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16 Key Cell Types and Tissues in the Human Body

In this section

The most common cell shapes in the human body are squamous (flat), cuboidal (cube-like) and columnar (column-like) and these join together to form tissues that can act as barriers, aid signalling and nutrient and gas transfer and also some can confer protection to underlying tissues or organs. The tissues of multicellular, complex animals can be categorised into four primary types: epithelial, connective, muscle and nervous. Each of these tissues have cells that have a specific role to aid in the functioning of the tissue and in the organs. Each cell has a particular orientation (basal side and apical or free side) and normal cells have a uniform shape, size, function and appearance at a specific location and if changes occur to this appearance and function this can indicate pathology, such as cancer.

Epithelial Tissues

Epithelial tissues cover the outside of organs and structures in the body and line the lumens of organs in a single layer or multiple layers of cells. Epithelial cells fit together tightly to support their protective role in the body. This is accomplished as cells are attached to a basement membrane and each cell is connected to the adjacent cells by special attachments (junctions) which can also aid in cell communication (Figure 5.1).

 

Diagram of three basic types of cell-to-cell junctions are tight junctions, gap junctions, and anchoring junctions.
Figure 5.1. Types of Cell Junctions: The three basic types of cell-to-cell junctions are tight junctions, gap junctions, and anchoring junctions. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

The types of epithelia are classified by the shapes of cells present and the number of layers of cells. Epithelia composed of a single layer of cells attached to a basement membrane is called simple epithelia whereas epithelial tissue composed of multiple layers is called stratified epithelia. Naming of the type of epithelia takes into account the number of cell layers and the cell shape on the free (apical) edge eg a stratified squamous epithelia would have two or more cell layers with squamous cells on the apical (free) surface (Figure 5.2). This architecture also reflects their role/function and location (Table 5.1).

 

Simple epithelial tissue is organized as a single layer of cells and stratified epithelial tissue is formed by several layers of cells.
Figure 5.2. Cells of Epithelial Tissue: Simple epithelial tissue is organised as a single layer of cells and stratified epithelial tissue is formed by several layers of cells. Source: Image created and adapted by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

 

Table 5.1 Types of Epithelial Tissues

Cell shape Description Location Role/function examples
squamous flat, irregular, slightly rounded shape simple: lung alveoli, capillaries; stratified: skin, mouth, vagina gas exchange in lung alveoli (simple squamous)
cuboidal cube shaped, central nucleus glands, renal tubules secretion and absorption in liver and kidneys
columnar tall, narrow, nucleus toward base; tall, narrow, nucleus along cell simple: digestive tract; pseudostratified: respiratory tract secretion and absorption in gastrointestinal tract
transitional round, simple but appear stratified urinary bladder alows expansion

Squamous Epithelia

Squamous epithelial cells are generally round, flat and have a small, centrally located nucleus. The cell outline is slightly irregular and cells fit together to form a covering or lining. When the cells are arranged in a single layer on a basement membrane (simple epithelia), they facilitate diffusion in tissues, such as the areas of gas exchange in the lungs and the exchange of nutrients and waste at blood capillaries. When the cells are arranged in multiple layers (stratified epithelia), they form a thicker layer generally used for protection, such as in the skin and in tissues lining the mouth and vagina, where abrasion and damage may occur (i.e. outer cells can be lost but inner cells and membranes are still protected). The human cervix photomicrograph (Figure 5.3b) shows a stratified, squamous epithelium (many layers of cells with squamous cells on the free surface).

 

Squamous epithelia cells (a) have a slightly irregular shape, and a small, centrally located nucleus. These cells can be stratified into layers, as in (b) this human cervix specimen
Figure 5.3. Squamous epithelia cells (a) have a slightly irregular shape, and a small, centrally located nucleus. These cells can be stratified into layers, as in (b) this human cervix specimen. Source: (a) Image by Rice University, OpenStax is licensed under a CC BY 4.0 licence.; (b) Image by Dr Ed Uthman, is licensed under a CC BY 4.0 licence, scale-bar data from Matt Russell and adapted by Rice University, OpenStax and licensed under a CC BY 4.0 licence.
Simple cuboidal epithelial cells line tubules in the mammalian kidney, where they are involved in absorbing substances from filtrate produced in the kidney.
Figure 5.4. Simple cuboidal epithelial cells line tubules in the mammalian kidney, where they are involved in absorbing substances from filtrate produced in the kidney. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Cuboidal Epithelia

Cuboidal epithelialcells (Figure 5.4), are cube-shaped with a single, central nucleus. They are most commonly found in a single layer (a simple epithelia) and are involved in secretion and absorption depending on the location and need of the cells or tissues. Cuboidal epithelial cells are located in glandular tissues throughout the body, producing and secreting substances such as mucus and digestive juices. These cell types are also found in the walls of tubules and in the ducts of the kidney and liver and play key roles in both secretion and absorption.

