| Home | E-Submission | Sitemap | Contact Us |  
Korean J Intern Med > Volume 16(3); 2001 > Article
Han, Chung, Ahn, Choi, Lee, Lee, and Sun: Ultrastructural Changes of Hepatic Stellate Cells in the Space of Disse in Alcoholic Fatty Liver


Background :

Hepatic stellate cell (HSC) has been suggested to play a role in fibrogenesis in alcoholic liver disease. We evaluate the correlation with fibrogenesis and ultrastructure of hepatic stellate cells in alcoholic fatty liver.

Methods :

We studied 6 patients with alcoholic fatty liver and 5 non-alcoholic fatty liver. The numbers of fat droplets in hepatic stellate cell was determined by electron microscopy. We also studied the grading of deposition of collagen fibers in the space of Disse. We were to evaluate the structure of hepatic stellate cells in the space of Disse by light and electron microscopy.

Results :

Wider distribution of fat droplets in hepatic stellate cells in alcoholic fatty liver than in normal liver. The hypertrophied endoplasmic reticulum in hepatic stellate cells is a prominent findings in alcoholic fatty liver. We observed basement membrane-like materials in patients with alcoholic fatty liver with hepatic fibrosis.

Conclusion :

The results demonstrate that, in patients with alcoholic fatty liver by alcoholic liver injury, the hepatic stellate cells may play an important role in the fibrogenesis of perisinusoidal spaces in the liver.


Recently it was reported that changes in eating patterns and drinking habits resulted in alcoholic liver disease1). Alcoholic liver disease is divided into alcoholic fatty liver, alcoholic hepatitis and alcoholic liver cirrhosis. The most common form is alcoholic fatty liver in the long-term alcohol drinker. One of the prominent morphologic findings of alcoholic liver damage is fibrogenesis consisting of collagen fibers in normal and edematous liver parenchyma and in the space of Disse2). It is well known which cells are involved in collagenization of hepatic lobules, but collagen fibers are originated from different cells according to the site of hepatic lobules and stages of lesion4). The liver comprises at least five different classes of cells. They are hepatocytes, fat- storing (Ito), endothelial, Kupffer and pit cells6). The main cell in the space of Disse is fat-storing (Ito) cells which are involved in hepatic fibrogenesis11, 12). The purpose of this study was to assess the fibrogenesis in the space of Disse and the role of hepatic stellate cell in patients with normal liver and alcoholic fatty liver under light and electron microscope, and to reveal the ultrastructural changes of hepatic stellate cells in the space of Disse.


Study population

We studied blind liver biopsy specimens from 13 normal subjects, 6 patients with alcoholic fatty liver, 3 patients with diabetic fatty liver and 2 patients with non-specific fatty liver. Twenty men and four women were enrolled in this study. The ages of the study subjects ranged from 21 to 48 years (mean age: 33.4 years).

Electron microscopy

For electron microscopy, the biopsied livers were rapidly cut into small pieces which were transferred to the following fixatives (pH 7.4) at 4°C: a) 2% glutaraldehyde Sorensen’s phosphate buffer for 3 hours b) 1% OsO4 phosphate buffer for 2 hours, followed by washing with same buffer and further incubated for 24–48 hours in a refrigerator (4°C). Sections were dehydrated with absolute ethanol and embedded in Epon 812. Observations were made on 0.5-μm thick Epon sections from controls that were stained with toluidine blue. After ultra-thin (600 Å) sectioning by ultramicrotome, the sections were lightly counter-stained with uranyl acetate and lead citrate and were analyzed by JEOL-100.

Counting of fat droplets of the hepatic stellate cell

Hepatic stellate cells in the space of Disse were observed and photographed using more than 2 blocks in each case. The numbers of fat droplets in 15–20 hepatic stellate cells, which were found in electron microscopy or photograph, were counted in each case.

