Bronchial Anatomy

Updated: Nov 26, 2024
  • Author: Angel Rolando Peralta, MD; Chief Editor: Vinay K Kapoor, MBBS, MS, FRCSEd, FICS, FAMS  more...
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Overview

Overview

The tracheobronchial tree is the anatomical and functional segment of the respiratory system that conducts air from the upper airways to the lung parenchyma. It is composed of the trachea and the intrapulmonary airways, including the bronchi (from the Greek bronkhos, meaning "windpipe"), bronchioles, and respiratory bronchioles. Different histological characteristics are seen at each level and serve specific purposes. [1, 2, 3]

  • Trachea and bronchi - The walls are supported by C-shaped rings of hyaline cartilage that maintain airway patency. The epithelium is pseudostratified ciliated columnar with goblet cells that produce mucus to trap particles. [4]
  • Bronchioles - These smaller airways lack cartilage but are surrounded by smooth muscle, allowing airflow regulation. The epithelium transitions to simple cuboidal cells, with fewer goblet cells. [4]
  • Respiratory bronchioles - These mark the transition from purely conducting airways to those involved in gas exchange. They contain alveoli along their walls, allowing for some gas exchange. [4]
  • Alveoli - The terminal units of the respiratory tree are lined with type I pneumocytes for gas exchange and type II pneumocytes for surfactant production, which reduces surface tension. [4]

The tracheobronchial tree undergoes approximately 23 generations of branching, from larger airways (trachea and primary bronchi) to smaller conducting airways (bronchioles), finally terminating in the alveoli, where oxygen diffuses into blood and carbon dioxide is removed. The branching pattern is asymmetrical but optimized for efficient airflow distribution and gas exchange. Asymmetry ensures uniform ventilation across lung regions. [4, 5]

The trachea (generation 0) serves as the central "trunk" of this tree-like structure, extending from the larynx (at the level of the body of the sixth (in females) or seventh (in males) cervical vertebra) to the carina, where it divides into the right and left main bronchi. The right main bronchus is shorter, wider, and more vertically oriented than the left, which is longer and more horizontal due to the position of the heart. Each main bronchus further branches into lobar (secondary) bronchi, corresponding to the lobes of each lung (three on the right and two on the left). These then divide into segmental (tertiary) bronchi, which supply specific bronchopulmonary segments. These segments are pyramidal in shape and independently supplied by their own segmental bronchus and pulmonary artery branch. [4, 6]

The tracheobronchial tree not only conducts air but also filters, warms, and humidifies it before it reaches the delicate alveolar surfaces. The mucus produced by goblet cells traps particulates, while ciliary motion propels it upward toward the pharynx for clearance. [4, 5]

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Gross Anatomy

The trachea is the segment that connects the upper airways to the bronchi. It has 16-22 cartilaginous rings in the anterior and lateral walls (cartilaginous portion) and a thin band of smooth muscle in the posterior wall (membranous portion). This configuration supports the tracheal anatomy during inspiration and expiration. [7]

The trachea extends distally 10-12 cm and divides into the right and left mainstem bronchi (primary) at the level of the body of the fifth or sixth thoracic vertebra (see image below). 

The right mainstem bronchus originates higher than the left mainstem bronchus; it is also shorter, wider, and more vertical. It measures about 2.5 cm and appears as a direct continuation of the trachea. The left mainstem bronchus is about 5 cm in length.

Mainstem bronchi divide into lobar bronchi (secondary) and subsequently into segmental (tertiary) bronchi (see the image below). Arteries, veins, and lymphatics also enter the lungs at the hilum along with the bronchi. A bronchopulmonary segment is a portion of the lung that is supplied by a segmental bronchus and its adjacent blood vessels.

Bronchi, anterior view. Bronchi, anterior view.

The right mainstem bronchus divides into the right upper lobe bronchus and the bronchus intermedius (BI). The former then divides into three segments: apical (RB1), posterior, (RB2), and anterior (RB3). The bronchus intermedius divides into the right middle lobe and right lower lobe bronchi. The right middle lobe bronchus has two segments: lateral (RB4) and medial (RB5). The right lower lobe bronchus has five segments: superior (RB6), medial basal (RB7), anterior basal (RB8), lateral basal (RB9), and posterior basal (RB10).

