Figures
Abstract
In the airway network of a human lung, the airway diameter gradually decreases through multiple branching. The diameter reduction ratio of the conducting airways that transport gases without gas exchange is 0.79, but this reduction ratio changes to 0.94 in acinar airways beyond transitional bronchioles. While the reduction in the conducting airways was previously rationalized on the basis of Murray’s law, our understanding of the design principle behind the acinar airways has been far from clear. Here we elucidate that the change in gas transfer mode is responsible for the transition in the diameter reduction ratio. The oxygen transfer rate per unit surface area is maximized at the observed geometry of acinar airways, which suggests the minimum cost for the construction and maintenance of the acinar airways. The results revitalize and extend the framework of Murray’s law over an entire human lung.
Citation: Park K, Jung Y, Son T, Cho Y-J, Jeon NL, Kim W, et al. (2019) Optimal diameter reduction ratio of acinar airways in human lungs. PLoS ONE 14(1): e0204191. https://doi.org/10.1371/journal.pone.0204191
Editor: Josué Sznitman, Technion Israel Institute of Technology, ISRAEL
Received: August 30, 2018; Accepted: January 16, 2019; Published: January 31, 2019
Copyright: © 2019 Park et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper.
Funding: H.-Y. Kim was supported by the National Research Foundation of Korea (grant no. 2018052541) via SNU IAMD. W. Kim was supported by the Korea Health Industry Development Institute (grant no. HI14C0746). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Fluid transport systems in the form of branching networks have evolved in multicellular organisms to deliver bulk metabolic matter to matter exchange sites [1–7]. In a branching network, a mother branch is divided into numerous terminal daughters. The aggregate cross-sectional area of the vessels of a single generation generally increases with branch generations, and the flow velocity thus decreases. A low flow speed is advantageous for allowing more time for mass transfer at the terminal branches [1]. For instance, the diameter of vascular vessels in the human body decreases from ~1 cm at the aortae to ~10 μm at the capillaries, whereas the aggregate cross-sectional area increases from ~1 cm2 to ~103 cm2 [1, 8]. However, expanding the cross-sectional area of the daughter vessels can be costly because of the construction and maintenance of redundant channels. Murray's law explains how the costs of running the vascular system can be minimized by controlling the diameter reduction ratio [9, 10]. The same framework has been utilized for rationalizing the observed diameter reduction ratio in the xylem in plants, for which the constructing cost of conduits is the primary factor limiting the expansion of the cross-sectional area of the xylem vessels [11].
The airway system in a human lung exhibits a similar branching architecture. A single trachea bifurcates into ~223 terminal branches. In this bronchial network, the expansion of the aggregate cross-sectional area of the daughter channels is limited by the airway volume, in such a way that the air transport to the alveoli is maximized for a given amount of inhalation air [12, 13]. Nevertheless, this rationale explains the airway branching only in conducting airways where no gas exchange occurs, as shown in Fig 1.
(A) Schematic illustration of conducting airways (blue box) and acinar airways (red box). The hierarchical airway network consists of dichotomous trees with 23 generations. The transferred air diffuses to capillaries enclosed in the alveoli, most of which are attached to the late generations of the airways. The airway lengths of the 16th-23rd generations are 1.33, 1.12, 0.93, 0.83, 0.7, 0.7, 0.7, and 0.7 mm in the order [12], and an average diameter of alveoli is 200 μm [34]. (B) Reduction in normalized airway diameter along with airway generation. The diameter reduction ratio is 0.79 in the conducting airways, whereas it shifts to 0.94 in the acinar airways. Note that Murray’s law for diffusion in insects, k = 0.71, cannot explain the acinar airways reduction ratio (red dashed line). Data were taken from Finlay [8] and Weibel [14].
It has been supposed that the change in gas transfer mode from advection to diffusion is responsible for the transition in the reduction ratio of bronchial airways [10, 14, 15]. Explicit analytical or computational studies, often combined with fractal modeling, focused on the velocity field in airways [16], permeability in acinus [17], breathing irregularity [18], and asymmetric branching [19–22]. The principle of the cost minimization for diffusive mass transfer was developed, which successfully provided the rationale for the spiracle pore networks of insects [23, 24]. However, this model cannot be directly applied to acinar airways because the observed diameter reduction ratio of acinar airways (k = 0.94) is much larger than that of Murray's law for diffusion (k = 0.71).
