Literature DB >> 15385148

Systematic analysis of hematopoietic, vasculogenetic, and angiogenetic phases in the developing embryonic avian lung, Gallus gallus variant domesticus.

J N Maina1.   

Abstract

In the embryonic lung of the domestic fowl, Gallus gallus variant domesticus, hematogenetic and vasculogenetic cells become ultrastructurally clear from day 4 of development. In the former group of cells, filopodial extensions coalesce, cytoplasm thickens, and accumulating hemoglobin displaces the nucleus peripherally while in the latter, conspicuous filopodial extensions and large nuclei develop as the cells assume a rather stellate appearance. From day 5, erythrocytes and granular leukocytes begin forming from cytoarchitecturally cognate hematogenetic cells. The cells become distinguishable when hemoglobin starts to accumulate in the erythroblasts and electron dense bodies form in the leukoblasts. Vasculogenesis begins from day 7 in different areas of the developing lung: erthrocytes (but not granular leukocytes) appear to attract committed vasculogenetic cells (angioblasts) that form an endothelial lining and vessel wall. Arrangement of angioblasts around forming blood vessels sets the direction along which the vessels sprout (angiogenesis). In some areas of the developing lung, through what seems like an inductive erythropoietic process, arcades of erythrocytes organize. Once endothelial cells surround such continuities, discrete vascular units organize. By day 10, the major parts of the in-built (intrinsic) pulmonary vasculature are assembled. Complete pulmonary circulation (i.e., through the exchange tissue) is not established until after day 18 when the blood capillaries start to develop. Since the precursory erythrocytes do not have a respiratory role, it is imperative that de novo erythropoiesis is essential for vasculogenesis. Diffuse (fragmentary) development and subsequent piecemeal assembly of the pulmonary vascular system may explicate the fabrication of a complex circulatory architecture that grants cross-current, counter-current, and multicapillary serial arterialization designs in the exchange tissue of the avian lung. The exceptional respiratory efficiency of the avian lung is largely attributable to the geometries (physical interfacing) between the bronchial and vascular elements at different levels of morphological organization.

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Year:  2004        PMID: 15385148     DOI: 10.1016/j.tice.2004.05.002

Source DB:  PubMed          Journal:  Tissue Cell        ISSN: 0040-8166            Impact factor:   2.466


  5 in total

1.  Maturation of the fetal human choriocapillaris.

Authors:  Takayuki Baba; Rhonda Grebe; Takuya Hasegawa; Imran Bhutto; Carol Merges; D Scott McLeod; Gerard A Lutty
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-03-05       Impact factor: 4.799

Review 2.  Development of the human choriocapillaris.

Authors:  G A Lutty; T Hasegawa; T Baba; R Grebe; I Bhutto; D S McLeod
Journal:  Eye (Lond)       Date:  2010-01-15       Impact factor: 3.775

3.  The distribution and ultrastructure of the forming blood capillaries and the effect of apoptosis on vascularization in mouse embryonic molar mesenchyme.

Authors:  Guohua Yuan; Li Zhang; Guobin Yang; Jingwen Yang; Chunyan Wan; Lu Zhang; Guangtai Song; Shuo Chen; Zhi Chen
Journal:  Cell Tissue Res       Date:  2014-01-30       Impact factor: 5.249

Review 4.  Evolution of air breathing: oxygen homeostasis and the transitions from water to land and sky.

Authors:  Connie C W Hsia; Anke Schmitz; Markus Lambertz; Steven F Perry; John N Maina
Journal:  Compr Physiol       Date:  2013-04       Impact factor: 9.090

5.  Comparative molecular developmental aspects of the mammalian- and the avian lungs, and the insectan tracheal system by branching morphogenesis: recent advances and future directions.

Authors:  John N Maina
Journal:  Front Zool       Date:  2012-08-07       Impact factor: 3.172

  5 in total

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