Columnar Epithelia

Columnar epithelial cells are taller than they are wide (like a column) and are mostly found as a simple, columnar epithelia with an elongated nucleus located in the basal end of the cell (near the basement membrane; Figure 5.5). This type of epithelia is mostly located in the digestive tract, with the apical surfaces having invaginations (for secretion) and finger-like projections (villi and microvilli) for absorption. Villi and microvilli on the apical surface increase surface area for absorption and therefore increase absorption efficiency of materials from the lumen of the digestive tract then cell prepares it for entry into the body through the circulatory and lymphatic systems. Simple columnar epithelia also line parts of the female reproductive tract and in this location, the apical surface is modified with cilia that beat in unison to aid in the movement of the ovum towards the uterus. Ciliated, columnar epithelia are also found in the respiratory system to help move particulate matter (eg dust particles etc) away from the lungs. Goblet cells (Figure 5.6) are interspersed in some tissues (such as the lining of the trachea). The goblet cells contain mucus that traps irritants, which in the case of the trachea keep these irritants from getting into the lungs.

Simple columnar epithelial cells absorb material from the digestive tract. Goblet cells secrete mucus into the digestive tract lumen. Some columnar epithelial cells lining the respiratory tract appear to be stratified. However, each cell is attached to the base membrane of the tissue and therefore, they are simple epithelia. The nuclei are arranged at different levels in the layer of cells, making it appear as though there is more than one layer
Figure 5.5. Simple columnar epithelial cells absorb material from the digestive tract. Goblet cells secrete mucus into the digestive tract lumen. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

 

Pseudostratified columnar epithelia line the respiratory tract.
Figure 5.6. Some columnar epithelial cells lining the respiratory tract appear to be stratified. However, each cell is attached to the base membrane of the tissue and therefore, they are simple epithelia. The nuclei are arranged at different levels in the layer of cells, making it appear as though there is more than one layer. This is called pseudostratified, columnar epithelia. Pseudostratified columnar epithelia line the respiratory tract. They exist in one layer, but the arrangement of nuclei at different levels makes it appear that there is more than one layer. Goblet cells interspersed between the columnar epithelial cells secrete mucus into the respiratory tract. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Transitional Epithelia

Transitional or uroepithelial cells appear only in the urinary system, primarily in the bladder and ureter. These cells are arranged in a stratified layer, but they have the capability of appearing to pile up on top of each other in a relaxed, empty bladder (Figure 5.8). As the urinary bladder fills, the epithelial layer unfolds and expands to hold the volume of urine introduced into it. As the bladder fills, it expands, and the lining becomes thinner – meaning, the tissue transitions from thick to thin.

Transitional epithelia of the urinary bladder
Figure 5.7. Transitional epithelia of the urinary bladder undergo changes in thickness depending on how full the bladder is. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Connective Tissue

Connective tissues are made up of a matrix consisting of living cells and a nonliving substance, called the ground substance. The ground substance is made of organic substances (usually protein, such as proteoglycan) and an inorganic substance (usually a mineral or water), typically giving a gel-like consistency (with exceptions). The principal cell of connective tissues is the fibroblast. This cell makes the fibres found in nearly all connective tissues. Fibroblasts are motile, able to carry out mitosis and can synthesise whichever connective tissue is needed at that location. Macrophages, lymphocytes and occasionally, leukocytes can be found in some of the tissues. Some tissues have specialised cells that are not found in the others. The matrix in connective tissues gives the tissue its density.

The organic portion or protein fibres found in connective tissues are either collagen, elastic or reticular fibres. Collagen fibres provide strength to the tissue, preventing it from being torn or separated from the surrounding tissues. Elastic fibres are made of the protein elastin; this fibre can stretch to one and one half of its length and return to its original size and shape. Elastic fibres provide flexibility to the tissues. Reticular fibres are the third type of protein fibre found in connective tissues. This fibre consists of thin strands of collagen that form a network of fibres to support the tissue and other organs to which it is connected. There are various types/forms of connective tissue, the types of cells and fibres they are made of, and sample locations of the tissues (Table 5.2).

