LAB03- Thin Smear of Peripheral Blood & RBC Counting

First Year Lab Number 03 for BS/MS students at IISER Pune

26-30 Aug 2013 in PEB3 Bio-Labs, IISER Pune.

Conducted by:

Dr. Chaitanya Athale,

Dr. Gayathri Pananghat,

Dr. Krishanpal Karmodiya,

Dr. Jayeeta Banerjee and

Dr. Shital Ahale

with inputs from Ashwini Keskar and Dr. Neelesh Dahanukar.

Click here to download the PROTOCOL

The most interesting images taken by students will be uploaded, if you send them (with your name and batch) to the coordinator of this module Chaitanya Athale (c a th a le at the rate of i i s er pune etc)

Fig 1: A collage of Arthropods. Copyright Wikipedia.

The colour of blood

Subphylum: Vertebrata has a Fe3-centred Hemoglobin: Red when oxygenated.

Phylum Arthropoda: Cu-centred Hemocyanin: Blue when oxygenated. Not all Arthropods show this, for example those belonging to Class Insecta.

Red blood from a grouper fish compared to blue blood from a mollusc

Fig 2: Red blood compared to blue blood (Copyright: Stanford University's Hopkins Marine Station, Pacific Grove, CA, USA).

Hematopoesis

Thigh bone in adult humans contains bone marrow which gives rise to the different lineages of the blood cells found in circulation.

Blood transfusion and Storage

1914: Albert Hustin & Luis Agote demonstrated Sodium Citrate (Na₃C₆H₅O₇) as anticoagulant for blood transfusions

Used at concentrations of 3.2% w/v in H₂O

Sodium citrate is a mild irritant

First Recorded Blood Storage

Blood bank: 1935 Dr John S. Lundy, Mayo Clinic, USA.

Citrated blood with glucose stored in an “ice box” for 14 days

Patients given citrated blood helped recovery

Blood Bank Tests

Central Drugs Standards Control Org., Govt of India

Hepatitis B virus (HBV)

Hepatitis C virus (HCV 3.0)

Human Immunodeficiency viruses, Types 1 and 2 (HIV 1,2)

Human T-Lymphotropic virus (HTLV-I/II)

Syphilis (Treponema pallidum)

Anti-Plasmodium antibody

Thin Smear of Blood

Peripheral blood (capillary)

Allows identification of blood types

Blood pathogens

Qualitative measure of infection & inflammation by microscopic examination

Relative proportion of blood cells

Basic and gold standard test in diagnostics

Can be preserved

Cheap and easy to do

1. Making a Thin Smear

Label the slide with your name

Clean with a tissue paper to remove grease, industrial coating

Hold the slides only from the edges

Place on a piece of kitchen towel

Unsheath the lancet from protective pack

Swab the finger to be pricked with using 70% Ethanol which has been soaked in piece of cotton (middle or ring-finger)

2. Smear the Blood Droplet

Smearing the blood droplet- a schematic view

Fig 4: Spreading the blood droplet

3. Discarding Lancet and Swab

Place lancet after use in its original paper cover, and bend it in the middle to ensure no re-use is done

Discard lancet and swab ONLY in designated containers

Use two swabs one before puncturing and one after

4. Fixation & Stain

Air dry (do not heat) blood smear

Dip 10 s in 99% methanol, let it drip dry

Dip 15 min in concentrated Giemsa stain, let it drip dry

Rinse in water, let it drip dry

Observe under a microscope 10x, 40x (air)

5. Clean up

Discard material only in appropriate containers

Clean working area with bleach (or ethanol)

Artefacts in RBC Morphology

Water artifact: humidity or water in fixative

Crenation: due to slow drying

Smudged cells: blood aging

Stains

Leishman Stain (Leishman 1901)

Methylene blue: Basic dye for acidic material (e.g. nucleic acids- DNA, RNA). Colour bluish-purple

Eosin-Y: Acidic dye for basic material. Pinkish colour, usually cytoplasmic

Wright-Giemsa Stain (Wright 1902, Giemsa 1904)

Methylene blue: Basic dye for acidic material (e.g. nucleic acids- DNA, RNA)

Azure B: Basic dye for acidic material (e.g. nucleic acids- DNA, RNA)

Eosin-Y: Acidic dye for basic material. Colour pinkish colour, usually cytoplasmic

To Do

Observe different blood cell types

Note and describe colour and morphology as you see

How many morphologically different cell types do you observe? Draw a schematic figure for each.

Differential count: WBCs to RBCs in a given field of view. Compare to textbooks.

Platelets

Typically 0.3 times the number of RBCs

Prevent bleeding by aggregation in response to injury

Release potent chemotactic factors to aid wound healing

Originate from megakaryocytes

Comparing Sizes

Ultrastructural image in scanning electron microscope (SEM)

White Blood Cell (WBC) Types


	Neutrophil (polymorpho nuclear leukocytes)	Basophils	Eosinophils (Granulocytes)	Monocytes	Lymphocytes

Percentage of total WBCs	40-50%	0.5-1%	1-4%	2-8%	20-40%

Red Blood Cell Count

RBCs do not require staining due to pigmentation. Using citrated-blood the count of RBCs can be made in a calibrated hemocytometer.

High cell densities mean dilution required. Using a Red Blood Cell Dilution pipette we take in 0.5 times volume into the pipette of a lancet-pricked blood droplet. The volume units are arbitrarily selected and the proportionate gradations of 0.1 indicate progression upto 0.5. The remaining pipette volume is made upto 101 (marked beyond the bulb) with 3.2% Sodium Citrate.

Hemocytometer

A calibrated chamber with grids (XY) and a heavy cover-slip to maintain constant height (Z)- volume constant. The RBC counting region consists of 25 boxes (5x5) bounded by either bold lines (see below left) or triple-lines.

How to count

Count in each 4x4 box (figure above, right) the SUM OF RBCs

Use L-rule for cells falling on bounding boxes (vertical line in right box, horizontal line in upper box)

Report your values on the board

Use the mean of 25 boxes for a blood cell count per microlitre

What is the error in counting likely to be? How will you calculate the error? What are the sources of this error?

Your Submissions


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