Grading of collagenization in the space of Disse

We observed and photographed 10–20 space of Disse in all specimens using more than 2 blocks. Grading of deposition of collagen fibers in the space of Disse was done by using the modified scoring system of Orrego3). The extent and intensity of collagen fibers were graded on a scale of 0–3+ on two separate occasions and average score was calculated. A 3+ grade implies that basement membrane-like materials were found in subendothelial areas. A 2+ grade implies that space of Disse was distended by collagen fiber bundles which were also found in interhepatocellular space. A 1+ grade implies that 2–3 collagen fiber bundles were found in the space of Disse, while 0 implies that collagen fibers were absent throughout the specimen (Figure 1).

Statistical methods

Results were expressed as mean±SEM values. Student t-test or Mann-Whitney U test was used to determine the degree of difference between groups. A p value of less than 0.05 was considered significant.


Biochemical analysis

Major laboratory data was summarized in table 1. The serum albumin levels in two cases of alcoholic fatty liver and non-alcoholic fatty liver groups were below 3.0 g/dl. AST and ALT levels in all of alcoholic fatty liver and 3 of 5 cases of non-alcoholic fatty liver were mildly elevated compared with the control group. The serum bilirubin levels and thymol turbidity tests were not significantly higher than the control group (Table 1).

Distribution of the fat droplets in hepatic stellate cells and grading of collagenization

In comparing the numbers of fat droplets in control group (7.2±2.5), there was a significantly wider range of numbers in patients with alcoholic fatty liver (13.6±7.8) (p<0.05) and non-alcoholic fatty liver (12.0±7.1) (Figure 2).
The grading of collagenization was significantly higher in patients with alcoholic (1+ to 3+, mean 2.2+) and non-alcoholic fatty liver (1+ to 2+, mean 1.4+) than that in control group (0 to 1+) (Table 2). But there was no correlation between fibrosis and steatosis.

Light microscopic observations

Severe fat droplets infiltration throughout the entire hepatic lobules could be seen in patients with alcoholic fatty liver (Figure 3).
Mallory body was not seen in any of the cases. Most of the nuclei of hepatocytes were deviated by huge fat droplets (Figure 4). Glycogen nuclei were frequently observed in the cytoplasm of patients with non-alcoholic fatty liver complicated by diabetes mellitus.

Electron microscopic observations

In normal liver, hepatic stellate cells were mainly located in the space of Disse and the perisinusoidal recess (Figure 5, 10, 11,). The nuclei of hepatic stellate cells were heterochromatic and indented by fat droplets. One or two centrioles were observed in near well-developed Golgi apparatus (Figure 5) in patients with alcoholic fatty liver. The dense bodies and microfilament bundles with focal densities, a number of glycogen granules and pinocytotic vesicles were observed in the cytoplasm of hepatic stellate cells. Microfilaments (collagen fiber grading, 2+) in the space of Disse were gathered in bundles parallel to the plasma membrane (Figure 7). Basement membrane-like materials (collagen fiber grading, 3+) beneath the endothelial cells could be seen in patients with alcoholic fatty liver (Figure 8, 9). Also, we observed that bundles of coarse collagen fibers seemed to be arising from fat-storing cell surface in normal liver (Figure 10). Collagen fibers’ deposit in the space of Disse and changes of rough endoplasmic reticulum in hepatic stellate cells were observed in patients with alcoholic fatty liver. The hepatic stellate cells showed short, narrowed cisternae of endoplasmic reticulum and coarse collagen fibers in normal liver (Figure 5, 6). In patients with alcoholic fatty liver, hepatic stellate cells contained a number of endoplasmic reticulum whose cisternae were largely dilated (Figure 11) and filled with amorphous, fibrinoid materials (Figure 12). In patients with alcoholic fatty liver, the mitochondria were small in size and decreased in number. Also, sometimes, microtubules and lysosomes could be seen. Fat vacuoles, interestingly, showed variable sizes and were fused to each other in the liver of patients with alcoholic fatty liver (Figure 8, 13).