Table 5.2. Types of connective tissues

Tissue Cells Fibres Location
loose/areolar fibroblasts, macrophages, some lymphocytes, some neutrophiles few: collagen, elastic, reticular around blood vessels; anchors epithelia
dense, fibrous connective tissue fibroblasts, macrophages mostly collagen irregular: skin regular: tendons, ligaments
cartilage chondrocytes, chondroblasts hyaline: few collagen fibroicartilage: large amount of collagen shark skeleton, foetal bones, human ears, intervertebral discs
bone osteoblasts, osteocytes, osteoclasts some: collagen, elastic vertebrate skeletons
adipose adipocytes few: collagen, elastic, reticular adipose (fat)
blood red blood cells, white blood cells none blood

Loose/Areolar Connective Tissue

Loose connective tissue, also called areolar connective tissue, has a sampling of all components of a connective tissue with some fibroblasts together with leukocytes including macrophages, lymphocytes and neutrophils (Figure 5.7). The collagen fibres present are relatively wide and stain a light pink, while elastic fibres are thin and stain dark blue to black. The space between the formed elements of the tissue is filled with the matrix. The material in the connective tissue gives it a loose consistency like a cotton ball that has been pulled apart. Loose connective tissue is found around every blood vessel and helps to keep the vessel in place. The tissue is also found around and between most body organs. In summary, areolar tissue is tough, yet flexible and comprises membranes.

 

Loose connective tissue composed of loosely woven collagen and elastic fibres
Figure 5.8. Loose connective tissue is composed of loosely woven collagen and elastic fibres. The fibres and other components of the connective tissue matrix are secreted by fibroblasts. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Fibrous Connective Tissue

Fibrous connective tissues contain large amounts of collagen fibres and few cells or matrix material. The fibres can be arranged irregularly or regularly with the strands lined up in parallel. Irregularly arranged fibrous connective tissues are found in areas of the body where stress occurs from all directions, such as the dermis of the skin. Regular fibrous connective tissue (Figure 5.9), is found in tendons (which connect muscles to bones) and ligaments (which connect bones to bones) and due to the dense packing of these fibres in parallel, this gives good resistance to forces along one axis but also allows for a bit of stretch.

 

egular fibrous connective tissue from the tendon has strands of collagen fibres lined up in parallel.
Figure 5.9. Regular fibrous connective tissue from the tendon has strands of collagen fibres lined up in parallel. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Cartilage

Cartilage is a connective tissue with a large amount of the matrix and variable amounts of fibres. The cells, called chondrocytes, make the matrix and fibres of the tissue. Chondrocytes are found in spaces within the tissue called lacunae.

A cartilage with few collagen and elastic fibres is hyaline cartilage (Figure 5.10). The lacunae are randomly scattered throughout the tissue and the matrix takes on a milky or scrubbed appearance with routine histological stains. Sharks have cartilaginous skeletons, as does nearly the entire human skeleton during a specific pre-birth developmental stage. A remnant of this cartilage persists in the outer portion of the human nose. Hyaline cartilage is also found at the ends of long bones, reducing friction and cushioning the articulations of these bones.

 

Hyaline cartilage
Figure 5.10. Hyaline cartilage consists of a matrix with cells called chondrocytes embedded in it. The chondrocytes exist in cavities in the matrix called lacunae. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Elastic cartilage has a large number of elastic fibres, giving it tremendous flexibility. The ears of most vertebrate animals contain this cartilage as do portions of the larynx, or voice box. Fibrocartilage contains a large amount of collagen fibres, giving the tissue tremendous strength. Fibrocartilage comprises the intervertebral discs in vertebrate animals. Hyaline cartilage found in movable joints such as the knee and shoulder becomes damaged because of age or trauma. Damaged hyaline cartilage is replaced by fibrocartilage and results in the joints becoming “stiff.”

Bone

Bone, or osseous tissue, is a connective tissue that has a large amount of two distinct types of matrix material. The organic matrix is like the matrix material found in other connective tissues, including some amount of collagen and elastic fibres. This gives strength and flexibility to the tissue. The inorganic matrix consists of mineral salts—mostly calcium salts—that give the tissue hardness. Without adequate organic material in the matrix, the tissue breaks; without adequate inorganic material in the matrix, the tissue bends.