Here we present a model for the hitherto unexplained diameter reduction ratio in the acinar airways, k = 0.94. With a simplified airway geometry that is amenable to mathematical analysis, our model captures an essential physical picture responsible for the observed diameter reduction ratio.
Results
We begin with an analysis of the oxygen transfer in human lung airways. During a 2 s period of inhalation, a negative pressure in the pleural cavity induces the expansion of alveoli, and the total volume increase reaches approximately 500 ml [25]. As a result of the increase in the cross-sectional area of the airways, the average speed of the air flow decreases from about 0.5 m/s in the trachea to 1 μm/s in the alveoli. The dominant oxygen transfer mechanism can be examined using the Peclet number, Pe = ul/D, the ratio of the advective to the diffusive mass transfer rates, where l is the length of a single airway branch (l ~ 1 mm), u is the speed of the air flow, and D is the oxygen diffusion coefficient in air (D ~ 0.2 cm2/s). Using the data of the cross-sectional area of airways for each generation [8, 14], one can find that Pe < 1 after transitional bronchioles, which suggests a shift in the dominant oxygen transfer mechanism from advection to diffusion [10, 15].
We develop a mathematical model of the oxygen transport in the acinar airways. Since the oxygen transfer through the channels via diffusion depends on their cross-sectional area, a trumpet model can be used [26]. We construct a geometric model of the acinar airways as a stepwise channel with a unit depth by arranging all the channels side by side in such a way as to retain an equivalent aggregate cross-sectional area for each generation, as shown in Fig 2. The stepwise channel is further simplified as a diverging duct enclosed by two curved boundaries. Assuming that the transition of diameter reduction ratio occurs near the 16th branch, we can express the cross-sectional area as A(x) = A16ex/a with a = l/ln(2k2), where x is the distance from the 16th branch, A16 is the total cross-sectional area of the acinar airways at the 16th generation, and k is the diameter reduction ratio.
The acinar airways consist of eight generations of airways and alveoli. The acinar airways can be assumed as a bundle of rectangular channels with the identical cross-sectional area in the same generation. The sidewalls of the rectangular channels do not affect the vertical diffusion, so it can be assumed to be a single trumpet channel that expands like an exponential function involving the reduction ratio k and single channel length l.
Alveoli mediate oxygen transfer from the airways to the capillaries. Alveoli begin to appear from the transitional bronchioles, but most alveoli are attached to distal airways. Fig 3 shows the cumulated alveolar surface area with respect to airway generation [14, 17]. Assuming that the airway length in each generation is 1 mm, we formulate the cumulated alveolar surface area as a continuous function Aa(x) using spline interpolation, and the local alveolar surface area per unit length is given by Aa′(x) = dAa/dx. One can calculate the local oxygen transfer rate through alveoli per length as , where β is the solubility of oxygen in water [17], Dw is the diffusivity of oxygen in air, φ(x) is the partial pressure of oxygen in the acinar airways, φc is the oxygen partial pressure in the blood capillary, and h is the thickness of the alveolar membrane.
The circles denote the data obtained from [12], and the line is a spline interpolant Aa(x).
We examine the oxygen conservation in an infinitesimal control volume, as shown in Fig 2. Because sidewalls of a single airway prevent diffusion to neighboring airways, we only consider longitudinal diffusion along the x-axis,
(1)
where t is the time after inhalation begins. Solving Eq (1) requires an initial condition and two boundary conditions. We assume that the oxygen partial pressure in the acinar airways is the same as that of the blood capillary when inhalation begins because an exhalation time of ~ 2 s is greater than the diffusion time scale L2/(4D) ~ 0.8 s, where L ~ 8 mm is the diffusion length from the 16th to 23rd airways. Thus, the initial condition is written as φ(x, 0) = φc. Once inhalation begins, fresh air is supplied from the conducting airways. Accordingly, we assume that the oxygen partial pressure at the inlet of the 16th airway branch remains the same as that in the fresh air during the inhalation. This leads us to write a boundary condition as φ(0,t) = φa, where φa is the oxygen partial pressure in the fresh air. The other boundary condition comes from the 23rd generation where oxygen transfer is allowed only through the alveolar membrane, so that
.
