The fractal geometry of bronchial trees differs by strain in mice

被引:7
作者
Glenny, Robb W. [1 ,2 ]
Krueger, Melissa [1 ]
Bauer, Christian [3 ]
Beichel, Reinhard R. [3 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Physiol & Biophys, Seattle, WA 98195 USA
[3] Univ Iowa, Dept Elect & Comp Engn, Iowa City, IA 52242 USA
关键词
airway; fractal; mouse; INBRED MOUSE STRAINS; VASCULAR TREE; DIMENSION; RESPONSIVENESS; MODEL;
D O I
10.1152/japplphysiol.00838.2019
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Fractal biological structures are pervasive throughout the plant and animal kingdoms, with the mammalian lung being a quintessential example. The lung airway and vascular trees are generated during embryogenesis from a small set of building codes similar to Turing mechanisms that create robust trees ideally suited to their functions. Whereas the blood flow pattern generated by these fractal trees has been shown to be genetically determined, the geometry of the trees has not. We explored a newly established repository providing high-resolution bronchial trees from the four most commonly studied laboratory mice (B6C3F1, BALB/c, C57BL/6 and CD-1). The data fit a fractal model well for all animals with the fractal dimensions ranging from 1.54 to 1.67, indicating that the conducting airway of mice can be considered a self-similar and space-filling structure. We determined that the fractal dimensions of these airway trees differed by strain but not sex, reinforcing the concept that airway branching patterns are encoded within the DNA. The observations also highlight that future study design and interpretations may need to consider differences in airway geometry between mouse strains. NEW & NOTEWORTHY Similar to larger mammals such as humans, the geometries of the bronchial tree in mice are fractal structures that have repeating patterns from the trachea to the terminal branches. The airway geometries of the four most commonly studied mice are different and need to be considered when comparing results that employ different mouse strains. This variability in mouse airway geometries should be incorporated into computer models exploring toxicology and aerosol deposition in mouse models.
引用
收藏
页码:362 / 367
页数:6
相关论文
共 41 条
  • [1] Fractal nature of regional ventilation distribution
    Altemeier, WA
    McKinney, S
    Glenny, RW
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 2000, 88 (05) : 1551 - 1557
  • [2] lapdMouse: associating lung anatomy with local particle deposition in mice
    Bauer, Christian
    Krueger, Melissa
    Lamm, Wayne J. E.
    Glenny, Robb W.
    Beichel, Reinhard R.
    [J]. JOURNAL OF APPLIED PHYSIOLOGY, 2020, 128 (02) : 309 - 323
  • [3] Beichel RR, 2019, LUNG ANATOMY PARTICL, DOI [10.25820/9arg-9w56, DOI 10.25820/9ARG-9W56]
  • [4] EFFICIENT BOX-COUNTING DETERMINATION OF GENERALIZED FRACTAL DIMENSIONS
    BLOCK, A
    VONBLOH, W
    SCHELLNHUBER, HJ
    [J]. PHYSICAL REVIEW A, 1990, 42 (04): : 1869 - 1874
  • [5] Bodduluri S, 2018, J CLIN INVEST, V128, P5374, DOI 10.1172/JCI120693
  • [6] Box-Counting Dimension Revisited: Presenting an Efficient Method of Minimizing Quantization Error and an Assessment of the Self-Similarity of Structural Root Systems
    Bouda, Martin
    Caplan, Joshua S.
    Saiers, James E.
    [J]. FRONTIERS IN PLANT SCIENCE, 2016, 7
  • [7] Lung hyperpermeability, CLARA-CELL secretory protein (CC16), and susceptibility to ozone of five inbred strains of mice
    Broeckaert, F
    Clippe, A
    Wattiez, R
    Falmagne, P
    Bernard, A
    [J]. INHALATION TOXICOLOGY, 2003, 15 (12) : 1209 - 1230
  • [8] Fractal dimension applied to plant identification
    Bruno, Odemir Martinez
    Plotze, Rodrigo de Oliveira
    Falvo, Mauricio
    de Castro, Mario
    [J]. INFORMATION SCIENCES, 2008, 178 (12) : 2722 - 2733
  • [9] Canals M, 2000, BIOL RES, V33, P31
  • [10] Bronchial responsiveness among inbred mouse strains - Role of airway smooth-muscle shortening velocity
    Duguet, A
    Biyah, K
    Minshall, E
    Gomes, R
    Wang, CG
    Taoudi-Benchekroun, M
    Bates, JHT
    Eidelman, DH
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (03) : 839 - 848