Intro to microscopic anatomy Flashcards

(56 cards)

1
Q

What are the two colors commonly associated with Haematoxylin & Eosin (H&E) staining?

A

Pink and purple.

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2
Q

What does Haematoxylin stain in tissue samples?

A

Haematoxylin stains acidic (or basophilic) structures such as DNA (nucleus, nucleolus), RNA, and carbohydrates (cartilage molecules).

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3
Q

What does Eosin stain in tissue samples?

A

Eosin is an acidic dye that stains basic (or acidophilic) structures, such as cytoplasmic proteins and extracellular fibers.

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4
Q

What is the cell shape of squamous epithelium?

A

Flat

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5
Q

Where can squamous epithelium be found in the body?

A

Heart, lungs, blood vessels (endothelium), and membranes (mesothelium).

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6
Q

What are the functions of squamous epithelium?

A

Diffusion, filtration, and secretion.

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7
Q

What is the cell shape of cuboidal epithelium?

A

Cube-like.

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8
Q

Where can cuboidal epithelium be found in the body?

A

Glands and kidney tubules.

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9
Q

What are the functions of cuboidal epithelium?

A

Secretion and absorption.

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10
Q

What is the cell shape of columnar epithelium?

A

Rectangular.

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11
Q

Where can columnar epithelium be found in the body?

A

Gastrointestinal tract and uterine tubes.

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12
Q

What are the functions of columnar epithelium?

A

Absorption and secretion.

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13
Q

What is the cell layer of simple epithelium?

A

Single layer.

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14
Q

Where can simple squamous epithelium be found in the body?

A

Heart, lungs, blood vessels, and membranes.

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15
Q

What is the cell layer organization of stratified epithelium?

A

More than one layer.

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16
Q

What are the subtypes of stratified epithelium?

A

Squamous, Keratinized (K), and Non-keratinized (NK).

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17
Q

Where can keratinized stratified squamous epithelium be found in the body?

A

Skin.

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18
Q

Where can non-keratinized stratified squamous epithelium be found in the body?

A

Mouth.

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19
Q

What is the main function of stratified epithelium?

A

Protects against injury.

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20
Q

What is the cell layer organization of transitional epithelium?

A

Variable number of cell layers.

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21
Q

Where can transitional epithelium be found in the body?

A

Urinary system - Bladder and Urethra.

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22
Q

What is the main function of transitional epithelium?

A

Allows stretching of the lining.

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23
Q

What is the characteristic of epithelial tissue regarding cell turnover and tissue renewal?

A

Epithelial tissue is characterized by high cell turnover and tissue renewal.

24
Q

What are examples of epithelial tissues that undergo self-renewal?

A

Epidermis (skin), small intestine.

