoxification of toxins & drugs (mainly in liver).
- (Exam Point) Calcium storage in muscle cells for contraction.
๐ II. Mitochondria
๐ Definition
- Known as the Powerhouse of the Cell.
๐ Distribution & Size
- Present in all cells except:
- Red Blood Cells (RBCs)
- Terminal Keratinocytes
- (Exam Point) Size not required for memorization.
๐ Appearance (Light Microscopy)
- Not visible with routine H&E.
- Seen only with special stains (Exam Point):
- Iron Hematoxylin
- Janus Green
- Acid Fuchsin
- Appear as rods or spheres.
๐ Appearance (Electron Microscopy)
- Surrounded by two membranes (double unit membranes).
1. Outer Mitochondrial Membrane (OMM):
- Smooth, permeable.
2. Inner Mitochondrial Membrane (IMM):
- Folded inward โ Cristae (shelf-like structures).
- Selectively permeable.
- Contains Cardiolipin โ responsible for selective permeability.
3. Intermembrane Space:
- Between OMM & IMM.
- Contains Hโบ ions for respiratory chain reactions.
4. Mitochondrial Matrix:
- Fluid inside IMM.
- IMM folds (cristae) โ increase surface area. (Exam Point)
5. F1 Particles (Elementary Particles):
- On IMM surface facing matrix.
- Tennis racket appearance. (Exam Point)
- Contain enzymes for ATP synthesis.
๐ Mitochondrial DNA & Division
- Contains its own DNA โ can divide independently (non-synchronous).
- Mitochondrial DNA:
- Circular shape, in matrix.
- 1% of total cell DNA.
- Nuclear DNA:
- Double helix, in nucleus.
- 99% of total DNA.
๐ Types (EM Classification)
- Orthodox Type: clear cristae & matrix โ resting cells.
- Condensed Type: dense cristae, indistinct matrix โ active cells.
๐ III. Golgi Apparatus (GA)
๐ Definition
- Membranous organelle responsible for secretion. (Exam Point)
๐ Distribution & Location
- Present in all cells.
- Prominent in secretory cells.
๐ Appearance (Light Microscopy)
- Not seen with routine H&E.
- Negative Golgi Image (Exam Point):
- Seen as clear unstained area near nucleus in highly basophilic cells (e.g. plasma cells).
- Special Stains: Silver โ brown filaments (Fittaniya).
๐ Appearance (Electron Microscopy)
- Series of flattened sacs (cisternae/saccules) stacked like plates.
- Two faces:
- Cis / Forming / Convex Face: faces RER & nucleus.
- Trans / Mature / Concave Face: faces cell membrane โ site of secretion.
๐ Functions
- Post-translational modification & packaging of proteins from RER.
- Modification:
- Glycosylation โ glycoproteins.
- Trimming of protein chains.
- Secretion:
- Final vesicles pinch off from Trans face.
- Membrane recycling: forms membranes of RER & cell membrane.
- Lysosome formation: produces lysosomal enzymes.
๐ IV. Lysosomes
๐ Definition
- Digestive system of the cell.
๐ Contents & Origin
- Contain hydrolytic enzymes (digestive enzymes).
- Enzymes synthesized in RER, packaged by Golgi apparatus.
๐ Appearance
- LM: not visible normally.
- EM: membrane-bound vesicles with enzyme content.
๐ Classification (Functional State)
- Primary Lysosome:
- Newly formed, inactive, from Golgi.
- Has not yet fused with target.
- Secondary Lysosome:
- Formed after fusion with a target vesicle.
- Subtypes:
- Phagolysosome: fusion with Phagosome (solid material).
- Multivesicular Body: fusion with Pinocytic vesicle (fluid).
- Autophagic Vacuole: digestion of cellโs own organelles (self-eating).
- Residual Body (Exam Point):
Lipofuscin Pigment (Exam Point): - Indigestible waste left after digestion.
- Normally expelled.
- Accumulates in nerve cells & cardiac muscle cells (non-dividing).
- Represents undigested residual bodies.
๐ Functions
- Digestion & elimination of harmful substances (internal/external).
- Cell metabolism: activates thyroid hormone.
- Post-mortem autolysis:
- After death, lysosomal membranes rupture โ enzymes digest cell โ decomposition.
๐จ Clinical Note
- Lysosomal Storage Diseases: genetic defects in lysosomal enzymes โ substrate accumulation.
- Example: Gaucherโs Disease โ deficiency of Glucocerebrosidase โ buildup of Glucocerebroside in tissues (muscle, brain, joints).
๐ V. Peroxisomes
๐ Definition
- Structurally resemble lysosomes but contain oxidative enzymes.
๐ Contents & Functions
- (Exam Point) Contain oxidative enzymes (vs. lysosomal hydrolytic enzymes).
- Functions:
- Fatty acid oxidation.
- Alcohol detoxification.
- Use oxidative enzymes for metabolism.
๐ Origin
- (Exam Point) Not derived from Golgi apparatus.
๐ Structure (EM)
- Membrane-bound vesicles.
- May appear as coated vesicles (protection from digestion).