Lab 5C: Observe Animal Cells

Learning Objectives

After completing the lab, the student will be able to:

  1. Make wet mounts of bacteria, plant and animal cells and view them under the microscope;
  2. Observe and identify differences between cells and cell structures under low and high magnification and record your observations;
  3. Explain how and why microscope stains are used when viewing cells under the microscope.

Lab 5C:  Observing animal cells.

Introduction

Animal cells are eukaryotic and possess subcellular components in common with the plant cells you observed in Activity 2. Organelles that plant and animal cells share in common include the nucleus, Golgi apparatus, mitochondria, ribosomes, and the endoplasmic reticulum. These are all participants in protein synthesis. An illustration of an animal cell is shown in Figure 4.5. There are some exceptions to these general components. For example, mature red blood cells (RBC) which have ejected their nuclei to have more room for hemoglobin, the protein that carries oxygen around the body. One of the easiest eukaryotic cells to obtain in the lab is the squamous epithelial cell found in the tissue lining the internal surface of your cheek. These cells are arranged in a flat layer and are easy to remove and observe.

 

This illustration shows a typical eukaryotic animal cell, which is egg shaped. The fluid inside the cell is called the cytoplasm, and the cell is surrounded by a cell membrane. The nucleus takes up about one-half the width of the cell. Inside the nucleus is the chromatin, which is composed of DNA and associated proteins. A region of the chromatin is condensed into the nucleolus, a structure where ribosomes are synthesized. The nucleus is encased in a nuclear envelope, which is perforated by protein-lined pores that allow entry of material into the nucleus. The nucleus is surrounded by the rough and smooth endoplasmic reticulum, or ER. The smooth ER is the site of lipid synthesis. The rough ER has embedded ribosomes that give it a bumpy appearance. It synthesizes membrane and secretory proteins. In addition to the ER, many other organelles float inside the cytoplasm. These include the Golgi apparatus, which modifies proteins and lipids synthesized in the ER. The Golgi apparatus is made of layers of flat membranes. Mitochondria, which produce food for the cell, have an outer membrane and a highly folded inner membrane. Other, smaller organelles include peroxisomes that metabolize waste, lysosomes that digest food, and vacuoles. Ribosomes, responsible for protein synthesis, also float freely in the cytoplasm and are depicted as small dots. The last cellular component shown is the cytoskeleton, which has four different types of components: microfilaments, intermediate filaments, microtubules, and centrosomes. Microfilaments are fibrous proteins that line the cell membrane and make up the cellular cortex. Intermediate filaments are fibrous proteins that hold organelles in place. Microtubules form the mitotic spindle and maintain cell shape. Centrosomes are made of two tubular structures at right angles to one another. They form the microtubule-organizing center.
Figure 4.5: Diagram of the parts of an animal cell.

Safety Precautions

  • Wear gloves and lab coat to avoid spilling stain on yourself.
  • Be careful when handling glass slides; the edges may be sharp.
  • Dispose of used cover slips in a glass disposal box.
  • Observe proper use of the microscope; avoid handling the electric cord with wet hands.
  • Do not use the coarse adjustment knob of the microscope at 40x.
  • Inform your teacher immediately of any broken glassware as it could cause injuries.
  • Used cotton swabs are considered biohazard; dispose of swabs in the biohazard trash container as soon as you have used them.
  • Methylene blue is a dye; be cautious not to ingest methylene blue.

Materials:

  • Prepared slide of red blood cells
  • Light compound microscope
  • Clean microscope slide, cover slip
  • Clean cotton swab or toothpick
  • 0.5–1 percent methylene blue solution
  • Dropper or pipette
  • paper towels

For this activity, you will work in pairs.

Procedure

RED BLOOD CELLS (PREPARED SLIDE)

Step 1:  Examine the prepared slide labeled “Human Blood Smear.”  The red blood cells are the small circles that dominate the slide.  Their central pale areas (when present) are called their central pallor.  If you search you will find widely scattered, larger cells with multiple darker purplish internal features; these are white blood cells.

Step 2:  Estimate the average size of the red blood cells.  Will the technique(s) you used in the previous section for Elodea, Onion, and Potato cells work for these cells?  Why or why not?  Describe a procedure for use with the red blood cells.

Step 3:  Draw this slide at 4x, 10x, and 40x, including at least one white blood cell in the 40x.  Use arrows to label a red blood cell, a central pallor, and a white blood cell.

HUMAN MOUTH LINING (INSIDE CHEEK) CELLS

Step 1:   Prepare your cheek cell slides as shown in Figure 4.6 and Figure 4.7 and outlined below.

  • Take a clean cotton swab and gently scrape the inside of your mouth with a single stroke.
  • Smear the cotton swab or toothpick on the center of the microscope slide for 2 to 3 seconds.
  • Add a small drop of distilled water onto the smear, place your cover slip (not shown in drawing).
  • Place a small drop of methylene blue solution (a dye) on the edge of the cover slip, and wick it onto the smear by placing a dry paper towel on the opposite side, and drawing the water into it (which will pull in the stain from the other side).  Try to get as much of the stain to be dilute (vs. intense) blue as possible.
  • Remove any excess solution below or around the cover slip using a paper towel.
Prepare a cheek swab with step 1: remove epithelial cells from the inner cheek by rubbing a cotton swab against and, step 2: swirl the cotton swab onto a microscope slide.
Figure 4.6: How to prepare a cheek swab.
Staining a cheek epithelium slide with a drop of methylene blue dye on a slide.
Figure 4.7: How to stain cheek cells with methylene blue dye.

Step 2:  Hunt through the slide to find the “best” example of a cheek cell that you can (pale blue blob with a dark blue nucleus near the center).   How do you propose to estimate its size?   Describe a method.

Step 3:  Draw the view at 4x, 10x, and 40x, with your focal cell in the middle.  Label its outer cell membrane, cytoplasm, and nucleus.

 

Stained cheek cells under a microscope
Figure 4.8: Cheek cells stained with methylene blue dye.  Yours might be more spread apart.

Discussion

  1. Identify whether the following images (Figure 4.9a, Figure 4.9b, and Figure 4.9c) show an animal cell, a plant cell, or a prokaryote cell. Explain how you know the difference.
  2. Microscopic views of animal cell, a plant cell, or a prokaryote cell.
    Figure 4.9: This figure shows three photos of different cell types. The photo in part (a) shows green cells with smaller organelles within. The photo in part (b) shows numerous tiny oval-shaped cells. The photo in part (c) shows a complex arrangement of different types of cells, some with a nucleus.

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Lab Manual for Biology Part I (V2) Copyright © 2022 by LOUIS: The Louisiana Library Network is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, except where otherwise noted.

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