4.6 Article

Growth of the airway smooth muscle layer from late gestation to childhood is mediated initially by hypertrophy and subsequently hyperplasia

Journal

RESPIROLOGY
Volume 27, Issue 7, Pages 493-500

Publisher

WILEY
DOI: 10.1111/resp.14240

Keywords

airway smooth muscle; asthma; extracellular matrix; hyperplasia; hypertrophy; ontogeny; remodelling

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico
  2. National Health and Medical Research Council [1045824, 1077791, 1090888, 1120128]
  3. Sir Charles Gairdner and Osborne Park Health Care Group Research Advisory Committee
  4. Medical and Health Research Infrastructure Fund
  5. Western Australian Department of Health -Merit Award
  6. National Health and Medical Research Council of Australia [1120128, 1077791] Funding Source: NHMRC

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This study investigates the thickening process of the airway smooth muscle (ASM) layer from fetal life to childhood, and reveals the underlying mechanisms of hypertrophy, hyperplasia, and extracellular matrix (ECM) deposition. The results show that ASM thickness more than doubles from late gestation to the first year of life due to ASM hypertrophy, and then grows proportionally to airway size through ASM hyperplasia until childhood. The composition of the ASM layer remains constant across age groups due to a proportional change in ECM.
Background and objective The airway smooth muscle (ASM) layer thickens during development. Identifying the mechanism(s) for normal structural maturation of the ASM reveals pathways susceptible to disease processes. This study characterized thickening of the ASM layer from foetal life to childhood and elucidated the underlying mechanism in terms of hypertrophy, hyperplasia and extracellular matrix (ECM) deposition. Methods Airways from post-mortem cases were examined from seven different age groups: 22-24 weeks gestation, 25-31 weeks gestation, term (37-41 weeks gestation), <0.5 year, 0.5-1 year, 2-5 years and 6-10 years. The ASM layer area (thickness), the number and size of ASM cells and the volume fraction of ECM were assessed by planimetry and stereology. Results From late gestation to the first year of life, normalized ASM thickness more than doubled as a result of ASM hypertrophy. Thereafter, until childhood, the ASM layer grew in proportion to airway size, which was mediated by ASM hyperplasia. Hypertrophy and hyperplasia of ASM were accompanied by a proportional change in ECM such that the broad composition of the ASM layer was constant across age groups. Conclusion These data suggest that the mechanisms of ASM growth from late gestation to childhood are temporally decoupled, with early hypertrophy and subsequent proliferation. We speculate that the developing airway is highly susceptible to ASM thickening in the first year of life and that the timing of an adverse event will determine structural phenotype.

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