Tissues 1- epithelial cells Flashcards

1
Q

Where does the variety of cells in the body come from

A

This variety arises as a result of differentiation of precursor cells- they all come from a single zygote

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2
Q

Simply, what is meant by the epithelium

A

Multicellular sheets where the cells are joined together side by side

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3
Q

Describe the contents of the eukaryotic nucleus

A

The contents of the nucleus, the nucleoplasm (Np) and the nucleolus (Nc), are enclosed by a double lipid bilayer, the nuclear envelope (Ne). The unravelled chromosomes (chromatin) are suspended in the nucleoplasm.

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4
Q

What is the nucleolus associated with

A

The invagination of the nuclear envelope

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5
Q

What does the nucleolus consist of

A

The nucleolus is an aggregate of the clusters of rRNA genes that are present at the ends of different pairs of chromosomes (5 pairs in humans: ~300 copies of the rRNA genes). The nucleolus also contains the synthesised rRNA and proteins being assembled to make the ribosome subunits.

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6
Q

Why are there so many copies of the rRNA genes required

A

it is structural, mRNA can make many different proteins, alternate splicing and modifications, rRNA cannot

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7
Q

What do ribosomes consist of

A

Ribosomes are composed of two distinct subunits, each of which contains ribosomal RNA (rRNA) and protein.

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8
Q

Why are the values of S for each subunit not arithmetically additive

A

when the 60S large and 40S small subunits are assembled to make a ribosome, the ribosome is 80S (not 100S). This is because the density and shape of the assembled ribosome contributes to the lower sedimentation coefficient.

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9
Q

Which organelle is continuous with the nuclear envelope

A

The RER

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10
Q

Describe the role of the nuclear lamina in the nuclear envelope

A

The nuclear lamina is a specialised type of cytoskeleton formed on the internal surface of the nuclear envelope. Important in controlling the assembly/disassembly of the nuclear envelope in cell division.

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11
Q

Describe the differences between the RER and the SER

A

SER-Agranular, more tubular sacs, no ribosomes, lipid metabolism
RER-Granular, protein synthesis and transport, ribosomes present

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12
Q

Role of the RER

A

RER is the site of synthesis of membrane proteins and of proteins that are packaged in membrane-bound structures, e.g. secretory vesicles, lysosomes

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13
Q

Role of the SER

A

SER specialises in detoxification and lipid metabolism. The enzymes involved are typically associated with the membranes. SER is also the site of Ca2+-storage in cells (which is important in many cell-signalling contexts).

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14
Q

Describe the arrangement of the Golgi body and how this arrangement allows the Golgi to perform its function

A

The cis face of the Golgi apparatus is aligned to the endoplasmic reticulum, and the trans face is towards the cell periphery.

This arrangement allows the Golgi to receive vesicles from the ER and direct vesicles to the rest of the cell and the cell surface.

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15
Q

What are peroxisomes

A

Peroxisomes are enclosed by a single membrane, and contain enzymes involved in lipid and oxygen metabolism, e.g. oxidases, catalases, peroxidases. Present in most eukaryotic cells.

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16
Q

Describe the appearance of peroxisomes

A

The enzymes present in peroxisomes can be present at such high concentrations that they “crystallise” to form the cores that are observed in transmission EM.

These organelles are important in oxidation reactions. A by-product of many of these actions is peroxide, which is used in peroxidation reactions in many cell types.

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17
Q

Describe the structure of microtubules

A

Polymers of a and b tubulin heterodimers, ~20nm thick.

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18
Q

What is the role of microtubules

A

Involved in cell shape, and act as “tracks” for the movement of organelles and other cytoplasmic components within the cell.
Many accessory proteins involved in these functions.
They are also involved in the formation of the mitotic spindle, hence the microtubular mitotic spindle is the target for many antimitotic cancer drugs.

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19
Q

Where are microtubules found

A

The major component of cilia and flagellae

20
Q

Where do the microtubules radiate from

A

MTs often radiate from a central structure in a cell, the microtubule organising centre (MTOC).

