CHAPTER 1 Pt. 2 Histology and Its Methods of Study Flashcards

1
Q

Cell surface glycoproteins and mucin are
PAS-positive because of their high content of ___________
and _________

A

oligosaccharides; polysaccharides

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2
Q

LESS common method of staining

A

Metal Impregnation

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3
Q

Metal Impregnation uses ______ or ______ to have visual certain ECM fibers and specific cellular components in nervous tissue such as dendrites or dendritic spines

A

silver; gold

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4
Q

Metal Impregnation for Cerebral Cortex exposes what component?

A

cytoplasmic process

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5
Q

We avoid these dyes for metabolic diseases diagnosis that intracellular accumulations of cholesterol, phospholipids, or glycolipids

A

Lipin Soluble Dyes such as Sudab black

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6
Q

it is a modification of PAS procedure; stains DNA of cell nuclei

A

Feulgen Reaction

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7
Q

Slide preparation, from tissue fixation to observation
with a ______________, may take from 12 hours to 2½ days,
depending on the size of the tissue, the embedding medium,
and the method of staining.

A

light microscope

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8
Q

The final step before microscopic
observation is mounting a __________________________ on the
slide with clear adhesive.

A

protective glass coverslip

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9
Q

The optical
components of a bright-field microscope

A

condenser
objective
eyepiece

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10
Q

focusing light on the object
to be studied

A

condenser

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11
Q

lens enlarging and projecting the
image of the object toward the observe

A

objective

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12
Q

further magnifying this image and projecting
it onto the viewer’s retina or a charge-coupled device

A

eyepiece/ocular lens

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13
Q

The total magnification is obtained by multiplying the_______________ and ____________

A

magnifying power of the objective and ocular lenses.

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14
Q

The critical factor in obtaining a crisp, detailed image
with a light microscope is its

A

resolving power

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15
Q

defined as the
smallest distance between two structures at which they can be
seen as separate objects.

A

resolving power

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16
Q

The maximal resolving power of the
light microscope is approximately

A

0.2 μm

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17
Q

maximal resolving power can permit
clear images magnified __________ times

A

1000-1500

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18
Q

Objects smaller or
thinner than 0.2 μm cannot be distinguished with this instrument.

A

light microscope

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19
Q

typically used for study of bright-field microscopic preparations, involves the conversion of a stained tissue preparation to high-resolution digital images
and permits study of tissues using a computer or other digital device, without an actual stained slide or a microscope.

A

Virtual microscopy

20
Q

When certain cellular substances are irradiated by light of a
proper wavelength, they emit light with a longer wavelength—
a phenomenon called

A

fluorescence

21
Q

tissue sections are usually irradiated with ultraviolet (UV) light and the emission is in the visible portion of
the spectrum.

A

fluorescence
microscopy

22
Q

Acridine orange binds nucleic acids and causes DNA in cell
nuclei to emit _________ light and the RNA-rich cytoplasm to
appear ______ in these cells of a kidney tubule.

A

yellow; orange

23
Q

DAPI

A

(4′,6-diamino-2-phenylindole)

24
Q

Cultured cells stained with DAPI (4′,6-diamino-2-phenylindole)
that binds DNA and with fluorescein phalloidin that binds actin
filaments show nuclei with ____ fluorescence and actin filaments
stained _____.

A

blue; green

25
Q

Living neural crest cells growing in culture
________: Without fixation and staining, only
the 2 pigment cells can be seen.

A

Bright-field microscopy

26
Q

Cell boundaries, nuclei, and
cytoplasmic structures with different refractive indices affect
in-phase light differently and produce an image of these features
in all the cells

A

Phase-contrast microscopy

27
Q

Cellular details
are highlighted in a different manner using Nomarski optics.
Phase-contrast microscopy, with or without differential interference, is widely used to observe live cells grown in tissue culture

A

Differential interference contrast microscopy

28
Q

in a bright field microscope, excess light reduces contrast within the image and compromises the resolving power of the objective lens, what specific type of microscopy avoids these problems?

A

Confocal microscopy

29
Q

Confocal microscopy achieves high resolution and sharp focus by using
(1) a small point of _____________, often from a laser and
(2) a plate with a
_________ aperture in front of the image detector.

A

high-intensity light; pinhole

30
Q

allows the recognition of stained or
unstained structures made of highly organized subunits

A

Polarizing microscopy

31
Q

The ability to rotate the direction
of vibration of polarized light is called

A

birefringence

32
Q

DIFFERENT MICROSCOPIES UNDER LIGHT MICROSCOPY?

A

Bright-field
Fluorescence
Phase-Contrast
Confocal
Polarizing

33
Q

this type of microscopy has longer wavelength, less distinction

A

Light Microscopy

34
Q

it has black background; white/clear vision of the tissue components; used to detect ________

A

Dark-field Microscopy; syphilis

35
Q

scan tissues at different level; reconstruct 3d image

A

confocal

36
Q

like an x-ray; 2d

A

transmission electron microscopy

37
Q

x-ray but 3d

A

scanning electron microscopy

38
Q

In polarizing Microscopy, there is an intense color of yellow, or orange birefringence. What component of the sample are these colors?

A

collagen fibers for unsectioned mesentery

39
Q

The wavelength in an electron beam is much shorter than that
of light, allowing a 1000-fold increase in resolution.

A

ELECTRON MICROSCOPY

40
Q

an imaging system that permits resolution around 3 nm

A

Transmission Electron Microscopy

41
Q

Very thin (__-___ nm),
resin-embedded tissue sections are typically studied by TEM
at magnifications up to approximately 120,000 times

A

40-90

42
Q

There are shades of gray region, black and white image.

A

TEM (Transmission Electron Microscopy)

43
Q

in TEM, if an electron passed readily it means?

A

electron lucent (brighter)

44
Q

in TEM, if electrons were absorbed or deflected

A

electron dense

45
Q
A