Massive hepatic necrosis (MHN) is a condition that offers an opportunity to study
the remarkable ability of the liver to become repopulated with hepatocytes. A maximal
regenerative stimulus is expected in cases of MHN (Roskams et al. APMIS Suppl 1991;23:32-39).
Sequential chronological observations, after a severe degree of liver cell loss, permit
study of the human equivalent of the situation in animal models in which circulating
and bone marrow-derived stem and liver progenitor cells are recruited to the hepatopoietic
process. To date, the bone marrow and circulating precursors have not been identified
morphologically in human material. We present data that suggest that the circulating
liver progenitor could have a lymphoblastoid morphological appearance. Similar cells
are seen among the cellular infiltrate of MHN. We have found that combinations of
markers, such as CD117/CD133 positive CD45/tryptase negative are useful to isolate
these cells using cell-sorting technology. This may facilitate their expansion in
vitro and the development of their use for therapeutic purposes. In MHN, the residual
portal tracts and ductular reaction with the associated lymphoid infiltrate (some
of which are probably liver cell progenitors derived from the circulation) constitute
the fundamental regenerative community unit in which hepatopoiesis takes place. Defining
the hepatopoietic process is hindered by the lack of morphological transitional forms
in the period between the progenitors within the circulation and when they assume
recognizable hepatocytic form as “metaplastic” hepatocytes associated with the ductular
reaction. By achieving a better comprehension of these processes of liver cell restoration,
we will be better placed to accelerate liver recovery in MHN, for example by the administration
of granulocyte colony stimulating factor (GCSF). Thus, more patients will be able
to restore their own livers and avoid liver transplantation.
KEYWORDS
Stem cells - progenitor cells - regeneration - transdifferentiation - massive hepatic
necrosis - CD117 - CD133
REFERENCES
- 1
Reuben A.
The last gasp or caveat cenans!.
Hepatology.
2003;
38
273-276
- 2
Rakela J, Perkins J D, Gross Jr J B et al..
Acute hepatic failure: the emerging role of orthotopic liver transplantation.
Mayo Clin Proc.
1989;
64
424-428
- 3
Sheil A G, McCaughan G W, Isai H I et al..
Acute and subacute fulminant hepatic failure: the role of liver transplantation.
Med J Aust.
1991;
154
724-728
- 4
Chenard-Neu M P, Boudjema K, Bernuau J et al..
Auxiliary liver transplantation: regeneration of the native liver and outcome in 30
patients with fulminant hepatic failure-a multicenter European study.
Hepatology.
1996;
23
1119-1127
- 5
Hodgson H.
Liver cells: biology to therapeutics.
Clin Med.
2003;
3
161-165
- 6
Korbling M, Estrov Z.
Adult stem cells for tissue repair-a new therapeutic concept?.
N Engl J Med.
2003;
349
570-582
- 7
Hanau C, Munoz S J, Rubin R.
Histopathological heterogeneity in fulminant hepatic failure.
Hepatology.
1995;
21
345-351
- 8
Thung S N, Gerber M A.
The formation of elastic fibers in livers with massive hepatic necrosis.
Arch Pathol Lab Med.
1982;
106
468-469
- 9
Scheuer P J, Maggi G.
Hepatic fibrosis and collapse: histological distinction by orecin staining.
Histopathology.
1980;
4
487-490
- 10
Lesna M, Watson A J, Douglas A P et al..
Evaluation of paracetamol-induced damage in liver biopsies. Acute changes and follow-up
findings.
Virchows Arch A Pathol Anat Histol.
1976;
370
333-344
- 11
Portmann B, Talbot I C, Day D W et al..
Histopathological changes in the liver following a paracetamol overdose: correlation
with clinical and biochemical parameters.
J Pathol.
1975;
117
169-181
- 12 Davies S E, Portmann B C. Drugs and toxins. In: Wight DGD Liver, Biliary Tract
and Exocrine Pancreas. London; Churchill Livingstone 1994: 201-236
- 13
Sell S.
Heterogeneity and plasticity of hepatocyte lineage cells.
Hepatology.
2001;
33
738-750
- 14
Michalopoulos G K, DeFrances M C.
Liver regeneration.
Science.
1997;
276
60-66
- 15
Alison M R.
Regulation of hepatic growth.
Physiol Rev.
1986;
66
499-541
- 16
Rabes H M, Wirsching R, Tuczek H V, Iseler G.
Analysis of cell cycle compartments of hepatocytes after partial hepatecomy.
