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INTRODUCTION TO DYNAMIC HISTOLOGY – ANAT 261



LABORATORY MANUAL



WRITTEN BY: CARLOS R. MORALES







INDEX







Electronic Slide Box …………………………………………………………….. Page 2



Lab 1 (Organization. Training. Skin and Epithelial tissue) ……………………… Page 3



Lab 2 (Skin and Annexes).………………………………………………………. Page 4



Lab 3 (Cartilage and Bone).……………………………………………………… Page 5



Lab 4 (Bone Formation) ………………………………………………………..... Page 6



Lab 5 (Muscle Tissue) …………………………………………………………… Page 7



Lab 6 (Blood Vessels) …………………………………………………………… Page 8



Lab 7 (Respiratory System).……………………………………………………… Page 9



Lab 8 (Oral Cavity).………………………………………………………………. Page 10



Lab 9 (Digestive Tract).…………………………………………………………… Page 11



Lab 10 (Associated Glands).…………………………………………….………… Page 12



Lab 11 (Urinary System) …………………………………………………….…… Page 13



Lab 12 (Nervous System) ………………………………………………………… Page 15









1

Electronic Slide Box





1. Skin - Finger

2. Striated Skeletal Muscle (Diaphragm)

3. Cardiac Muscle

4. Lip - Skin with hair follicles

5. Spinal Cord

6. Brain

7. Cerebellum

8. Tongue

9. Esophagus, Trachea, Elastic Arteries, Large Veins

10. Urinary Bladder

11. Lung

12 Submandibular Gland

13. Pancreas

14. Liver

15. Pyloric Stomach, Duodenum

16. Kidney

17. Mature and Developing Teeth

18. Sublingual Gland

19. Endochondral Bone Formation - Tendon

20. Endochondral Bone Formation

21. Compact Bone

22. Spinal Ganglion and Peripheral Nerve

23. Aorta

24. Rectum, Jejunum, Body of Stomach, Colon

25. Larynx (Elastic Cartilage)

26. Parotid Gland

27. Lung

28. Ileum

29. Ileum

30. Colon









2

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 1





Objectives





1. Organization: The teaching in the labs is organized as small group teaching. Six

or seven students are assigned to one station with a TA in charge of the group.

You will sit in the same station for the rest of the semester.

2. Learn the use of the Electronic Slide Box: Most of the activities described in this

manual specify the use of electronic slides. The electronic slides have been listed

separately (see Electronic Slide Box Document)

3. Learn the use of digitized micrographs: These micrographs are found in Images.

Generally, they will be used by the TA to demonstrate the lab activities, to answer

specific questions, and to review the lab. This folder also contains useful drawings

and electron microscope images. At the end you will find a section named

“cytology”. Feel free to use these electronic images in your assignment.

4. A Laboratory Review describing the main concepts that you should learn in the

lab is also available. Be advised to read the text prior to the lab.





Assignments





1. Become familiar with the laboratory systems: The use of the electronic slide box

will simulate light microscopy. At low power you will observe the image at a

0.4x. You can magnify the same field up to 40x which is equivalent to the high-

dry ocular of a light microscope. The small image at the corner has a red rectangle

that indicates the selected field. You can place it over the area you want to

observe. Additionally, the arrows at the bottom will allow you to move the picture

in different directions.

2. When using electronic slides, follow these steps of observation: A) Start with low

power (L.P) and end with high power (H.P.); B) What is a longitudinal, a cross

and an oblique section? C) Always identify your final magnification

3. Your TA may decide to show you first the Lab Images. In such a case use then the

electronic slide 1 for review. Identify the epidermis, dermis and hypodermis.





3

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 2





Objectives





1. To study the histology of the skin and its appendages (hair, sebaceous and sweat

glands).

2. To study the keratinized stratified squamous epithelium (epidermis).

3. To identify the phases of mitosis in the stratum germinativum (basal layer), i.e.,

interphase, prophase, metaphase, anaphase and telophase.

4. To identify the dermis and hypodermis.





Assignments





1. Use electronic slide 1. Make a drawing of the epidermis at L.P and H.P.

2. Use electronic slide 4. In the dermis, study the hair follicle and identify its layers

(C.T. sheath, glassy membrane, E.R.S., I.R.S., cuticle of hair shaft and cortex).

Use your Atlas of Histology and your drawings from the lecture. Note that the

I.R.S. is composed by the Henle’s layer, Huxley’s layer, and the cuticle of I.R.S.

