Cytoskeleton I Flashcards

1
Q

Alzheimer plaques are surrounded by _____.

A

GFAP-rich reactive astrocytes

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2
Q

The building blocks of MTs are heterodimers of the protein _____ (α and β).

A

tubulin

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3
Q

The three types of _____ are: microfilaments, microtubules, and intermediate filaments.

A

cytoskeletal elements

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3
Q

Abnormal _____ assembly seems to be involved in the neurodegenerative disease, amyotrophic lateral sclerosis (ALS or Lou Gehrig’s Disease).

A

neurofilament

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3
Q

Lamin mutations are linked to various _____.

A

progeria syndroms

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4
Q

____block mitosis and, thus, are important therapeutic tools for cancer treatment.

A

MT toxins

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5
Q

Keratins, a family of about 50 proteins, are dominant components of the _____ and its appendages, providing ____.

A

epidermis; mechanical strength

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5
Q

Abnormal neurofilament assembly seems to be involved in the neurodegenerative disease, _____.

A

amyotrophic lateral sclerosis (ALS or Lou Gehrig’s Disease)

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6
Q

_____ are tubular and are flexible but not very resistant to stretching.

A

Microtubules (MTs)

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6
Q

Mutations in the ______ may interfere with axonal transport and cause Charcot-Marie-Tooth syndrome.

A

neurofilament light chain

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7
Q

The building blocks of ____ are heterodimers of the protein tubulin (α and β).

A

MTs

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8
Q

Vimentins are present in _____.

A

a majority of cell types

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9
Q

Microtubules typically have one end attached to a _____, also known as perinuclear microtubule organizing center (MTOC).

A

centrosome

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9
Q

Several cell-type-specific cytoplasmic IF proteins exist: ____, _____, and _____.

A

keratins, vimentins and vimentin-related proteins, and neurofilament proteins

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10
Q

The _____ provides cell shape, mechanical strength, the structures needed for locomotion, support for the plasma membrane, the scaffold for the spatial organization of organelles, and the means for intracellular transport of organelles and other cargo.

A

cytoskeleton

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11
Q

_____ can lead to epidermolysis bullosa simplex.

A

Keratin mutations

12
Q

Glial fibrillary acidic protein (GFAP) is the IF protein characteristic of astrocytes in the CNS, abundant in connection with ______ in the brain.

A

inflammatory and/or degenerative processes

14
Q

______ are rope-like, fibrous structures of about 10nm diameter prominent in cells exposed to mechanical stress.

A

Intermediate filaments (IFs)

14
Q

Intermediate filaments (IFs) are rope-like, fibrous structures of about 10nm diameter prominent in cells _____.

A

exposed to mechanical stress

14
Q

The main function of ___ is to provide intracellular mechanical support.

A

IFs

15
Q

______ are surrounded by GFAP-rich reactive astrocytes.

A

Alzheimer plaques

17
Q

The main function of IFs is to provide ______.

A

intracellular mechanical support.

18
Q

MT toxins block mitosis and, thus, are important _____.

A

therapeutic tools for cancer treatment

20
Q

The three types of cytoskeletal elements are: ____, _____, and _____.

A

microfilaments, microtubules, intermediate filaments

22
Q

Microtubules (MTs) are _____ and are flexible but not very resistant to _____.

A

tubular; stretching

23
Q

____ mutations are linked to various progeria syndroms.

A

Lamin

25
Q

Several cell-type-specific _____ exist: keratins, vimentins and vimentin-related proteins, and neurofilament proteins.

A

cytoplasmic IF proteins

27
Q

______ typically have one end attached to a centrosome, also known as perinuclear microtubule organizing center (MTOC).

A

Microtubules

28
Q

______ is the IF protein characteristic of astrocytes in the CNS, abundant in connection with inflammatory and/or degenerative processes in the brain.

A

Glial fibrillary acidic protein (GFAP)

30
Q

IFs fall into two categories: ______ and ______.

A

cytoplasmic; nuclear lamins

31
Q

Mutations in the neurofilament light chain may interfere with axonal transport and cause _____.

A

Charcot-Marie-Tooth syndrome

32
Q

____ , a family of about 50 proteins, are dominant components of the epidermis and its appendages, providing mechanical strength.

A

Keratins

33
Q

______ appears to control axonal diameter.

A

Neurofilament abundance

34
Q

Keratin mutations can lead to ______.

A

epidermolysis bullosa simplex

35
Q

____ fall into two categories: cytoplasmic and nuclear lamins.

A

IFs