By numerically solving Eq (1), we obtain the profile of oxygen partial pressure in acinar airways during the inhalation (see Materials and methods). Fig 4A shows the dimensionless oxygen partial pressure as a function of
for k = 0.9, which approaches the steady state profile within ~0.1 s. Hence, we neglect the unsteady effects in estimating the oxygen transfer during the whole inhalation process. Fig 4B and 4C show the profiles of the partial pressure and normalized oxygen transfer rate
to the blood capillaries, respectively, for various diameter reduction ratios (k = 0.7, 0.9 and, 1.1). Here
is defined as
(2)
with
so that the total area below a curve
is equal to unity.
(A) Temporal change in the distribution of the oxygen partial pressure for k = 0.9. (B) Profiles of the oxygen partial pressure for various diameter reduction ratios (k = 0.7, 0.9, and 1.1). (C) The dependence of the oxygen transfer to the blood capillaries on the airway depth. Note that the area below the curves is equal to unity by the definition of .
Acinar airways comprise a thin layer of epithelial cells covering airways and alveoli. Therefore, building an additional airway demands costs for construction and maintenance of the epithelial cell layer, which are proportional to the total surface area of the acinar airways. This reminds us of the fact that the expansion of the cross-sectional area in plant xylem vessels is limited by the carbon investment for the construction of the vessels [6]. We thus suggest that the total surface area of the acinar airways is the primary limiting factor.
Fig 5A displays the total oxygen transfer rate through the entire alveoli divided by the surface area of the acinar airways and alveoli versus the diameter reduction ratio. We see that although the total oxygen transfer rate increases with the diameter reduction ratio k, the sharp increase of the surface area with k results in the maximum Q/A at k = 0.94 (see Fig 5B). We thus infer that a ratio of 0.94 is the optimal reduction ratio to minimize the cost of the acinar airways for oxygen transfer. This theoretical value is indeed consistent with the biological data shown in Fig 1B. On the basis of the model, it can be deduced that the transition of the diameter reduction ratios between the conducting (k = 0.79) and acinar (k = 0.94) airways saves approximately 10% of the epithelial cell layers compared with the case without this transition. Consequently, our model suggests that this transition occurs for reducing energy and materials consumption in the acinar airways.
(A) Oxygen transfer rate per surface area of acinar airways and alveoli versus diameter reduction ratio. The oxygen transfer rate per surface area peaks at a diameter reduction ratio of 0.94, for which the energy cost for transporting a given amount of oxygen is minimized, provided that the energy investment is proportional to the surface area of acinar airways. (B) The dependence of oxygen transfer rate and surface area of acinar airways on the diameter reduction ratio. The values are normalized by their maximum values, respectively.
Discussion
The oxygen transfer to blood in acinar airways depends on the permeability of the alveolar membrane βDw/h, so that membrane permeability can change the optimal diameter reduction ratio. One can infer that the higher the permeability of the membrane, the less the surface required for a given amount of oxygen transfer. Hence, the more permeable alveoli would reduce the transfer through distal airways, referred to as ‘screening effects’ [17, 27], and reduce the effectiveness of distal airways. In Fig 6, we present the dependence of the oxygen transfer rate per surface area on the diameter reduction ratio for various permeability of the alveolar membrane. Indeed, the optimal diameter reduction ratio decreases with the membrane permeability, resulting in a smaller area of the terminal airways for higher permeability.
(A) Oxygen transfer rate per surface area versus diameter reduction ratio for various permeability. (B) The optimal diameter reduction ratios for various permeability.
Originally developed for blood vessels, Murray’s law describes branching structure for minimizing energy cost for convective transport and metabolism of blood [9, 10]. This design principle of branching structure has been used as a framework to understand various natural network systems under the assumption that natural branching networks have evolved in such a way as to minimize the cost for transferring a given quantity of matter [6, 7]. Murray’s law for conducting airways of lung explains the minimization of energy consumption for oxygen transport for a given volume of air inhalation [8, 10, 17]. Murray’s law for plant xylem elucidates the minimization of the primary energetic cost caused by sap flow and vessel construction [11]. Interestingly, despite various forms of energetic costs, Murray’s law for these networks commonly consider convection transport energy and vessel volume. Murray’s law for diffusion on the other hand can be formulated mathematically by replacing the energy cost for convective transport with the energy cost for diffusive transport, leading to an optimal diameter reduction ratio of 0.71 [23, 24].