Alcohol causes a broad spectrum of liver disease, from fatty liver to cirrhosis. Alcoholic fatty liver is the most common and the least severe among those. One of the prominent histologic characteristics in alcoholic liver disease is interstitial fibrosis by collagen around swelled hepatocytes, which are frequently seen in centrilobular areas and result in bridging fibrosis from central areas to portal areas12). Mallory bodies are another important feature in alcoholic hepatitis, but these are frequently found in alcoholic cirrhrosis10). We could not observe the Mallory bodies in alcoholic fatty liver. The process of fibrosis continued without hepatitis or appearance of Mallory body in analcoholic baboon.
The electron microscopic observation of interstitial fibrosis of the liver is one of the prominent features of collagen deposition in the space of Disse that has profuse hepatic stellate cells and which is more common in alcoholic fatty liver than non-alcoholic one11). Many reports suggest that hepatic stellate cells of the liver (Ito cells or lipocytes) are responsible for this. However, the exact mechanism of collagen synthesis is still uncertain. Hepatic stellate cells of the liver are the principal collagen-producing cells in many liver diseases. Hepatic stellate cell activation and association with fibrosis, necroinflammatory activity, steatosis20). In alcoholic fatty liver, vitamin intoxication and long-term administration of alcohol, the number of hepatic stellate cells is decreased14). We studied to evaluate the correlation between alcohol and fibrosis by ultrastructural changes. We observed that the mean number of fat droplets per cell was significantly increased in patients with alcoholic fatty liver (1–60: mean 13.6) and non-alcoholic fatty liver (1–73: mean 12) than normal (1–33: mean 7.2). In previous studies, down-regulation of hepatic stellate cell may be associated with the appearance of transitional cells which have decreased number of fat droplets. In recent studies, the relationship between alcohol-induced hepatic stellate cells activation and severity of steatosis was shown14). We observed the same results that steatosis was closely related to the development of hepatic fibrosis. This is likely to reflect that both are attributable in part to the metabolic consequences of ethanol metabolism. We did not count hepatic stellate cells in each case. Also, we observed the microfilament bundles and dense bodies in hepatic stellate cells, suggesting transitional cells. Dense bodies may be the site of attaching the filament15). The existence of these organelles suggests that hepatic stellate cells are contractile cells. Contraction of these cells results in the contraction of sinusoids that are involved in the control of microcirculation in hepatic lobules16). The microcystic vesicles can be frequently observed in hepatic stellate cells, but their main function is not clear. Dilated cisternae of short and narrow endoplasmic reticulum in many hepatic stellate cells contain a flocculent material indicative of synthetic activity. In patients with alcoholic fatty liver with hepatic fibrosis, we observed basement membrane-like structure in the space of Disse beneath the endothelial cells. There is a direct correlation between the development of rough endoplasmic reticulum in hepatic stellate cells and the amount of collagen fibers5). We observed that the hypertrophy of rough endoplasmic reticulum in hepatic stellate cell is associated with the morphologic correlative of their activated fibrogenesis in the space of Disse. The microfilament and dense bodies are prominent features of myofibroblast concernied in fibrogenesis in alcoholic liver disease18). The myofibroblast exists in the area of the pericentral and sinusoid and is proliferated after alcohol administration. These cells produce type I, III and IV collagens19). The hepatic stellate cells, transitional cells and myofibroblasts are concerned in the fibrogenesis after liver injury20). It has been suggested that these cells have a common origin18, 21, 22). But the transformation of hepatic stellate cells to myofibroblasts should be further investigated. We observed a basement membrane-like structure in the space of Disse (so called “capillarization”) beneath the endothelial cells23). This capillarization of hepatic fibrogenesis interferes with the blood flow between sinusoid and hepatocytes, resulting in fibrogenesis and hepatic failure24). The preexisting sinusoid is changed functionally by newly developed collagen fibers4). The shunt formation between hepatic vein and portal vein, by overproduction of newly-developed vessels, is a compensatory mechanism for portal hypertension25). Hepatic stellate cell activation is a broad phenotypic response, characterized by distinct functional changes in proliferation, contractility, fibrogenesis26). Further insights into the regulation of hepatic stellate cells are believed to reduce morbidity and mortality in patients with chronic liver injury. The small number of patients was a limitation in this study for result analysis. Future studies, including many enrolled cases, will be needed for certifying our results.

