Liver fibrosis in elderly cadavers: Localization of collagen types I, III, and IV, α‐smooth muscle actin, and elastic fibers

KM Mak, E Chu, KHV Lau… - The Anatomical Record …, 2012 - Wiley Online Library
KM Mak, E Chu, KHV Lau, AJ Kwong
The Anatomical Record: Advances in Integrative Anatomy and …, 2012Wiley Online Library
We have shown a high prevalence of liver fibrosis in elderly cadavers with diverse causes of
death by Sirius red stain; however, the various collagen types in these samples have yet to
be evaluated. To further characterize the histopathology of the fibrotic lesions in the livers of
these elderly cadavers, this study used immunohistochemistry and histochemistry to identify
the principal collagens produced in liver fibrosis, fibrogenic cells and elastic fibers. Collagen
I and III immunoreactions were found to colocalize in collagen fibers of fibrotic central veins …
Abstract
We have shown a high prevalence of liver fibrosis in elderly cadavers with diverse causes of death by Sirius red stain; however, the various collagen types in these samples have yet to be evaluated. To further characterize the histopathology of the fibrotic lesions in the livers of these elderly cadavers, this study used immunohistochemistry and histochemistry to identify the principal collagens produced in liver fibrosis, fibrogenic cells and elastic fibers. Collagen I and III immunoreactions were found to colocalize in collagen fibers of fibrotic central veins, perisinusoidal fibrotic foci, portal tract stroma, and fibrous septa. α‐Smooth muscle actin‐expressing perisinusoidal hepatic stellate cells (HSCs), as well as perivenular, portal, and septal myofibroblasts, were closely associated with collagen fibers, reflecting their fibrogenic functions. HSCs and myofibroblasts were also noted to express collagen IV, which may contribute to production of basal lamina‐like structures. In fibrotic livers, the sinusoidal lining showed variable immunostaining for collagen IV. Collagen IV immunostaining revealed vascular proliferation and atypical ductular reaction at the portal–septal parenchymal borders, as well as capillary‐like vessels in the lobular parenchyma. While elastic fibers were absent in the space of Disse, they were found to codistribute with collagens in portal tracts, fibrous septa and central veins. Our combined assessment of collagen types, HSCs, myofibroblasts, and elastic fibers is significant in understanding the histopathology of fibrosis in the aging liver. Anat Rec, 2012. © 2012 Wiley Periodicals, Inc.
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