3. Study the sebaceous gland at L.P. and H.P. Make a drawing.

4. Use slide 1. Study the sweat gland and its duct at L.P. and H.P.

5. Identify mitotic figures in the basal layer.

6. If you have time compare the epidermis to the dermis (C.T.) and hypodermis

(C.T.).





C.T.: connective tissue









4

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology

Laboratory 3





Objectives





1. To study the classification and histology of the connective tissue (using the

dermis and hypodermis as study models).

2. Histology of cartilage

3. Introduction to the histology of the bone.





Assignments





1. Use electronic slide 1. Study the dermis and hypodermis of the skin. The dermis

is divided into a papillary layer (loose connective tissue) and a reticular layer

(dense irregular connective tissue). The hypodermis is composed of adipose tissue

(a variety of loose connective tissue). Locate sweat glands and their ducts in

these layers of the skin.

2. Use electronic slide 9. Locate the trachea. Examine the hyaline cartilage. Study

the perichondrium, the isogenous groups and the extracellular matrix. Identify

chondroblasts and chondrocytes. In slide 25 find elastic cartilage. Identify elastic

fibers.

3. Use electronic slide 19 and locate dense regular C.T. (tendon). Note that the

collagen fibers run in one direction.

4. Slide 19. Note that the articular surface is made of hyaline cartilage. Do you see

perichondrium in this location?

5. Use electronic slide 21. Bone. Cross section of shaft (long, compact lamellar

bone). Identify the following structures: periosteum, outer circunferential system

or lamellae, Haversian system, inner circumferential system or lamellae,

endosteum, marrow, osteoblasts, osteocytes, osteoclasts, Haversian canals

(vascular canals).

6. Make drawings.









5

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 4





Objectives





1. To study the histology of the bone.

2. To study endochondral bone formation.





Assignments



1. Use slide 21. Review bone structure. Note the following points: Bone tissue is

made up of cells and matrix (matrix consists of collagen and ground substance).

The collagen is impregnated with minerals in the form of hydroxyapatite crystals.

2. Cells are: a- Osteoblasts (seen during bone formation) line the bone surfaces and

are large when active and flat when inactive. b- Osteocytes (lie in bone). They

are seen in small holes called lacunae. Osteocytes have processes which run in

small canaliculi in the bone matrix. c- Osteoclasts (bone resorption). These are

large multinucleated cells which remove bone (matrix, minerals and cells).

3. In the rat there are no true Haversian systems. But the canals containing blood

vessels may be considered to be Haversian canals. Review the following:

periosteum, endosteum, inner and outer circumferential systems and interstitial

system.

4. Study the articular surface (Slide 19, hyaline cartilage without perichondrium).

5. Slides 19 and 20. The bone that is first formed is embryonic or woven bone. This

bone is laid down around the cartilage model of the bone. The cartilage model is

removed during endochondral bone formation leaving two discs of cartilage at

either end of the bone; these are the epiphyseal plates. They are responsible for

the growth in length of the bones.

6. Slides 19 and 20. Study the epiphyseal plate. Identify the different layers (resting

cartilage, zone of proliferation, hypertrophy, cell death and mixed spicules.

6. Make drawings









6

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 5





Objectives





1. To study the histology of striated (skeletal) muscle.

2. To study the histology of cardiac muscle.

3. To study smooth muscle (wall of intestine).





Assignments





1. Use slides 2 and 8. Make drawings of longitudinal, cross and oblique sections of

muscle fibers (striated skeletal muscle). In cross sections identify peripheral

nuclei and myofibrils. In longitudinal sections note long multinucleated fibers,

peripheral nuclei and cross striations of the fiber.

2. Compare striated skeletal muscle to cardiac muscle (slide 3). Cardiac muscle is

similar to striated skeletal muscle, but has central nuclei and the fibers (cells) are

joined together at intercalated discs.

3. Compare striated skeletal muscle to smooth muscle (slides 15 and 24). Note

fibers in cross sections presenting centrally located nuclei. In longitudinal section

the fibers are elongated, spindle shaped with central nuclei.

4. Make drawings at L.P. and H.P.









7

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 6





Objectives





1. To study the histology of blood vessels (elastic arteries, muscular arteries,

arterioles, large veins, medium size veins and venules).