However, the biological data of acinar airways in human lungs cannot be explained by either of the aforementioned models. We here raise in this report the question of transition of diameter reduction effects on lung optimization. Specifically, we consider the amount of diffusive transport of oxygen per surface area of airways. This implies that the dominant cost for the construction and maintenance of acinar airways comes from epithelial cell layers of airways and alveoli, which should be measured by the surface area rather than the volume.
Although advection is typically cost effective on the organismal scale, diffusion is a rapid, reliable, and cheap way to transfer matter on the cell scale [1, 28]. In mammals relying on air breathing, the characteristic diameter of the terminal branches of the airways is on the order of 100 μm, regardless of the body size [14, 29, 30]. Thus, gas transport via diffusion would be more effective near the terminal branches. Accordingly, the transition of the oxygen transfer mode is also expected in the lung airways of other species, which may cause the transition of the diameter reduction ratios. Indeed, some anatomical data on the lung airways of other species, including rats, rabbits, and canines, show a transition in the diameter reduction ratio as in human lung airways [29, 30], suggesting an interesting aspect worth pursuing in the future. This optimal strategy of acinar airways can guide design and construction of artificial networks where one needs to maximize fluid transport to a given area [31–33].
Materials and methods
We explain the process to solve Eq (1), the oxygen diffusion equation in the dichotomous hierarchical branch networks, subject to the boundary conditions:
(3)
Using the following dimensionless variables
we find dimensionless forms of Eqs (1) and (3):
(4)
(5)
Eq (4) with the initial and boundary conditions was solved numerically with parameters given in Table 1. Spatial derivatives in Eq (4) was discretized on uniformly spaced spatial grids (N = 100) using the second-order central difference scheme to obtain a system of ordinary differential equations (ODE) corresponding to a type of initial value problem. The resulting system of ODE is solved by a multistep method.
References
- 1. Labarbera M. Principles of design of fluid transport systems in zoology. Science. 1990;249(4972): 992–1000. pmid:2396104
- 2. Sapoval B, Filoche M. Magic trees in mammalians respiration or when evolution selected clever physical systems. Fractals. 2013;21(3–4): 1350024.
- 3. Park K, Kim W, Kim H-Y. Optimal lamellar arrangement in fish gills. Proc Natl Acad Sci U S A. 2014;111(22): 8067–8070. pmid:24847065
- 4. Noblin X, Mahadevan L, Coomaraswamy IA, Weitz DA, Holbrook NM, Zwieniecki MA. Optimal vein density in artificial and real leaves. Proc Natl Acad Sci U S A. 2008;105(27): 9140–9144. pmid:18599446
- 5. Price CA, Wing S, Weitz JS. Scaling and structure of dicotyledonous leaf venation networks. Ecol Lett. 2012;15(2): 87–95. pmid:22093803
- 6.
Bejan A. Shape and Structure, from Engineering to Nature. Cambridge Univ. Press; 2000
- 7.
Bejan A., Lorente S. Design with Constructal Theory: Wiley; 2008.
- 8. Finlay WH, Lange CF, King M, Speert DP. Lung delivery of aerosolized dextran. Am J Respir Crit Care Med. 2000;161(1): 91–97. pmid:10619803
- 9. Murray CD. The physiological principle of minimum work: I. The vascular system and the cost of blood volume. Proc Natl Acad Sci U S A. 1926;12(3): 207–214. pmid:16576980
- 10. Sherman TF. On connecting large vessels to small. The meaning of Murray's law. J Gen Physiol. 1981;78(4): 431–453. pmid:7288393
- 11. McCulloh KA, Sperry JS, Adler FR. Water transport in plants obeys Murray's law. Nature. 2003;421(6926): 939–942. pmid:12607000
- 12. Weibel ER, Sapoval B, Filoche M. Design of peripheral airways for efficient gas exchange. Respir Physiol Neurobiol. 2005;148(1–2): 3–21. pmid:15921964
- 13. Mauroy B, Filoche M, Weibel ER, Sapoval B. An optimal bronchial tree may be dangerous. Nature. 2004;427(6975): 633–636. pmid:14961120
- 14.