The left mainstem bronchus divides into the left upper and lower lobe bronchi. The left upper lobe bronchus subsequently divides into the left upper division bronchus and the lingular division. The former gives rise to three segments: apical (LB1), posterior (LB2), and anterior (LB3). The apical and posterior segments are usually fused in a single apicoposterior (LB1/2) segment. The lingular bronchus has two segments: superior lingular (LB4) and inferior lingular (LB5). The left lower lobe bronchus branches into the superior (LB6), anteromedial basal (LB7/8), lateral basal (LB9), and posterior basal (LB10) segments.

The bronchi undergo multiple divisions (on average 23) along the bronchial tree. The initial 16-17 generations of bronchi make up the conducting zone of the airways and do not participate in gas exchange. The surface of the airways that does not contribute to gas exchange is referred to as "dead space."

As these bronchi divide into smaller airways, the respiratory epithelium undergoes histological changes and gives rise to terminal bronchioles. The epithelium transitions from ciliated pseudostratified columnar to cuboidal epithelium. Goblet cells decrease in number, while club cells become prominent, producing surfactant-like substances to maintain airway patency. [8]

The 17th-19th generations of bronchioles constitute the transitional zone. These bronchioles enter pyramid-shaped pulmonary lobules separated from one another by a thin septum, with the apex directed toward the hilum, comprising 5-7 terminal bronchioles. The last 2-3 generations of bronchioles have some alveoli in their walls and make up the respiratory zone.

The area of the lung that is distal to a terminal bronchiole is termed the acinus. [9, 10]  The final division is called the respiratory bronchiole, which further branches into multiple alveolar ducts. Alveoli, the functional units of the respiratory system, start appearing at the level of the respiratory bronchioles.

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Microscopic Anatomy

The bronchial wall is made up of the following parts:

Mucosa: The mucosa is lined by a pseudostratified ciliated columnar epithelium. This epithelium is composed by ciliated columnar cells, goblet cells that produce mucus in order to trap irritants and expel them from the lungs, and basal cells which provide structural integrity and support regeneration and repair of the epithelium.

Lamina propria: A thin layer of connective tissue beneath the epithelium binding it to the smooth muscle.

Smooth muscle: It regulates the airway luminal diameter and modulates airway resistance.

Submucosa: The bronchial submucosa contains mixed compound tubuloacinar glands, which are mixed sero-mucous glands. These cells produce watery secretions that humidify inspired air in the bronchial lumen.

Interspersed cartilage: In the primary bronchi, the cartilage is in the form of C-shaped rings; as the bronchi branch, it becomes discontinuous and is replaced by smaller plates in distal sections.

The initial generations of the bronchi are similar to each other in their histological structure, except for the amount of hyaline cartilage. In the trachea, the cartilage encircles the lumen, but in the subsequent divisions of the bronchi, it is replaced by diminishing quantities of cartilage plates.

The bronchial mucosa is made of pseudostratified ciliated columnar epithelium with goblet cells and basal cells. Goblet cells are devoid of apical cilia and are responsible for mucous secretion. The density of goblet cells progressively decreases from the periphery and disappears at the level of terminal bronchioles. Basal cells are located close to the lamina propria. [10]  These progenitor basal cells support epithelial regeneration and repair. [4]

Mucin is a complex glycoprotein produced by goblet cells that is responsible for trapping particulate material (i.e., cells and debris) in the bronchi. The presence of mucin, water, and electrolytes ensures solubility of bronchial secretions.

Club (Clara) cells, located in the smaller bronchioles, secrete surfactant-like and antimicrobial proteins which regulate the inflammation and detoxification of the lungs.

Cilia present on the surface of epithelial cells provide rhythmic upward movement of bronchial secretions from within the lung to the pharynx. The respiratory epithelial cells are composed of basal bodies, also called terminal bars, which form a dark band just beneath the cilia and are modified centrioles.

