Lecture 3 Flashcards

1
Q

How is E-cadherin linked to the cytoskeleton?

A

Linked indirectly to cytoskeleton through adaptor proteins

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2
Q

What is beta-catenin

A

an adaptor protein

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3
Q

If there is an increase in N-cadherin what will happen to the cell?

A

Go through EMT

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4
Q

describe the interactions of hemidesmosomes and desmosomes?

A

Desmosomes: Cell-cell interactions through cytoplasmic plaque
Hemidesmosomes: Cell-matrix interactions, binds to alpha-beta integrin which links to adaptor protein linking hemidesmosomes to the intermediate filaments

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5
Q

whats a tight junction?

A

Prevents free exchange of solutes: gate function
maintain polarity separates apical and basolateral end: fence function

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6
Q

what are the 4 classes of tissues

A

Muscle, Epithelial, Connective, Neural

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7
Q

what are the functions of epithelial tissue?

A

Protection from physical and chemical injury
Protection against microbial invasion
Contains receptors which respond to stimuli
Permeability barrier: filters, secretes & reabsorbs materials
Secretes serous fluids to lubricate structures.

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8
Q

What are the classifications of epithelial

A

According to thickness/ layers: simple (one layer), stratified (more than one layer)
According to shape: Squamous (wider than tall), Cuboidal (as tall as wide), columnar (taller than wide)

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9
Q

What are the differences between benign and malignant tumours

A

Benign: Primary location, distinct borders, grow slow
Malignant: grow uncontrollably, irregular shape and border, spread, metastasis can occur anywhere in body
Requires urgent treatment

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10
Q

What is neoplasm?

A

new growth that can be benign or malignant

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11
Q

types of neoplasia

A

Atrophy, hypertrophy, hyperplasia (increased numbers), metaplasia (conversion o f one type to another), dysplasia

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12
Q

what are the termination differences between epithelial and mesenchymal (connective) benign and malignant forms?

A

Epithelial:
- benign: ends in oma
- Malignant: ends in carcinoma
Mesenchymal:
- Benign: ends in oma
- Malignant: ends in sarcoma

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13
Q

are carcinomas or sarcomas more common?

A

Carcinomas

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14
Q

what are the 3 types of proteins that constitute tight junctions? What happens when you remove each one?

A

Occludin: no phenotype change
Claudins: lethal
JAM: increased intestinal epithelial proliferation

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15
Q

What is the function of Claudins?

A

20-27 kDa, Signaling pathways by C-terminal interaction with signaling molecules

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16
Q

The function of GAP junctions? Structure?

A

cylinders of six dumbbell-shaped connexin molecules (26-60 kDa)
12 connexin molecules
Allows passage of ions and molecules smaller than 1200 Da
Transmission of ionic signals in heart-muscle contraction
Transmission of ionic signals
secondary messenger

17
Q

What are the 2 classes of epithelial cells? 7 subclasses?

A

simple: squamous, cuboidal, columnar
Stratified: squamous, cuboidal, pseudostratified columnar, transitional

18
Q

2 types of connective tissue? (2 extras)

A

bone, blood,
extra: cartilage, fibrous

19
Q

what’s the functions of epithelial tissue

A

protection from physical/chemical injury, protection against microbes, response to stimuli, permeability barrier, lubricate structures

20
Q

whats adenocarcinoma?

A

dunno

21
Q

describe sarcomas from connective tissues, hematopoeitic tissues, and central and peripheral nervous systems?

A

connective: arise from non-epithelial cells, connective tissues, mesoderm origin, 1% of tumours
Hematopoeitic: blood-forming, arise from non-epithelial, embryonic mesoderm origin, erythrocytes, plasma cells, white blood cells, B and T lymphocytes, 7% of mortality of cancer
Nervous: Neuroectodermal tumors, 1.3% of all diagnoses, 1.% of cancer deaths