2. To identify the different layers of these vessels.





Assignments





1. Find a muscular artery (media with four or more layers of smooth muscle cells)

and a medium size vein in slides 1, 4, 8 and 24. In each case, try to identify cross

and longitudinal sections of blood vessels. Examine the intima, media and

adventitia. In the case of the arteries find the internal elastic limiting membrane

(IELM).

2. Identify other vessels such as arterioles and venules in the same sections. How do

they differ from muscular arteries and medium size veins?

3. Study elastic and large size veins. Use slides 9 and 27. Sketch a portion of the

media of the elastic artery showing fenestrated elastic membranes and the smooth

muscle fibers between them. What is and where is located the vasa vasorum?

4. Make drawings of all these vessels at L.P. and H.P.









8

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 7





Objectives

1. To study the histological organization of the trachea

2. To study the histology of the respiratory system





Assignments

1. Use slide 9. See that the lumen of the trachea is lined by a pseudostratified

columnar epithelium with cilia and goblet cells. Make a H.P. drawing. The thin

layer of connective tissue (loose) under the thickened basement membrane is the

lamina propria. This C.T. together with the epithelium is collectively called

mucosa. The connective tissue below the mucosa is the submucosa and contains

serous and mucous acini. Finally the submucosa merges with an open ring of

hyaline cartilage completely surrounded by perichondrium. Look from

chondrocytes (isogenic groups).

2. Find intrapulmonary bronchus (Slide 28). Study the folded mucosa, the

incomplete plates of cartilage and the presence of smooth muscle (Find slides in

the wooden box).

3. Slide 28. Find bronchioles (regular, terminal and respiratory), alveolar ducts,

alveolar sacs and alveoli. Identify macrophages and pneumocytes type II.

4. Make detailed drawings of these structures.









9

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 8





Objectives

1. To study the histology of the digestive system

a) Teeth

b) Tongue

c) Esophagus



Assignments





1. Teeth. Slide 17 (Cross section of monkey maxilla). Find erupted primary tooth

and unerupted permanent teeth. Examine the gingiva and the periodontal

ligament around the erupted tooth.

2. Study the gingiva. Find, if possible, the muco-gingival junction. Identify the

parakeratinized squamous epithelium.

3. Study the erupted tooth. Find the dentine and odontoblasts, the pulp, the

cementum and cementocytes. Find the Sharpey's fibers in the cementum. The

enamel (crown) is absent (removed during decalcification). What is different

about the cementum near the crown and at the tip of the root?

4. Developing crowns of permanent tooth. Find the enamel (white space and/or

bluish material), the ameloblasts (inner dental epithelium), stratum intermedium,

stellate reticulum, outer dental epithelium and Hertwig's epithelial root sheath.

What is the enamel organ?

5. Make drawings of all these structures. Also take a look at the inner aspect of the

lip (Slide 4).

6. Tongue (Slide 8). Find filiform, fungiform and circumvallate papillas. In the last

one, find the taste buds. Make drawings.

7. Esophagus (Slide 9). The mucosa consists of a non-keratinized stratified

squamous epithelium and a thin lamina propia (loose C.T.). There is a muscularis

mucosa. The submucosa is thick (dense C.T.) and contains mucous glands. The

tunica muscularis has two layers. The outermost layer is called adventitia. Make

drawings.

10

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 9





Objectives





1. Study of the histology and general organization of the gastro-intestinal tract

(esophagus, stomach and intestines).





Assignments

1. Review esophagus.

2. Reed on your atlas and lectures about the cardiac portion of the stomach (no

slides).



3. Body of the stomach. Slide 24. Find the mucosa and identify pits and glands.

The lamina propria is squeezed between the gastric glands. The gastric glands

extend down to the muscularis mucosa. Note the thin submucosa and the tunica

muscularis composed of three layers of smooth muscle. Sketch these layers under

L.P (10X). Identify the following cells: surface mucous cells, mucous neck cells,

parietal cells, zymogenic cells.

4. Pyloric portion of the stomach and duodenum. Slide 15. Follow the mucosa and

identify both regions. One follows the other. Note that in the pylorum, the glands

are lined by mucous cells. In the duodenum the mucosa forms villi and crypts.

The crypts are called crypts of Lieberkühn. In the epithelial lining (simple

columnar) identify enterocytes (columnar cells with brush border), goblet cells,

Paneth cells. Note the muscularis mucosa and beneath the submucosa containing

the Brünner's glands. Sketch these organs at L.P. and H.P.