Weibel ER. Morphometry of the Human Lung. Berlin: Springer; 1963.
- 15. Weibel ER, Gomez DM. Architecture of the human lung. Science. 1962;137(3530): 577–585. pmid:14005590
- 16. Grebenkov DS, Filoche M, Sapoval B, Felici M. Diffusion-Reaction in Branched Structures: Theory and Application to the Lung Acinus. Phys Rev Lett. 2005;94(5): 050602. pmid:15783623
- 17. Sapoval B, Filoche M, Weibel ER. Smaller is better-but not too small: a physical scale for the design of the mammalian pulmonary acinus. Proc Natl Acad Sci U S A. 2002;99(16): 10411–10416. pmid:12136124
- 18. Hou C, Gheorghiu S, Huxley V, Pfeifer P. Reverse engineering of oxygen transport in the lung: Adaptation to changing demands and resources through space-filling networks. PLoS Comput Biol. 2010;6(8): e1000902. pmid:20865052
- 19.
Hou C, Gheorghiu S, Coppens M– O, Huxley VH, Pfeifer P. Gas diffusion through the fractal landscape of the lung: How deep does oxygen enter the alveolar system? In: Losa G, Merlini D, Nonnenmacher TF, Weibel ER, editors. Fractals in Biology and Medicine. Basel: Birkhäuser Basel; 2005. pp. 17–30.
- 20. Mauroy B, Bokov P. The influence of variability on the optimal shape of an airway tree branching asymmetrically. Phys Biol. 2010;7(1): 016007.
- 21. Florens M, Sapoval B, Filoche M. Optimal branching asymmetry of hydrodynamic pulsatile tree, Phys Rev Lett. 2011;106(17): 178104. pmid:21635067
- 22. Florens M, Sapoval B, Filoche M. An anatomical and functional model of the human tracheobronchial tree. J Appl Physiol. 2011;110(3): 756–763. pmid:21183626
- 23. Krogh A, Studien über Tracheenrespiration. II. Über Gasdiffusion in den Tracheen. Pflugers Arch Gesamte Physiol Menschen Tiere. 1920;179(1): 95–112.
- 24. Hertz SK, Bradley TJ. Insects breathe discontinuously to avoid oxygen toxicity. Nature. 2005;433(7025): 516–519. pmid:15690040
- 25.
West JB. Respiratory Physiology: The Essentials: Lippincott Williams & Wilkins; 2012.
- 26. Yu CP. Exact analysis of aerosol deposition during steady breathing. Powder Technol. 1978;21(1): 55–62.
- 27. Felici M, Filoche M, Sapoval B. Diffusional in the human pulmonary acinus. J Appl Physiol. 2003;94(5): 2010–2016. pmid:12679351
- 28.
Schmidt-Nielsen K. Scaling: Why is Animal Size So Important? Cambridge University Press; 1984.
- 29. Rodriguez M, Bur S, Favre A, Weibel ER. Pulmonary acinus: geometry and morphometry of the peripheral airway system in rat and rabbit. Am J Anat. 1987;180(2): 143–155. pmid:3673919
- 30. Horsfield K, Kemp W, Phillips S. An asymmetrical model of the airways of the dog lung. J Appl Physiol. 1982;52(1): 21–26. pmid:7061267
- 31. Park SJ, Gazzola M, Park KS, Park S, Di Santo V, Blevins EL, et al. Phototactic guidance of a tissue-engineered soft-robotic ray. Science. 2016;353(6295): 158–162. pmid:27387948
- 32. Zheng X, Shen G, Wang C, Li Y, Dunphy D, Hasan T, et al. Bio-inspired Murray materials for mass transfer and activity. Nat. Commun. 2017;8: 14921. pmid:28382972
- 33. Fan R, Sun Y, Wan J, Leaf-inspired artificial microvascular networks (LIAMN) for three-dimensional cell culture. RSC Adv. 2015;5(110): 90596–90601.
- 34. Ochs M, Nyengaard JR, Jung A, Knudsen L, Voigt M, Wahlers T, et al. The number of alveoli in the human lung. Am J Respir Crit Care Med. 2004;169(1): 120–124. pmid:14512270