There are three types of cells in bone: osteoblasts, osteocytes, and osteoclasts. Osteoblasts are active in making bone for growth and remodelling. Osteoblasts deposit bone material into the matrix and, after the matrix surrounds them, they continue to live, but in a reduced metabolic state as osteocytes. Osteocytes are found in lacunae of the bone. Osteoclasts are active in breaking down bone for bone remodelling, and they provide access to calcium stored in tissues. Osteoclasts are usually found on the surface of the tissue.

Bone can be divided into two types: compact and spongy. Compact bone is found in the shaft (or diaphysis) of a long bone and the surface of the flat bones, while spongy bone is found in the end (or epiphysis) of a long bone. Compact bone is organised into subunits called osteons (Figure 5.11). A blood vessel and a nerve are found in the centre of the structure within the Haversian canal, with radiating circles of lacunae around it known as lamellae. The wavy lines seen between the lacunae are microchannels called canaliculi; they connect the lacunae to aid diffusion between the cells. Spongy bone is made of tiny plates called trabeculae; these plates serve as struts to give the spongy bone strength. Over time, these plates can break causing the bone to become less resilient. Bone tissue forms the internal skeleton of vertebrate animals, providing structure to the animal and points of attachment for tendons.

 

(a) Compact bone is a dense matrix on the outer surface of bone. Spongy bone, inside the compact bone, is porous with web-like trabeculae. (b) Compact bone is organised into rings called osteons. Blood vessels, nerves, and lymphatic vessels are found in the central Haversian canal. Rings of lamellae surround the Haversian canal. Between the lamellae are cavities called lacunae. Canaliculi are microchannels connecting the lacunae together. (c) Osteoblasts surround the exterior of the bone. Osteoclasts bore tunnels into the bone and osteocytes are found in the lacunae.
Figure 5.11. (a) Compact bone is a dense matrix on the outer surface of bone. Spongy bone, inside the compact bone, is porous with web-like trabeculae. (b) Compact bone is organised into rings called osteons. Blood vessels, nerves, and lymphatic vessels are found in the central Haversian canal. Rings of lamellae surround the Haversian canal. Between the lamellae are cavities called lacunae. Canaliculi are microchannels connecting the lacunae together. (c) Osteoblasts surround the exterior of the bone. Osteoclasts bore tunnels into the bone and osteocytes are found in the lacunae. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Adipose

Adipose tissue, or fat tissue, is considered a connective tissue even though it does not have fibroblasts or a real matrix and only has a few fibres. Adipose tissue is made up of cells called adipocytes that collect and store fat in the form of triglycerides, for energy metabolism and also produce a number of growth factors and hormones. Adipose tissues additionally serve as insulation to help maintain body temperatures, allowing animals to be endothermic and they function as cushioning against damage to body organs. Under a microscope, adipose tissue cells appear empty due to the extraction of fat during the processing of the material for viewing (Figure 5.12). The thin lines in the image are the cell membranes and the nuclei are the small, black dots at the edges of the cells.

 

Adipocytes
Figure 5.12. Adipose is a connective tissue is made up of cells called adipocytes. Adipocytes have small nuclei localised at the cell edge. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Blood

Blood is considered a connective tissue because it contains living cells in a matrix (Figure 5.13). The living cell types are erythrocytes (red blood cells (RBC)), and leukocytes (white blood cells (WBC)). The fluid portion of whole blood, its matrix, is commonly called plasma.

 

Diagram of blood
Figure 5.13. Blood is a connective tissue that has a fluid matrix (plasma) and no fibres. Erythrocytes (red blood cells), the predominant cell type, are involved in the transport of oxygen and carbon dioxide. Also present are various leukocytes (white blood cells) involved in immune response. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

The cell type found in greatest abundance in blood is the erythrocyte. Erythrocytes are consistently the same size in a species but vary in size between species. Mammalian erythrocytes lose their nuclei and mitochondria when they are released from the bone marrow where they are made, whereas fish, amphibian and avian red blood cells maintain their nuclei and mitochondria throughout the cell’s life. The principal job of an erythrocyte is to carry and deliver oxygen to the tissues which is done in all species.

