1 Epithelial Cells Flashcards

1
Q

Q: What is the structure of the nucleus? Pores?

A

A: The nuclear envelope is a double membrane -> The nuclear envelope is continuous with the ER

Nuclear pores are complexes, they are not just holes in the membrane

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Q: What are the 2 types of ER? Role?

A

A: rER - exists as flattened sheets which is studded on its outer surface with ribosomes-> membrane protein synthesis/ those that need to be exocytosed

sER - more tubular and lacks ribosomes. It has a major function in lipid metabolism + detoxification // also site of Ca 2+ storage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Q: What is the nucleolus made of? Function? Contains?

A

A: nucleolus = aggregate of the clusters of rRNA genes

Nucleolus - site of production of subunits of ribosome

also contains the synthesised rRNA + proteins being assembled to make ribosome units

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Q: Why are there many copies of rRNA genes required?

A

A: need many to reach demands of cells (since each one can only produce one rRNA at a time)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Q: What are ribosomes made of? Where do they reside? (2) Difference?

A

A: made of 2 distinct subunits each contains ribosomal RNA and a protein

can be free in cytoplasm- make cytoplasmic proteins

or attached to rER/outer membrane of nucleus- make membrane proteins and proteins to be packaged in membranous organelles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Q: What is the role of ribosomes?

A

A: organelles that read messenger RNA mRNA to synthesise polypeptide chains

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Q: What is a nuclear pore? Role?

A

A: protein complex- large pores contain elaborate arrangements of associated proteins

control import and export of macromolecules into and out of the nucleus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Q: What is the relationship between the nuclear envelope and the ER?

A

A: physical continuity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Q: What is the nuclear lamina? Importance? Targeted when and why?

A

A: specialised type of cytoskeleton (intermediate filaments) formed on the internal surface of the nuclear envelope

important in controlling the assembly/dissembly of the nuclear envelope in cell division

during cell division - when targeted-> modified and allowed breakdown of nuclear membrane (fragments reassemble after cell division)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Q: Describe the Golgi apparatus structure. Function? Direction?

A

A: Stacked, membrane bound, flattened sacs involved in modifying, sorting, and packaging macromolecules for secretion or for delivery to other organelles

cis side is alligned to ER and trans to cell periphery -> allows GA to receive vesicles from ER and direct them to rest of cell and cell surface

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Q: Describe mitochondrion role. Number in a cell indicative of? Structure?

A

A: Energy metabolism - production of ATP - the number of mitochondria you see in a cell is indicative of the cell’s metabolic activity

cristae
mito matrix
intermembrane space

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Q: What are peroxisomes? Importance?

A

A: enclosed in single membrane

contain enzymes involved in lipid and oxygen metabolism e.g. catalases, peroxidases

in oxidation reactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Q: What is phagocytosis?

A

A: cell eating - internalisation of particles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Q: What is pinocytosis?

A

A: cell drinking - extracellular fluid is internalised - major function: receptor mediated endocytosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

*Q: What is the cytoskeleton? Why described as dynamic?

A

A: A system of 3 types of filaments formed by the polymerisation of protein monomers

microfilaments
intermediate filaments
microtubules

Dynamic =The cytoskeleton is NOT FIXED. The various elements of the cytoskeleton are subject to rapid remodelling by a variety of biochemical and bio-mechanical signals

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

*Q: Describe microfilaments. Monomer? Structure? Role? Which accessory proteins associate with it? Usually bundled where?

A

A: Monomer = Globular Actin (G-actin)

Polymers of actin associate with adhesion belts in epithelia and endothelia and with other plasma membrane proteins -> helical structure

Involved in cell shape and cell movement (crawling and contractility)

Accessory proteins which associate with actin =myosin

Usually bundled near the periphery of the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

*Q: Describe intermediate filaments. Monomer? Diameter? Role?

A

A: A group of polymers of filamentous proteins which form rope-like filaments

Diameter - 10-15nm

give mechanical strength to the cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

*Q: Describe microtubules. Monomer? Diameter? Role? Radiate out from?

A

A: Polymers of a and b tubulin

~20nm in diameter

Involved in cell shape and act as tracks for the movement of organelles and cytoplasmic components within the cell.
Motor proteins are necessary for this movement.

Typically, microtubules tend to radiate out from a particular point within a cell.
That point is called the Microtubule Organising Centre (MTOC).

19
Q

*Q: Which cytoskeleton component is part of spindle fibres in mitosis?

A

A: Microtubules

20
Q

*Q: Which cytoskeleton component is the major structural component of cilia and flagellae?

A

A: Microtubules

9 and 2 formation in both

21
Q

*Q: What are the main cell types? (5)

A

A: Epithelial Cells - cells forming continuous layers - the layers line surfaces and separate tissue compartments.

Mesenchymal Cells - connective tissue - e.g. fibroblasts, chondrocytes, osteocytes, muscle cells

Haematopoietic Cells - blood cells and cells of the bone marrow from which they are derived

Neural Cells - nervous system - 2 main types: neurones (carry electrical signals) and glial cells (support cells)

contractile tissues- skeletal muscle, cardiac muscle, smooth muscle

22
Q

*Q: Give examples of how tumours retain characteristics of the cell type from which they originated? (4)

A

A: Epithelial Cancers = Carcinoma

Mesenchymal Cancers = Sarcomas

Haematopoietic Cancers = Leukaemias (bone marrow cells) + Lymphomas (lymphocytes)

Neural Cancers = Neuroblastomas (neurones) + Gliomas (glial cells)

23
Q

*Q: Describe ‘tissue’. Made of?