21
Q

Describe the structural arrangement of the microtubules in flagellae

A

9 microtubule doublets and 2 central microtubules make up the core of cilia and flagellae: the 9+2 arrangement.
ATP-dependent motor proteins (blue in the diagram above) distort the cilium or flagellum to produce movement.
Not pairs- hence not fully tubular

22
Q

How does the flagella give bacteria motility

A

Motor proteins bind to microtubules, ATP deforms the microtubules, allowing the motor proteins to walk along it, as the microtubules are fixed in the flagellum, they bend, giving the bacteria motility

23
Q

What are the intermediate filaments

A

A group of polymers of filamentous proteins which form rope-like filaments, with diameter in the range 10-15 nm.

24
Q

Describe the role of the intermediate filaments

A
IFs give mechanical strength to cells. Desmosome cell-cell adhesions are connected by intermediate filaments (cytokeratins in epithelia; desmin in cardiac muscle cells). 
Nuclear lamins (mentioned earlier) are intermediate filaments found forming a network on the internal surface of the nuclear envelope, being involved in stabilising the envelope.
25
Q

Describe the different types of intermediate filaments found in different cell types

A

epithelia have cytokeratins;
mesenchymal cells have vimentin;
neurones have neurofilament protein.
muscle cells have desmin.

26
Q

What are the microfilaments

A

Polymers of the globular protein, actin; associate with adhesion belts in epithelia and endothelia, and with other plasma membrane proteins.
5-9nm diameter

27
Q

Describe the role of the microfilaments

A

Involved in cell shape and cell movement (crawling of cells; cell contractility esp. muscle).
Accessory proteins, e.g. myosin, act with actin to control actin organisation and cell movement.
In addition to being a major component of the contractile apparatus of muscle. Actin microfilaments are involved in the contraction of non-muscle cells.

28
Q

What are the monomers in actin and microfilament

A

Monomer = globular actin, G-actinMicrofilaments = filamentous actin, F-actin

29
Q

Where is the actin normally found

A

Typically present in the cortical (peripheral) regions of a cell.

30
Q

Describe the main cell type groups

A

Connective tissue cells: fibroblasts (many tissues), chondrocytes (cartilage), osteocytes (bone).
Contractile tissues: skeletal muscle, cardiac muscle, smooth muscle.
Haematopoietic cells: blood cells, tissue-resident immune cells, and the cells of the bone marrow from which they are derived.
Neural cells: cells of the nervous system having two main types; neurones (carry electrical signals) and glial cells (support cells).
Epithelial cells: cells forming continuous layers, these layers line surfaces and separate tissue compartments and have a variety of other functions.

31
Q

Describe the different types of tumour that arise from different cell types

A

epithelial cancers are carcinomas

mesenchymal (connective tissue and muscle) cancers are sarcomas

haematopoietic cancers are leukaemias (from bone marrow cells) or lymphomas (from lymphocytes)

neural cell cancers are neuroblastomas (from neurones) or gliomas (from glial cells)

32
Q

What is a tissue

A

a group or groups of cells whose type, organisation and architecture are integral to its function
tissues are made up of cells, extracellular matrix and fluid

33
Q

What is the ECM

A

material deposited by cells which forms the “insoluble” part of the extracellular environment
generally composed of fibrillar (or reticular) proteins (e.g. collagens, elastin) embedded in a hydrated gel (proteoglycans or “ground substance”)
may be poorly organised (e.g. loose connective tissue) or highly organised (e.g. tendon, bone, basal lamina)

34
Q

Describe epithelial organisation

A

epithelial cells make organised, stable cell-cell junctions to form continuous, cohesive layers

epithelial layers line internal and external body surfaces and have a variety of functions, e.g. transport, absorption, secretion, protection

cell-cell junctions key to the formation and maintenance of epithelial layers

35
Q

Describe simply how continuous layers of epithelial cells can form

A

continuous epithelial layers can form because cells make stable cell-cell junctions which give the epithelia mechanical integrity and act to seal the intercellular pathways of the layer.