Leukocytes are the white blood cells found in the peripheral blood, with a number of different types with different roles. Lymphocytes function primarily in the immune response to foreign antigens or material. Different types of lymphocytes make antibodies tailored to the foreign antigens and control the production of those antibodies. Neutrophils are phagocytic cells and they participate in one of the early lines of defence against microbial invaders, aiding in the removal of bacteria that has entered the body. Another leukocyte that is found in the peripheral blood is the monocyte. Monocytes give rise to phagocytic macrophages that ‘clean up’ (phagocytose) dead and damaged cells in the body, whether they are foreign or from the host animal. Two additional leukocytes in the blood are eosinophils and basophils — both help to facilitate the inflammatory response.

Platelets or thrombocytes are fragments of a cell made in the bone marrow. Platelets participate in the stages leading up to coagulation of the blood to stop bleeding through damaged blood vessels. Blood has a number of functions, but primarily it transports material through the body to bring nutrients to cells and remove waste material from them while also providing immune functions.

Muscle Tissues

There are three types of muscle in animal bodies: smooth, skeletal and cardiac. They differ by the presence or absence of striations or bands, the number and location of nuclei, whether they are voluntarily or involuntarily controlled and their location within the body (Table 5.3).

Table 5.3. Muscle characteristics

Type of Muscle Striations Nuclei Control Location
cardiac yes single, in centre involuntary heart
skeletal yes many, at periphery voluntary skeletal muscles
smooth no single, in centre involuntary visceral organs

Cardiac Muscle

Diagram of cardiac muscles, skeletal muscles and smooth muscles
Figure 5.14. Cardiac muscle cells have striations, but, unlike the multinucleate skeletal cells, they have only one nucleus. Cardiac muscle tissue also has intercalated discs, specialised regions running along the plasma membrane that join adjacent cardiac muscle cells and assist in passing an electrical impulse from cell to cell. Smooth muscle cells do not have striations, while skeletal muscle cells do. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

Cardiac muscle (Figure 5.14), is found only in the heart. Like skeletal muscle, it has cross striations in its cells, but cardiac muscle has a single, centrally located nucleus. Cardiac muscle is not under voluntary control but can be influenced by the autonomic nervous system to speed up or slow down. An added feature to cardiac muscle cells is a line than extends along the end of the cell as it abuts the next cardiac cell in the row. This line is called an intercalated disc: it assists in passing electrical impulse efficiently from one cell to the next and maintains the strong connection between neighbouring cardiac cells.

Skeletal Muscle

Skeletal muscle (Figure 5.14), has striations across its cells caused by the arrangement of the contractile proteins, actin and myosin. These muscle cells are relatively long and have multiple nuclei along the edge of the cell. Skeletal muscle is under voluntary, somatic nervous system control and is found in the muscles that move bones.

Smooth Muscle

Smooth muscle (Figure 5.14), does not have striations in its cells. It has a single, centrally located nucleus. Constriction of smooth muscle occurs under involuntary, autonomic nervous control and in response to local conditions in the tissues. Smooth muscle tissue is also called non-striated as it lacks the banded appearance of skeletal and cardiac muscle. The walls of blood vessels, the tubes of the digestive system and the tubes of the reproductive systems are composed of mostly smooth muscle.

Nervous Tissue

Nervous tissues are made of cells specialised to receive and transmit electrical impulses from specific areas of the body and to send them to specific locations in the body. The main cell of the nervous system is the neuron (Figure 5.15). The large structure with a central nucleus is the cell body of the neuron. Projections from the cell body are either dendrites specialised in receiving input or a single axon specialised in transmitting impulses.

Glial cells (neuroglial cells or glia) are sometimes included in nervous tissue definitions, however they are more of a ‘supportive’ cell type and do not directly engage in electrical signalling but support neurons to carry out this role. There are three distinct types of glial cells: astrocytes (which regulate the chemical environment of the nerve cell); oligodendrocytes (which insulate the axon with myelin sheaths so the electrical nerve impulse is transferred more efficiently) and microglial cells (which are clear cell debris).

 

The neuron has projections called dendrites that receive signals and projections called axons that send signals. Also shown are two of the types of glial cells: astrocytes regulate the chemical environment of the nerve cell and oligodendrocytes insulate the axon so the electrical nerve impulse is transferred more efficiently.
Figure 5.15. The neuron has projections called dendrites that receive signals and projections called axons that send signals. Also shown are two of the types of glial cells: astrocytes regulate the chemical environment of the nerve cell and oligodendrocytes insulate the axon so the electrical nerve impulse is transferred more efficiently. Source: Image by Rice University, OpenStax, licensed under a CC BY 4.0 licence.

 

 

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