25
What is the dependence of epithelial tissue self-renewal on?
Epithelial tissue self-renewal depends on the activity of tissue-specific stem or progenitor cells.
26
Can you provide examples of tissue-specific stem or progenitor cells involved in epithelial tissue self-renewal?
Intestinal Stem Cells (characterized by the protein Lgr5), Hair follicle cells, Lung epithelium.
27
What risks are associated with the ability of epithelial tissue to renew?
The emergence of benign tumors (adenomas) and malignant transformation leading to cancers such as carcinomas or adenocarcinomas.
28
What can happen if the epithelium is damaged faster than its renewal capability?
It can result in impaired organ function, such as celiac disease due to an autoimmune response.
29
What is the function of adipose tissue (fat tissue)?
Adipose tissue provides protection for internal organs, insulation, and acts as an energy store.
30
What are the components of blood?
Blood consists of white blood cells (defense), red blood cells (oxygen transport), proteins, fibers (fibrin - for haemostasis), and blood plasma (non-cellular component).
31
What is the function of blood plasma?
Blood plasma is essential for the transport of nutrients and molecules to different tissues and cells in the body.
32
How are glands "constructed"?
Glands are constructed from epithelial cells, including specially adapted secretory epithelial cells.
33
What are the two main types of glands?
The two main types of glands are exocrine glands and endocrine glands.
34
What is the difference between exocrine and endocrine glands?
Exocrine glands have ducts through which they release their secretions onto the surface of the epithelium, while endocrine glands are ductless and release their secretions directly into the bloodstream.
35
Give an example of a unicellular gland.
Goblet cells in the intestinal and respiratory epithelium are examples of unicellular glands.
36
Give examples of multicellular glands.
Examples of multicellular glands include salivary glands, sebaceous glands, and sweat glands.
37
How do unicellular glands and multicellular glands differ in their secretory mechanism?
Unicellular glands, such as goblet cells, secrete directly onto the surface of the epithelium, while multicellular glands secrete through a duct that opens onto the surface of the epithelium.
38
What are the main components involved in gland structure?
Glands consist of secretory epithelial cells (both unicellular and multicellular) and may have a duct system for transporting secretions.
39
What is autophagy?
Autophagy is the process of self-eating, involving the digestion of cytosol, molecules (such as proteins), and worn-out organelles within cells.
40
How is autophagy completed?
Autophagy is completed through the action of lysosomes, which contain digestive enzymes called acid hydrolases.
41
What are the two types of autophagy?
Autophagy can be non-selective, employed during times of starvation, or selective, employed to remove specific cell components during periods of growth, differentiation, or removal of surplus or worn-out organelles.
42
What is the role of autophagy in innate immunity?
Autophagy plays a role in innate immunity as a response to infection.
43
What is the function of lysosomes?
Lysosomes contain digestive enzymes that can break down biomolecules such as proteins, nucleic acids, lipids, and sugars. They create a low pH environment for enzymatic activity.
44
What are melanosomes?
Melanosomes are a special category of lysosomes found in melanocytes. They hold melanin pigments and contribute to skin pigmentation by secreting melanin through exocytosis.
45
How does autophagosome formation occur?
A portion of the cytoplasm is surrounded by a double membrane, creating an autophagosome. This autophagosome then fuses with a lysosome, leading to the degradation of biomolecules or organelles.
46
What is the role of cell metabolism signaling pathways in autophagosome formation?
Cell metabolism signaling pathways play a role in the regulation and control of autophagosome formation.
47
How are damaged mitochondria removed from cells?
Damaged mitochondria are removed through a process called mitophagy, which involves selective autophagy of mitochondria.
48
What happens when biomolecules or entities enter a cell by endocytosis?
Endosomes fuse with lysosomes, creating endolysosomes for the degradation of the internalized biomolecules or entities.
49
What can happen if the autophagy process is impaired?
Impairment of the autophagy process can lead to the accumulation of molecules in lysosomes, such as the accumulation of tau proteins in neurodegenerative disorders.
50
How is impaired mitophagy linked to a form of early onset Parkinson's disease?
Impaired mitophagy, which is the degradation of mitochondria through autophagy, is linked to a form of early onset Parkinson's disease.
51
What are lysosomal storage diseases?
Lysosomal storage diseases are genetic disorders that result in the accumulation of undigested biomolecules within lysosomes.
52
How does aging affect autophagy?
During aging, autophagy gradually declines, which may contribute to the accumulation of cellular waste products and dysfunctional organelles.
53
What is the role of autophagy in neurodegenerative disorders?
Autophagy plays a role in the removal of abnormal protein aggregates, such as tau proteins, and impairment of autophagy can contribute to the accumulation of these proteins in neurodegenerative disorders.
54
How does impaired mitophagy contribute to Parkinson's disease?
Impaired mitophagy can lead to the accumulation of dysfunctional mitochondria, which is implicated in the pathogenesis of Parkinson's disease.
55
What is the main cause of lysosomal storage diseases?
Lysosomal storage diseases have a genetic cause, typically resulting from mutations in genes that encode lysosomal enzymes or proteins involved in lysosomal function.
56
What are the consequences of lysosomal storage diseases?
Lysosomal storage diseases result in the accumulation of undigested biomolecules within lysosomes, leading to cellular dysfunction and tissue damage.