5. Small intestine proper (Slides 24, 29 and 30). Identify the submucosa and

compare to the submucosa of the duodeneum. Slide 24: Note that this portion

corresponds to the jejunum; Why? Slides 29 and 30: Note that these images

correspond to the Ileum; Why? Make a drawing. Study the tunica muscularis.

What is the serosa? Make drawings.

6. Large intestine. (Slide 24, colon and rectum; Slide 31, colon). The mucosa

consists only of crypts of Lieberkühn. There are no villi. Sketch the mucosa.

Note the presence of many goblet cells and few striated border cells.



11

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology

Laboratory 10





Objectives

1. To study the histology of the glands associated with the digestive tract (salivary

glands, pancreas and liver).





Assignment





1. Salivary glands. Study the organization of compound glands in general. Note the

lobes subdivided into lobules. This subdivision is made by connective tissue as a

capsule with sub-partitions. Note the duct distribution as interlobar, interlobular,

and intralobular. Note that intralobular ducts are either intercalated or striated

ducts. a) Parotid Gland. Study in slide 26 the structure of the parotid gland. All

the acini are serous. Note that the intercalated ducts are short and that the striated

ducts are longer. b) Sublingual gland (slide 18). Most acini are mucous, usually

with serous demilunes. There are also a few serous acini. Study the duct system.

c) Submandibular gland: (slide 13). Most acini are serous, but there are some

patches of mucous acini.

2. Pancreas (slide 13). a) Exocrine pancreas. Study the serous acini which make up

most of the pancreas. They are typical serous glands with the addition of

centroacinar cell nuclei in their centers. The duct system of the pancreas consists

of long intercalated ducts (low cuboidal epithelium) emptying into small

intralobular ducts with cuboidal epithelium surrounded by a small amount of C.T.

These drain into larger interlobular ducts lined by a columnar epithelium and

surrounded by much C.T. Sketch these structures. b) Endocrine pancreas.

Constituted by small isolated islets of Langerhans surrounded by thin C.T. septa.

The cells within the islets are polyhedral and form cords around capillaries.

3. Liver (slide 14). Find the capsule of C.T. Identify the following structures: a) The

portal spaces containing a branch of the hepatic artery, portal vein and

interlobular bile duct. b) The central veins (center of the hepatic lobules). c) The

sinusoids and the cords of hepatocytes. Note that the sinusoids open into the

central vein. Identify the bile canaliculi between hepatocytes and the cholangioles

(small ducts linking the bile canaliculi with the interlobular ducts. Make sketches

of these structures.

12

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 11





Objectives

1. To study the histology of the kidney

2. To study the histology of the ureter and urinary bladder





Assignment





1. Kidney (Electronic Slide 16). L.P. observations: Find at the periphery of the

kidney the capsule and note the separation between the outer cortex and the inner

medulla (the cortex stains more intensely). In the cortex find branches of the

interlobular arteries which delimit the boundary of the lobules. The center of each

lobule usually has a straight medullary ray. H.P. observations: Find a renal

corpuscle and examine the parietal layer of Bowman's capsule, the glomerular

tufts of capillaries containing nuclei of endothelial cells, red blood cells,

mesangial cells, as well as the large light nuclei of podocytes (which correspond

to the visceral layer of Bowman's capsule). Draw a renal corpuscle at H.P.





Find other renal corpuscles which show: a) the junction with the proximal

convoluted tubule; b) the point of contact with a macula densa of the distal

convoluted tubule; c) the point of junction of the glomerular tuft with afferent

and efferent arterioles. Sketch each of these images.





Study the proximal convoluted tubules (which are more numerous than the distal).

The cells are cuboidal and deeply acidophilic and contain round central nuclei.

The lumen is smaller than that of the distal convoluted tubules and is partly

occluded by material. The apical border of the cells has a brush border. Make an

H.P. drawing of a section of this tubule.





Study the distal convoluted tubule. The cells are paler and smaller than in

proximal tubules. There is no brush border and the lumen is wider. The nuclei of

the cells are close to the apical plasma membrane. Draw a section of this tubule.





13

Study the medullary ray which is at the center of each lobule. The main duct in

the ray is the branched collecting tubule. The distal convoluted tubules drain into

it. The duct resembles the distal convoluted tubules, but the apices of the cells

seem to bulge into the lumen. The other tubules in the medullary ray are the

descending and ascending limbs of the loop of Henle. Identify the collecting

tubule, and make an sketch.