A

A: a group of cells whose type, organisation and architecture are integral to its function

Tissue = Cells + Extracellular Matrix + Fluid

24
Q

*Q: What is the extracellular matrix? Definition. Generally composed of? What is the organisation?

A

A: Definition - the insoluble material that you will find extracellularly

generally composed of fibrillar (or reticular) proteins (e.g collagen, elastin) embedded in a hydrated gel (proteoglycans or ‘ground substance’).

may be poorly organised (eg loose connective tissue) or highly organised (tendons and bone and basal lamina)

25
Q

*Q: What is the organisation of epithelium? Line? What’s their function? What’s key to maintenance and formation?

A

A: Epithelial cells form layers - because they form stable cell-cell junctions - allows them to form cohesive layers

Line body surfaces externally and internally

Involved in transport, absorption, secretion and protection

cell-cell junctions

26
Q

*Q: What do cell-cell junctions allow to form? Found?

A

A: Continuous epithelial layers can form because cells make stable cell-cell junctions

in many epithelia, the cell-cell junctions are found in the apical region of cell-cell contact as a junctional complex

27
Q

*Q: What are the 2 forms of cell-cell junctions in epithelia?

A

A: Zonulae (belts) and Maculae (spots)

28
Q

*Q: Describe the junctional complex arrangement in epithelial tissue. Another important junction?

A

A: typically arranged:

tight junction nearest the apex
adhesion belt
desmosomes= scattered throughout the lateral membrane (spot adhering junctions)

gap junctions- act as regions of direct communication between adjacent cells

29
Q

*Q: Describe tight junctions. Another name?

A

A: Zonula Occludens (occluding junction)

points on adjacent membranes form close contacts at apical lateral membranes

form a network of contacts, the more elaborate the network, the tighter the seal

act to seal paracellular pathways (ie between cells)

segregates apical and basolateral membrane polarity

30
Q

*Q: Describe the adhesion belt. Another name? Formed where? What helps them form? What’s closely associated with it?

A

A: Zonula Adherens

Formed just basal to the apical tight junction.

transmembrane adhesion molecule = Cadherins - bind to similar molecules on the adjacent cell and cluster (with the help of actin) to form these junctions

The actin cytoskeleton is closely associated with these junctions.

controls the formation of other junctions (once it forms itself) hence it is the Master Junction

31
Q

*Q: Describe demosomes. Another name? Found where? What helps adhesion? Linked to? Provides?

A

A: desmosomes = Macula Adherens - SPOT junction

They are dotted around the lateral membrane between cells

They have cadherin-like-molecules which are involved in transmembrane cell adhesion

Desmosomal Cadherins link to the intermediate filament cytoskeleton

provides good mechanical continuity between cells

32
Q

*Q: Describe gap junctions. Another name? Made of? Allow passage of? What can control? Also known as? esp important in which cells?

A

A: macula communicans (spot junction)

Made up of clusters of pores which are formed of
6 identical subunits in the membrane

pores are continuous with pores on adjacent membranes

Allow the passage of ions and small molecules between cells- direct cell communication

pH, Ca 2+ conc, voltagea and some signally molecules can affect passage ie open and close pores thereby controlling intercellular communication

also known as the electrical synapse- important in the passage of electrical signals in some tissues (can conduct signal between cells esp important in cardiac cells)

33
Q

*Q: Describe (chemical) synapses. Found mainly in? Formed where? Information passed?

A

A: Found in neural tissue - not epithelial

button like junctions formed between neurones or their targets eg muscle

Pass information in one direction (chemical signalling system)

34
Q

Q: What is heterochromatin?

A

A: regions of condensed DNA (less active)

35
Q

Q: What are cisternae?

A

A: flattened sacs of membrane of the endoplasmic reticulum (and GA)

36
Q

Q: Cells with lots of sER?

A

A: high steroid production usually

37
Q

*Q: What is the arrangement of microtubules?

A

A: 9 mt doublets and 2 central mt make up core of cilia and flagellae: 9+2 arrangement

38
Q

*Q: What are cell-cell junctions capable of? Controlled by?

A

A: changing their assembly and organisation (laible)

dynamic assembly and disassembly = controlled by variety of factors in health and disease

39
Q

Q: Approximately how many cell types are there in the human body?

A

A: 200

40
Q

*Q: Demonstrate the following on a suitable transmission
electron micrograph: nucleus; nucleolus; nuclear
envelope; mitochondrion; rough endoplasmic reticulum;
smooth endoplasmic reticulum; ribosomes; Golgi
apparatus; secretory granule; plasma membrane;
cytoskeletal components.

A

A: REFER

41
Q

*Q: What is a brush border?

A

A: microvilli-covered surface of simple cuboidal epithelium and simple columnar epithelium cells

42
Q

*Q: What is cilia? role? (2)

A

A: short microscopic hair-like vibrating structure found in large numbers on the surface of certain cells, either causing currents in the surrounding fluid, or, in some protozoans and other small organisms, providing propulsion

43
Q

*Q: features of epithelial cells: apical surface; basolateral surface; brush border; microvilli; cilia; cell junction; basal lamina (basement membrane). Demonstrate them on suitable transmission electron micrographs.

A

A: REFER