Chapter 20 Flashcards

1
Q

describe epithelial tissue (3)

A

also called epithelium =multicellular sheets in which epithelial cells are joined
-cells have different shapes and can be single layer or multi-layered
-epithelia covers external surfaces of body and line cavities/organs

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2
Q

describe epithelium cell polarity

A

-epithelial cells are polarized : apical and basal(basolateral) sides

apical = upper & free /could have cilia etc
baso= lower and attached to basal lamina

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3
Q

epithelial sheets rest on a ___ ____ which consists of ……

A

epithelial sheets rest on a basal lamina which consists of collagen and laminin atop connective tissue

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4
Q

what are the 3 types of intercellular junctions

A

anchoring junctions: (strongest/ distribute stress)
-desmosomes
-adherens
-hemidesmosomes

tight junctions: (waterproofing)

gap junctions: (movement of solutes)

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5
Q

what do intercellular junctions do

A

hold cells together

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6
Q

what are cadherins

A

link two separate cells together and are tethered via linker proteins that attach to actin filaments inside the cell
-form a belt-like structure around epithelial cells

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7
Q

what are desmosomes

A

-bind epithelial cells in sheets / allow keratin of adjoining cells to be connected
-great tensile strength

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8
Q

what are hemidesmosomes

A

-bind epithelial cells to basal lamina via integrins

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9
Q

what are integrins

A

adhere the cells to basal lamina / joined to the keratin filaments via linker proteins

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10
Q

describe the orders of each anchoring junction

A

desmosomes
= keratin - linker (cytoplasmic plaque) - cadherins

hemidesmosomes
= keratin - linker (cytoplasmic plaque) - integrins

adherens
= actin - linker - cadherins

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11
Q

describe tight junctions

A

=waterproofing / provide a tight seal

-help polarize cells
-bound by occludin/claudin protein complexes

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12
Q

how can movement of proteins be restricted in the cell

A

cell junctions particularly tight junctions

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13
Q

describe gap junctions

A

-function in communication between neighboring cells
-allow for inorganic ions and small water soluble molecules to pass from one cell to another
~they pass between pores formed by connexon complexes
-open/close in response to extracellular signals

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14
Q

describe cancer

A

develops do to an accumulation of mutations that blow past checkpoints

~cancer cells are genetically unstable
-one cell requires an mutation that gives it an advantage over its neighbors / the daughter cells of the best adapted cells then continue to divide becoming the dominant clone in the developing tumor
*Ras

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15
Q

what are the two types of cancer mutations

A

-oncogenes
-tumor suppressor genes

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16
Q

what is metastases

A

-secondary tumors

17
Q

tumors that metastasize are called ___ ____

A

malignant tumors

18
Q

describe oncogenes

A

when there is a mutation in a proto-oncogene its called an oncogene
=gain of functions (dominant)

-mutation in one allele is sufficient
-increases risk of cancer as gas pedal is permanently on

19
Q

describe tumor suppressor genes and give examples

A

turn into inactive tumor suppressor genes when mutated
=loss of function (recessive)

-both alleles mutated (turned off)
-brakes don’t work
-increases levels of cyclin-Cdks when dont want them

ex. Rb, p53, APC

20
Q

describe case study progeria

A

-mutation into S phase that doesn’t get repaired on chr. 1 / large amounts of progerin
-effects lamins
-C–>T but gets missed
-loss of 150bp / 50 AAs from cyptic 5’ splice site

21
Q

what’s a cryptic splice site

A

adds an extra splice site

22
Q

what does progeria affect

A

affects breakdown and reformation of nuclear envelope