Cell Tissue Kinet.
1976;
9
517-532
- 17
Overturf K, Al Dhalimy M, Ou C N et al..
Serial transplantation reveals the stem-cell-like regenerative potential of adult
mouse hepatocytes.
Am J Pathol.
1997;
151
1273-1280
- 18
Saxena R, Theise N.
Canals of Hering: recent insights and current knowledge.
Semin Liver Dis.
2004;
1
43-48
- 19
Yin L, Lynch D, Ilic Z, Sell S.
Proliferation and differentiation of ductular progenitor cells and littoral cells
during the regeneration of the rat liver to CCl4/2-AAF injury.
Histol Histopathol.
2002;
17
65-81
- 20
Demetris A J, Seaberg E C, Wennerberg A et al..
Ductular reaction after submassive necrosis in humans. Special emphasis on analysis
of ductular hepatocytes.
Am J Pathol.
1996;
149
439-448
- 21
Roskams T, De Vos R, Van Eyken P et al..
Hepatic OV-6 expression in human liver disease and rat experiments: evidence for hepatic
progenitor cells in man.
J Hepatol.
1998;
29
455-463
- 22
Petersen B E, Bowen W C, Patrene K D et al..
Bone marrow as a potential source of hepatic oval cells.
Science.
1999;
284
1168-1170
- 23
Theise N D, Badve S, Saxena R et al..
Derivation of hepatocytes from bone marrow cells in mice after radiation-induced myeloablation.
Hepatology.
2000;
31
235-240
- 24
Alison M R, Poulsom R, Jeffery R et al..
Hepatocytes from non-hepatic adult stem cells.
Nature.
2000;
406
257
- 25
Theise N D, Nimmakayalu M, Gardner R et al..
Liver from bone marrow in humans.
Hepatology.
2000;
32
11-16
- 26
Korbling M, Katz R L, Khanna A et al..
Hepatocytes and epithelial cells of donor origin in recipients of peripheral-blood
stem cells.
N Engl J Med.
2002;
346
738-746
- 27
Lagasse E, Connors H, Al Dhalimy M et al..
Purified hematopoietic stem cells can differentiate into hepatocytes in vivo.
Nat Med.
2000;
6
1229-1234
- 28
Krause D S, Theise N D, Collector M I et al..
Multi-organ, multi-lineage engraftment by a single bone marrow-derived stem cell.
Cell.
2001;
105
369-377
- 29
Wurmser A E, Gage F H.
Stem cells: cell fusion causes confusion.
Nature.
2002;
416
485-487
- 30
Terada N, Hamazaki T, Oka M et al..
Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion.
Nature.
2002;
416
542-545
- 31
Ying Q L, Nichols J, Evans E P, Smith A G.
Changing potency by spontaneous fusion.
Nature.
2002;
416
545-548
- 32
Wang X, Willenbring H, Akkari Y et al..
Cell fusion is the principal source of bone-marrow-derived hepatocytes.
Nature.
2003;
422
897-901
- 33
Vassilopoulos G, Wang P R, Russell D W.
Transplanted bone marrow regenerates liver by cell fusion.
Nature.
2003;
422
901-904
- 34
Forbes S J, Vig P, Pearce D et al..
Bone marrow-hepatocytes transdifferentiation: this axis of organ regeneration can
be modulated for clnical application.
J Hepatol.
2003;
38(suppl 2)
32
- 35
Newsome P N, Johannessen I, Boyle S et al..
Human cord blood-derived cells can differentiate into hepatocytes in the mouse liver
with no evidence of cellular fusion.
Gastroenterology.
2003;
124
1891-1900
- 36
Libbrecht L, Roskams T.
Hepatic progenitor cells in human liver diseases.
Semin Cell Dev Biol.
2002;
13
389-396
- 37
Koukoulis G, Rayner A, Tan K C et al..
Immunolocalization of regenerating cells after submassive liver necrosis using PCNA
staining.
J Pathol.
1992;
166
359-368
- 38
Braun K M, Sandgren E P.
Cellular origin of regenerating parenchyma in a mouse model of severe hepatic injury.
Am J Pathol.
2000;
157
561-569
- 39
Bralet M P, Branchereau S, Brechot C, Ferry N.
Cell lineage study in the liver using retroviral mediated gene transfer. Evidence
against the streaming of hepatocytes in normal liver.
Am J Pathol.
1994;
144
896-905
- 40
Ponder K P.