The airway epithelial cells have apical junctions between them, comprising [11]

  • The zonula occludens (tight junctions) - Prevent paracellular leakage
  • The zonula adherens - Maintain structural integrity
  • The macula adherens (desmosomes) - Provide additional mechanical stability

Terminal bronchioles mark the transition from conducting airways to respiratory airways. [4]  The terminal bronchioles contain ciliated cuboidal epithelium, thin discontinuous smooth muscle, and submucosal connective tissue. Goblet cells are absent in the terminal bronchioles, while club cells are predominant. [12]

Respiratory bronchioles are partially lined by cuboidal epithelium; the remainder of their wall is lined by squamous epithelium. In contrast, alveolar walls are only composed of thin and flat squamous respiratory epithelium allowing for efficient gas exchange . [1]

Alveolar walls have thin squamous epithelium composed of: [13]

Type I pneumocytes: less numerous than type two and have more surface area as they specialize in gas exchange

Type II pneumocytes: more numerous than type one and are responsible for surfactant production to reduce surface tension

These walls also contain elastic fibers, capillary endothelium, and alveolar macrophages that collectively support efficient gas exchange and immune defense. [13]

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Natural and Pathophysiologic Variants

Minor anatomical tracheobronchial variations may be found incidentally during bronchoscopy and/or computed tomography scanning in 1-12% of patients. [14]  However, these are rarely clinically relevant and usually remain asymptomatic. Variations may include different branching patterns and accessory lobar or segmental bronchi.

Many airway diseases involve the bronchial tree in addition to lung parenchyma.

Asthma is a heterogeneous disease characterized by chronic inflammation and narrowing (bronchoconstriction) of the airways. It presents with respiratory symptoms such as wheezing, shortness of breath, chest tightness, and cough. Disease severity varies. [15]  It has a complex pathophysiology consisting of airway hyper-responsiveness, eosinophilic inflammation, and ultimately airway remodeling that leads to chronic obstruction. The mainstays of therapy are inhaled corticosteroids and bronchodilators. [16]  Systemic steroids may be used for severe exacerbations.

Cystic fibrosis is an autosomal recessive disease caused by a mutation in the cystic fibrosis transmembrane conductance regulator gene on chromosome 7. This mutation leads to abnormal development or function of the sodium channel in the luminal aspect of epithelial cells affecting the solubility of secretions, thus creating thick secretions. Particularly in the lungs, it causes decreased mucociliary clearance and subsequently recurrent lung infections. The disease may also affect other organs. [17]

Emphysema refers to permanent dilatation of the distal airways and alveolar wall damage. Parenchymal architectural destruction leads to airway obstruction through the loss of the elastic properties of the lung. Alveolar damage and replacement with large air sacs (bullae) leads to an impaired capacity for gas exchange.

Chronic bronchiectasis is characterized by persistent abnormal dilatation and destruction of the bronchi and bronchioles. This results in impaired drainage of secretions, airway obstruction, and subsequent recurrent lower respiratory tract infections. Clinically, it is characterized by chronic cough with sputum production and frequent acute exacerbations. [18]

Variants such as tracheal bronchus, accessory cardiac bronchus, and bridging bronchus are typically incidental findings. Most variations are asymptomatic but may occasionally present with complications such as recurrent pneumonia, hemoptysis, or bronchiectasis. Rare conditions such as situs inversus and bronchial isomerism are often associated with congenital heart disease or other syndromes (e.g., polysplenia or VACTERL syndrome) and may alter the branching patterns of the bronchial tree. [19]

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Other Considerations

Bronchoscopy is the process of direct visualization of the tracheobronchial tree. It may be performed using either a rigid bronchoscope or a flexible one. Flexible bronchoscopy is a minimally invasive procedure that can be performed with minimal preparation and sedation in an outpatient setting (see the video below). Conscious sedation is given before the procedure.

Video of flexible bronchoscopy in 2-year-old child. Bronchoscope has dual channels: one channel contains fiberoptic fibers; other contains port for suctioning. Scope is passed through left nasal passage. As it is passed through nasopharynx, epiglottis and larynx come into view; as it goes through vocal fold, subglottis and trachea become visible. Scope is then passed down left mainstem bronchus to visualize left upper and lower lobe bronchi. Next, scope is pulled back and passed down right mainstem bronchus. Right upper, middle, and lower lobe bronchi are then visualized. Video courtesy of Ravindhra G Elluru, MD, PhD.

Bronchoscopy enables visualization of the bronchial tree up to the level of the segmental bronchi and allows clinicians to obtain tissue and fluid samples from more distal airways and the lung parenchyma by means of bronchoalveolar lavage, brushings, and transbronchial biopsies. Microbiological and histopathological analyses of these samples facilitate the accurate diagnosis of various pulmonary diseases. Techniques such as endobronchial ultrasound and optical coherence tomography have enhanced diagnostic capabilities by providing real-time imaging of bronchial structures. [20]

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