Figure 1.
Gradings of collagen fibrils in space of Disse.
Figure 2.
Distribution of fat droplets in hepatic stellate cells of normal and fatty liver.
Figure 3.
Higher magnification of the fatty liver from a patient with alcoholic fatty liver. Large fat vacuoles were distending hepatocytes and several fat vacuoles have coalesced (H & E, ×400).
Figure 4.
Liver biopsy specimens from a patient with nonalcoholic fatty liver (case 11). Note severe fatty changes and increased portal fibrosis in the lower part (H & E, ×100).
Figure 5.
Electron micrograph of a hepatic stellate cell (HSC) in alcoholic fatty liver (case 5). HSC contained fat droplets (F) of variable sizes. HSC was separated from hepatocyte (H), endothelial cells and Kupffer cell (K) by space of Disse (DS) containing collagen fibrils and numerous microvilli. Ce; centriole (×10,000).
Figure 6.
Electron micrograph of hepatic stellate cell (HSC) from normal liver. HSC had well-developed Golgi apparatus and a few rough endoplasmic reticulum (arrows). H; hepatocyte, V; fat vacuole, F; fat droplet (×13,332).
Inset: higher magnification of a part of HSC showing well-developed Golgi apparatus (G), normally short, narrowed cisternae of endoplasmic reticulum (arrow) and glycogen granules in the cytoplasm. The Golgi apparatus consisted of several long and short, flattened cisternae and numerous vacuole (×26,664).
Figure 7.
Higher magnification of nuclear margin of hepatic stellate cell (HSC). At the periphery, microfilaments (arrow) were gathered in bundles parallel to the plasma membrane. Dense bodies (D) and pinocytotic vesicles (P) in close proximity to the cell surface were indicated. Bundles of coarse collagen fibers were present in the space of Disse (grade 2+) (×33,332).
Figure 8.
Electron micrograph of the liver of a patient with alcoholic fatty liver (case 4). Basement membrane-like material (arrows) existed (grade 3+) between the sinusoidal lining cell (E) and hepatocytes. Collagen fibers were also present in the intercellular space (grade 2+). A lymphocyte (L) had cytoplasmic projections in close proximity to the sinusoidal lining cell (E). Hepatocytes contained several fat vacuoles (V) (×10,000).
Figure 9.
Electron micrograph of the liver of a patient with alcoholic fatty liver (case 4) showing double layered basement membrane-like material (arrows) existing (grade 3+) beneath endothelial lining cell (E). The space of Disse (DS) containing fibers and microvilli was decreased. H; hepatocyte (×20,000).
Figure 10.
Electron micrograph of a hepatic stellate cell from normal liver. Coarse collagen fiber bundles (C) seemed to be arising from the cell surface. H; hepatocyte, F; fat vacuole (×10,000).
Figure 11.
Electron micrograph of the liver in a patient with alcoholic fatty liver. A hepatic stellate cell (HSC) was conspicuous with its abundant and well-developed rough endoplasmic reticulum (arrows). The space of Disse contained many collagen bundles (C) (grade 2+). The smooth endoplasmic reticulum of hepatocytes was hypertrophied. H; hepatocyte, F; fat vacuole (×10,000).
Figure 12.
Electron micrograph of a hepatic stellate cell (HSC) from normal liver. The HSC exhibited well-developed Golgi apparatus (G) and dilated endoplasmic reticulum (ER) which contained materials of the fluffy or fibrillar nature. Nc; nucleus (×20,000).
Figure 13.
Electron micrograph of the liver in a patient with alcoholic fatty liver (case 4). Hepatocytes contained fat vacuoles of variable sizes. Fat vacuoles showed invagination into small ones (×3,332).
Table 1.
Laboratory findings of patients with fatty liver
Cases Alcoholic fatty liver Non-alcoholic fatty liver
1 2 3 4 b 6 1 2 3 4 5
Age 32 41 44 31 37 23 39 42 26 41 61
Sex M M M M M M M M M M F