Analysis of liver development, regeneration, and carcinogenesis by genetic marking
studies.
FASEB J.
1996;
10
673-682
- 41
Kennedy S, Rettinger S, Flye M W, Ponder K P.
Experiments in transgenic mice show that hepatocytes are the source for postnatal
liver growth and do not stream.
Hepatology.
1995;
22
160-168
- 42
Zhao M, Laissue J A, Zimmermann A.
TUNEL-positive hepatocytes in alcoholic liver disease. A retrospective biopsy study
using DNA nick end-labelling.
Virchows Arch.
1997;
431
337-344
- 43
Ng I O, Burroughs A K, Rolles K et al..
Hepatocellular ballooning after liver transplantation: a light and electronmicroscopic
study with clinicopathological correlation.
Histopathology.
1991;
18
323-330
- 44
De Priester W, Van Manen R, Knook D L.
Lysosomal activity in the aging rat liver. II. Morphometry of acid phosphatase positive
dense bodies.
Mech Aging Dev.
1984;
26
205-216
- 45
Kishi M, Maeyama S, Koike J et al..
Correlation between intrasinusoidal neutrophilic infiltration and ceroid-lipofuscinosis
in alcoholic liver fibrosis with or without fatty change: clinicopathological comparison
with nutritional fatty liver.
Alcohol Clin Exp Res.
1996;
20 (Suppl 9)
366A-370A
- 46
Ishida M, Nakagawara G, Imamura Y, Fukuda M.
Iron and copper deposition in chronic active hepatitis and liver cirrhosis; pathogenetic
role in progressive liver cell damage.
Eur J Histochem.
1995;
39
221-236
- 47
Kitada T, Seki S, Iwai S et al..
In situ detection of oxidative DNA damage, 8-hydroxydeoxyguanosine, in chronic human
liver disease.
J Hepatol.
2001;
35
613-618
- 48
Seki S, Kitada T, Yamada T et al..
In situ detection of lipid peroxidation and oxidative DNA damage in non-alcoholic
fatty liver diseases.
J Hepatol.
2002;
37
56-62
- 49
Seki S, Kitada T, Sakaguchi H et al..
Pathological significance of oxidative cellular damage in human alcoholic liver disease.
Histopathology.
2003;
42
365-371
- 50
Tsurudome Y, Hirano T, Hirata K et al..
Age-associated increase of 8-hydroxydeoxyguanosine in human colorectal tissue DNA.
J Gerontol A Biol Sci Med Sci.
2001;
56
B483-B485
- 51
Sai K, Takagi A, Umemura T et al..
Changes of 8-hydroxydeoxyguanosine levels in rat organ DNA during the aging process.
J Environ Pathol Toxicol Oncol.
1992;
11
139-143
- 52
Allsop R C, Harley C B.
Evidence for a critical telomere length in senescent human fibroblasts.
Exp Cell Res.
1995;
219
130-136
- 53
Hayflick L.
Mortality and immortality at the cellular level. A review.
Biochemistry (Mosc).
1997;
62
1180-1190
- 54
Severino J, Allen R G, Balin S et al..
Is beta-galactosidase staining a marker of senescence in vitro and in vivo?.
Exp Cell Res.
2000;
257
162-171
- 55
Dimri G P, Lee X, Basile G et al..
A biomarker that identifies senescent human cells in culture and in aging skin in
vivo.
Proc Natl Acad Sci USA.
1995;
92
9363-9367
- 56
Paradis V, Youssef N, Dargere D et al..
Replicative senescence in normal liver, chronic hepatitis C, and hepatocellular carcinomas.
Hum Pathol.
2001;
32
327-332
- 57
Theise N D, Saxena R, Portmann B C et al..
The canals of Hering and hepatic stem cells in humans.
Hepatology.
1999;
30
1425-1433
- 58
Phillips M J, Poucell S.
Modern aspects of the morphology of viral hepatitis.
Hum Pathol.
1981;
12
1060-1084
- 59
Petersen B E, Grossbard B, Hatch H et al..
Mouse A6-positive hepatic oval cells also express several hematopoietic stem cell
markers.
Hepatology.
2003;
37
632-640
- 60
Omori N, Omori M, Evarts R P et al..
Partial cloning of rat CD34 cDNA and expression during stem cell-dependent liver regeneration
in the adult rat.
Hepatology.
1997;
26
720-727
- 61
Fujio K, Evarts R P, Hu Z et al..
