Histology and Embryology 组织学与胚胎学 Department of Histology and embryology Three Gorges...

Histology and Embryology

组织学与胚胎学Department of Histology and embryologyThree Gorges University, Yichang, China

Introduction

I.     What’s histology?

II.    Why we study it ?

III.  How to study it ?-Histological methods.

I. What’s histology?Histology (Greek words): /histo-tissue /logia-study of ,or knowledge of So, histology means the knowledge of tissue, is a b

ranch of Anatomy.Anatomy: ---gross anatomy ---microscopic anatomyStructures related to function. So, exactly, Histolog

y is a science which study the microstructure and the relationship between the structure and function of human being.

Cell: smallest unit of structure and function of body ↓tissue: group of cell+extracellular ground substance four basic tissue: ---epithelium ↓ ---connective tissue ---muscular tissue ---nervous tissueorgan: made up of tissue, have special shape, structu

re and function ↓system: organs Which have related function get togeth

er.

It is the bases of other subject in medicine.

It intertwines the disciplines of cell biology,

biochemistry, physiology, and as appropriate,

pathology. Students will recognize the

importance of this subject as they refer to the

text later in your careers.

II.What’s Embryology? Embryology is a kind of science which

study the processes and the regulations of the development of human fetus.

III.    How to study it- histological methods

---Development of histology deponds on the development of technique.

---Histology studies the microstructures. So, we should have the aid of microscope to study. Several types of microscopes are available. According to the light source used, microscopes can be basally classified as:

light microscope(LM) electron microscope(EM)

1. structure of Microscope

LM EM

---useful magnification: 1500X 800,000X

---resolution: 0.2um 0.2nm

2. Preparation of tissue for LMThe most routine one is paraffin section stained

with hematoxylin and eosin(H&E)The steps:a. Obtaining th specimen: fresh, small pieces (le

ss than 5 cubic milimeter(mm3))-tissue blockb. Fixation: fixatives: use formalin or Bouin’s to

preserve structural organisationc.  Dehydration: use ethyl alcohol to get rid of w

ater of tissue and cell

d.  Clearing: use xylene to get rid of alcohol

alcohol and xylene are embedding mediums

e.  Embedding: firstly, heat the paraffin, make it melt, then put tissue block into melted paraffin, allow paraffin harden, the tissue block is embedded in.

f.   Sectioning: use microtome to cut the tissue into 3-8um thick sections, then mounted them on glass slides

g.   H&E staining---Hematoxylin: basic stain, combines with acidi

c components, make them appear blue color- we call such components as basophilic

---Eosin: acidic stain, combines with basic components, make them appear pink color- we call such components as acidophilic(eosinophilic)

observing

3. Preparation of tissue for EM

The steps are same to preparation for LM

a.   tissue block: more small, less than 1mm3

b.   plastic materials for embedding

c. ultra-thin sections is about 30-50nm thick( use ultramicrotome)

d.   heavy metal salts- increase staining contrast

---lead citrate

---uranyl acetate

e. the beam of electron replace the light to illuminate the tissue sections

Beam of electron illuminate the tissue section, we use a screen to receive the electron. In some areas, the beam of electron is impeded by those tissue element which are stained with heavy metal salts, so very few electrons penetrate to excite the screen, such areas appear dark, are described as electron-dense areas. Unstained areas, by contrast, appear light, we call them as electron-lucent areas.

4. Histochemistry1)    General Histochemistry: Combine histological methods with chemical

or biochemical methods, make some compositions of tissue or cell become insoluble, colored or electron-dense,, to show those chemical compositions of tissue or cell in situ, such compositions includes protein,amino acid, nucleic acid, lipid and enzymes.

*Periodic acid schiff reaction(PAS reaction): schiff’s reagent (colorless)

Polysaccharides → aldehydes → magenta complexes

Glycogen oxidize combine (purple red colored)

2) immnohistochemistry: antigen-antibody

3) in situ hybridization: nucleic acid: DNA(desoxyribose nucleic acid) RNA(ribose nucleic acid)