Total protein, g/dL 7.0 5.3 7.1 6.2 6.7 6.0 7.7 6.6 6.6 6.3 5.9
Albumin, g/dL 4.3 2.8 4.2 3.8 3.9 3.5 4.7 4.1 4.1 4.0 2.9
Globulin, g/dL 2.7 2.5 2.9 2.4 2.8 2.5 3.0 2.5 2.5 2.3 3.0
AST, IU/L 85 501 142 62 101 1,980 68 151 45 25 62
ALT, IU/L 66 132 83 120 25 650 114 185 67 35 34
Total cholesterol, mg/dL 127 137 307 186 200 167 167 - 184 128 151
Thymol turbidity, unit 3.2 1.6 6.5 3.4 1.1 9.3 1.9 9.4 2.1 1.5 12
Total bilirubin, mg/dL 1.0 1.0 1.2 0.9 6.7 25.2 0.9 0.9 0.5 1.1 0.5
Table 2.
Fat droplets of hepatic stellate cells and scores of collagen in the space of Disse in patients with fatty liver
Cases No. of fat droplets per hepatic stellate cell (HSC) Range Mean Collagen scores Steatosis
1 4–34 14.4 3+ 2+
2 8–28 12.8 3+ 1+
3 9–12 8.5 2+ 3+
4 1–13 7.2 2+ 2+
5 11–60 26.5 2+ 2+
6 3–17 7.0 1+ 1+
1 3–10 6.8 2+ 2+
2 1–73 26.1 2+ 1+
3 2–13 8.3 1+ 3+
4 3–21 9.6 1+ 2+
5 3–11 8.3 1+ 1+

AFL alcoholic fatty liver;

NAFL non-alcoholic fatty liver


1. Cha SB, Chung KW. Alcoholic liver disease in Korean. J Catholic Medical College 31:85–961978.

2. Hautekee ML, Geerts A, Seynaeve C, Lazou M, Kloppel G, Wisse E. Contributions of light and transmission electron microscopy to the study of the human fat-storing cell. Eur J Morphol 31:72–761993.
3. Orego H, Medline A, Blendis LM, Rankin JG, Kreaden A. Collagenization of the Disse space in alcoholic liver disease. Gut 20:673–6791979.
crossref pmid pmc
4. Popper H. Hepatic fibrosis. Correlation of biochemical and morphologic investigations. Am J Med 49:707–7211970.
crossref pmid
5. Minato Y, Hasumura Y, Takeuchi J. The role of fat-storing cells in Disse space fibrogenesis in alcoholic disease. Hepatology 3:559–5661983.
crossref pmid
6. Poulsen H, Christoffersen P. Connective tissue. Atlas of liver biopsies. 1st ed. Munksgaad, Copenhagen: J.B. Lippincott, 156. 1979.

7. Reppart JT, Peters RL, Edmondson HA, Baker RF. Electron and light microscopy sclerosing in hyaline necrosis of the liver. The development of alcoholic hyaline bodies. Lab invest 12:1138–11531963.
8. Flax MH, Tisdale WA. An electron microscopic study of alcoholic hyaline. Am J Path 44:441–4531964.
9. Popper H, Lieber CS. Histogenesis of alcoholic fibrosis and cirrhosis in the baboon. Am J Pathol 98:694–7151980.