In the medulla identify the collecting tubules and the thin ad thick limbs of the

loop of Henle. Note the capillaries between the tubules; these can be confused

with the thin limbs of Henle's loop.





2. Histology of the ureter. It is a long muscular tube leading from the calyx of the

kidney to the urinary bladder. The lumen is star shaped in cross section and is

lined by transitional epithelium (Section 16 may or may not have a portion of this

organ). The lamina propria is elastic and merges with a submucosa, followed by

the muscle coat made up of 3 layers of smooth muscle (inner longitudinal, middle

circular and outer longitudinal). Find the beginning of the ureter at the hilum of

the kidney.





3. Histology of the urinary bladder (Slide 10). The bladder is a large muscular bag

for storing urine. It is lined by a transitional epithelium which is capable of great

distension. The smooth muscle coat is irregularly arranged in several layers.

Draw the transitional epithelium under H.P.









14

ANATOMY AND CELL BIOLOGY

Introduction to Dynamic Histology





Laboratory 12





Objectives





1. To study the histology of the nervous system





Assignment





1. Spinal ganglion cells (Electronic Slide 22). Study the histology of the spinal

ganglion and find the nerves emerging from it. The spinal ganglion consists of a

collection of the nerve cell bodies, nucleus plus perikaryon of the neurons. These

are the largest cells in the ganglion. The perikaryon is surrounded by a layer of

cuboidal satellite cells which are type of neuroglia. Study the cell body of a

neuron. The nucleus is round, large, located in the center and contains a large

nucleolus. The cytoplasm contains large flecks of basophilic material, Nissl

substance, which is the ergatoplasm (RER) of the cell. The Nissl substance

extends into the larger dendrites, but not into the axon hillock and/or axon. Some

neurons contain dark yellow pigment granules called lipofuscin granules.





Peripheral nerve. Leaving the ganglion is the posterior root of the spinal nerve, a

peripheral nerve containing nerve fibers (myelinated axons) of the neurons of the

spinal ganglion. Define the epineurium, perineurium and endoneurium. Axons

are slightly basophilic. The myelin sheath appears acidophilic and vacuolated.

The larger nuclei, with pale chromatin are the nuclei of Schwann cells. The

thinner, darker nuclei are fibrocytes of the endoneurium. Observe node of

Ranvier.





2. Cross section of spinal cord (Slide 22). Note the C.T. (pia mater) around the cord.

Outside the pia mater are sections of peripheral nerves (the anterior and posterior

roots of the spinal nerves). Distinguish the gray and white matter. The gray

matter is in the form of an H. It contains the cell bodies of neurons. The white

matter is on the outside and contains the nerve fibers running in the cord. Both

gray and white matter contains nuclei of neuroglial cells. In the center of the cord

15

is the central canal. It is lined by columnar cells, the ependymal cells. In the

anterior horn find the large neurons (anterior horn cells). Make drawings.





In the white matter there are nerve fibers, but the nuclei belong to three types of

neuroglia cells. The large pale nuclei are of astrocytes. The darker nuclei with a

distinctive nuclear membrane are the oligodendrocyte, and the smallest and

darkest nuclei, often irregular in shape are the microglia.





3. Study the section of the cerebellum (Slide 7). It is a sagital section through the

horizontal convolutions called lobes. Each has numerous secondary folding, each

being a folium. Study one cerebellar lobe; note the folia; find the core of the

white matter in the center of the lobe. Study the gray matter of the cortex. It

consists of three distinct layers. Next to the white matter is the granular layer,

containing numerous nuclei of small neurons. In the middle there is a single layer

of large cells with large dendritic processes extending into the outermost layer

called Purkinge cells. The outermost layer is the molecular layer and it is

composed of numerous neuronal processes and glial cell nuclei.





4. The cerebrum (Slide 6) shows some convolutions or folds. Identify again the

centrally located white matter and the gray matter on the outside. The cerebral

cortex of gray matter consists of poorly defined layers. An inner layer next to the

white matter, the polymorphic cell layer, consists of neurons of irregular and

variable size. In the middle pyramidal cell layer, the neurons tend to be shaped

like pyramids of differing size (some of these neurons have very large cell

bodies). The outermost layer is the molecular layer consisting of neuronal

processes and glial cells. Note that glial cells are also present in the outer cortical

layers. Also note that the vascular thin layer of C.T. on the outer surface of the

cerebrum is the pia mater and it is the innermost protective membrane for the

brain.









16



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