in many epithelia these are found at the apical region of cell-cell contact as a junctional complex.

generally in 2 forms: zonulae (belts) or maculae (spots)

36
Q

Describe cell-cell junctions in epithelia

A

typically arranged as an apical junctional complex containing a tight junction nearest the apex, then an adhesion belt, then, scattered throughout the lateral membrane, desmosomes (spot adhering junctions)

other important junctions are gap junctions, which act as regions of direct communication between adjacent cells

37
Q

Describe the formation of tight junctions

A

The tight junction is formed by proteins called claudins and occludins, which are arranged in strands along the lines of the junction to create the seal.zonula occludens (belt 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

38
Q

What are the roles of the tight junction

A

act to seal paracellular pathways (i.e. between cells)- without junctions to prevent leakage, the pumping activities of absorptive cells such as those around the gut would be futile, and the composition of fluids on both sides of the epithelium would be the same

The tight junctions also play a key part in maintaining the epithelial polarity of the epithelial cells

The tight junctions around the apical region prevents the diffusion of proteins within the plasma membrane and so keeps the apical domain biochemically different from the basolateral domain.

The tight junctions are also sites for the assembly of proteins which separate the apical and basolateral domains.

39
Q

Describe the adhesion belt

A

zonula adherens (belt junction, adherens junction (AJ))
usually formed just basal to the apical tight junction
transmembrane adhesion molecule is a cadherin (family of Ca2+-dependent cell adhesion molecules)
Cadherin of one cell binds directly to an identical cadherin molecule in its neighbour,
cadherins associate with the microfilament (actin) cytoskeleton- via several linker proteins
this junction controls the assembly of the other junctions (“master junction”)

40
Q

What is the role of the adhesion belt

A

Bundles of actin filaments are connected from cell to cell across the epithelium, this network can contract, giving the epithelial sheet to develop tension and change its shape. By shrinking the epithelial sheet along one axis, the sheet can roll into a tube. Alternatively, by shrinking the apical surface locally along all axes at once, the sheet can invaginate into a cup and eventually create a vesicle by pinching off from the rest of the epithelium.- important in the development of the embryo

41
Q

Describe the desmosomes

A

macula adherens (spot desmosome)
found at multiple spots between adjacent cell membranes
transmembrane cell adhesion molecule is a cadherin-like molecule
linked to the intermediate filament cytoskeleton- keratin filaments
provides good mechanical continuity between cells

42
Q

Describe the gap junction

A
macula communicans (spot junction)
made up of clusters of pores formed from 6 identical subunits in the membrane - these pores are continuous with pores in adjacent cell membrane
allows passage of ions and small molecules between cells
pH, Ca2+ conc, voltage, and some signalling molecules can affect passage, i.e. can open and close pores thereby controlling intercellular communication
also known as the electrical synapse; important in the passage of electrical signals in some tissues
43
Q

Describe how gap junctions appear

A

As a region where the membranes of two cells lie close together and are parallel, with a very narrow gap between them.

44
Q

What does the gap consist of

A

It is spanned by the protruding ends of identical, trans-membrane complexes called connexons, which are aligned end to end to form water-filled channels across the two plasma membranes. These channels allow the passage of inorganic ions and small water-soluble substances below a molecular mass of 1000, to move directly between the cytosol of the two cells, creating an electrical and metabolic coupling between the cells.

45
Q

Describe the importance of the gap junction in cardiac cells

A

Allows the electrical waves of excitation to spread synchronously throughout the heart, triggering a coordinated contraction

46
Q

Describe the role of the gap junction in synapses

A

synapses mainly in neural tissue (i.e. not epithelial)
button-like junctions formed between neurones or between neurones and target cells (e.g. muscle)
information passed one-way via a chemical signalling system
a variety of chemical signals and receptors are utilised at synapses
Gap junctions can be open or closed in response to extracellular or intracellular signals.