10. Takada J. Pathogenesis and characteristics of alcoholic liver injury in Japan. J Jap Soc Intern Med 71:562–5671982.
11. Casini A, Galli G, Salzano R, Rotella CM, Surrenti C. Acetaldehyde-protein adducts, but not lactate and pyruvate, stimulate gene transcription of collagen and fibronectin in hepatic fat-storing cells. J Heptol 19:385–3921993.
12. Jones EA. Hepatic sinusoidal cells: new insights and controversies. Hepatology 3:259–2661983.
crossref pmid
13. Hruben Z, Russel RM, Boyer JL, Glagov S, Pagheri SA. Ultrastructural changes in liver of two patients with hypervitaminosis A. Am J Pathol 76:451–4681974.
pmid pmc
14. Reeves HL, Burt AD, Wood S, Day CP. Hepatic stellate cell activation occurs in the absence of hepatitis in alcoholic liver disease and correlates with the severity of steatosis. J Hepatol 25:677–6831996.
crossref pmid
15. Bond M, Somlyo AV. Dense bodies and actin polarity in vertebrate smooth muscle. J Cell Biol 95:403–4131982.
crossref pmid pmc
16. Wisse E. An electron microscopic study of the fenestrated endothelial lining of rat liver sinusoids. J Ultrastruct Res 31:125–1501970.
crossref pmid
17. Mann SW, Fuller GC, Rodil JV, Vidins E. Hepatic prolyl hydroxylase and collagen synthesis in patients with alcoholic liver disease. Gut 20:825–8321979.
crossref pmid pmc
18. Nakano M, Liever CS. Ultrastructure of initial stages of perivenular fibrosis in alcohol-fed baboons. Am J Pathol 106:145–1551982.
pmid pmc
19. Falchuk KR, Fiske SC, Haggitt RC, Federman M, Trey C. Pericentral hepatic fibrosis and intracellular hyalin in diabetes mellitus. Gastroenterology 78:535–5411980.
crossref pmid
20. Washington K, Wright K, Shyr Y, hunter EB, Olson S, Raiford DS. Hepatic stellate cell activation in nonalcoholic steatohepatitis and fatty liver. Hum pathol 31:822–8282000.
crossref pmid
21. Hay ED, Hasty DL, Keihanau KL. Morphological investigation of fibers derived from various types: fine structure of collagens and their relation to glycosaminoglycans (GAG), Collagen Platelet Interaction. In: Gastpar H, Kuhn K, Marx R, eds. Stuttgart-New York: F.K Schattauer Verlag, 129–1621978.

22. James WD, Odom RB. The role of the myofibroblast in Dupuytren’s contracture. Arch Dermatol 116:807–8111980.
crossref pmid
23. Schaffner PJ. Capillarization of hepatic sinusoids in man. Gastroenterology 44:239. 1963.
crossref pmid
24. Bhunchet E, Fujieda K. Capillarization and venulization of hepatic sinusoids in porcine serum-induced rat liver fibrosis: a mechanism to maintain liver blood flow. Hepatology 18:1450–14581993.
crossref pmid
25. Orrego H, Blendis LM, Crossiey IR, Macdonal A, Medline A, Ritchie S, Israel Y. Correction of intrahepatic pressure with collagen in the Disse space and hepatomegaly in humans and the rat. Gastroenterology 80:546–5561981.
crossref pmid
26. Friedman SL. Molecular mechanisms of hepatic fibrosis and principles of therapy. J Gastroenterology 32:424–4301997.
PDF Links  PDF Links
PubReader  PubReader
ePub Link  ePub Link
Full text via DOI  Full text via DOI
Full text via PMC  Full text via PMC
Download Citation  Download Citation
CrossRef TDM  CrossRef TDM
Related article
Editorial Office
101-2501, Lotte Castle President, 109 Mapo-daero, Mapo-gu, Seoul 04146, Korea
Tel: +82-2-2271-6792   Fax: +82-2-790-0993    E-mail: kaim@kams.or.kr
Copyright © 2020 The Korean Association of Internal Medicine. All rights reserved.
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
powerd by m2community