Expression of small heat shock protein αB-crystallin is induced after hepatic stellate cell activation

Author:

Lang Alon1,Schrum Laura W.2,Schoonhoven Robert3,Tuvia Shmuel4,Solís-Herruzo Jose A.1,Tsukamoto Hidekazu5,Brenner David A.16,Rippe Richard A.1

Affiliation:

1. Departments of Medicine,

2. Surgery,

3. Environmental Science and Engineering, and

4. Department of Cell Biology, Duke University, Durham, North Carolina 27710; and

5. Departments of Medicine and Pathology, University of Southern California, Los Angeles, California 90033

6. Biochemistry and Biophysics, University of North Carolina, Chapel Hill 27599; and

Abstract

Using the differential PCR display method to select cDNA fragments that are differentially expressed after hepatic stellate cell (HSC) activation, we have isolated from activated HSCs a cDNA that corresponds to rat αB-crystallin. Northern blots confirmed expression of αB-crystallin in culture-activated HSCs but not in quiescent HSCs. Western blot analysis and immunocytochemical staining confirmed expression of αB-crystallin protein in activated but not quiescent HSCs. αB-crystallin is induced as early as 6 h after plating HSCs on plastic and continues to be expressed for 14 days in culture. Expression of αB-crystallin was also induced in vivo in activated HSCs from experimental cholestatic liver fibrosis. Confocal microscopy demonstrated a cytoplasmic distribution of αB-crystallin in a cytoskeletal pattern. Heat shock treatment resulted in an immediate perinuclear redistribution that in time returned to a normal cytoskeletal distribution. The expression pattern of αB-crystallin was similar to that of HSP25, another small heat shock protein, but differed from the classic heat shock protein HSP70. Therefore, αB-crystallin represents an early marker for HSC activation.

Publisher

American Physiological Society

Subject

Physiology (medical),Gastroenterology,Hepatology,Physiology

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