Expression of stem cell factor and its receptor, c-kit, during liver regeneration
from putative stem cells in adult rat.
Lab Invest.
1994;
70
511-516
- 62
Omori M, Omori N, Evarts R P et al..
Coexpression of flt-3 ligand/flt-3 and SCF/c-kit signal transduction system in bile-duct-ligated
SI and W mice.
Am J Pathol.
1997;
150
1179-1187
- 63
Petersen B E, Goff J P, Greenberger J S, Michalopoulos G K.
Hepatic oval cells express the hematopoietic stem cell marker Thy-1 in the rat.
Hepatology.
1998;
27
433-445
- 64
Ma X, Qiu D K, Peng Y S.
Immunohistochemical study of hepatic oval cells in human chronic viral hepatitis.
World J Gastroenterol.
2001;
7
238-242
- 65
Seki S, Kitada T, Sakaguchi H et al..
Expression of progenitor cell markers in livers with fulminant massive necrosis.
Hepatol Res.
2003;
25
149-157
- 66
Ros J E, Libbrecht L, Geuken M et al..
High expression of MDR1, MRP1, and MRP3 in the hepatic progenitor cell compartment
and hepatocytes in severe human liver disease.
J Pathol.
2003;
200
553-560
- 67
Alison M R.
Tissue-based stem cells: ABC transporter proteins take centre stage.
J Pathol.
2003;
200
547-550
- 68
Lazaro C A, Rhim J A, Yamada Y, Fausto N.
Generation of hepatocytes from oval cell precursors in culture.
Cancer Res.
1998;
58
5514-5522
- 69
Wang J, Clark J B, Rhee G S et al..
Proliferation and hepatic differentiation of adult-derived progenitor cells.
Cells Tissues Organs.
2003;
173
193-203
- 70
Evarts R P, Nagy P, Nakatsukasa H et al..
In vivo differentiation of rat liver oval cells into hepatocytes.
Cancer Res.
1989;
49
1541-1547
- 71
Thorgeirsson S S, Evarts R P, Bisgaard H C et al..
Hepatic stem cell compartment: activation and lineage commitment.
Proc Soc Exp Biol Med.
1993;
204
253-260
- 72
Chen J Z, Hong H, Xiang J et al..
A selective tropism of transfused oval cells for liver.
World J Gastroenterol.
2003;
9
544-546
- 73
Cassell H S, Price P, Olver S D, Yeoh G C.
The association between murine cytomegalovirus induced hepatitis and the accumulation
of oval cells.
Int J Exp Pathol.
1998;
79
433-441
- 74
Ihrig M, Schrenzel M D, Fox J G.
Differential susceptibility to hepatic inflammation and proliferation in AXB recombinant
inbred mice chronically infected with Helicobacter hepaticus.
Am J Pathol.
1999;
155
571-582
- 75
Libbrecht L, Desmet V, Van Damme B, Roskams T.
Deep intralobular extension of human hepatic “progenitor cells” correlates with parenchymal
inflammation in chronic viral hepatitis: can “progenitor cells” migrate?.
J Pathol.
2000;
192
373-378
- 76
Sell S.
Electron microscopic identification of putative liver stem cells and intermediate
hepatocytes following periportal necrosis induced in rats by allyl alcohol.
Stem Cells.
1997;
15
378-385
- 77
Craig C EH, Quaglia A, Savage K et al..
Hepatocyte progenitor cells in massive hepatic necrosis.
J Hepatol.
2003;
38 (Suppl 2)
38
- 78
Dabeva M D, Shafritz D A.
Activation, proliferation, and differentiation of progenitor cells into hepatocytes
in the D-galactosamine model of liver regeneration.
Am J Pathol.
1993;
143
1606-1620
- 79
Dabeva M D, Laconi E, Oren R et al..
Liver regeneration and alpha-fetoprotein messenger RNA expression in the retrorsine
model for hepatocyte transplantation.
Cancer Res.
1998;
58
5825-5834
- 80
Dabeva M D, Petkov P M, Sandhu J et al..
Proliferation and differentiation of fetal liver epithelial progenitor cells after
transplantation into adult rat liver.
Am J Pathol.
2000;
156
2017-2031
- 81
Gerber M A, Thung S N, Shen S et al..
Phenotypic characterization of hepatic proliferation. Antigenic expression by proliferating
epithelial cells in fetal liver, massive hepatic necrosis, and nodular transformation
of the liver.
Am J Pathol.
1983;
110
70-74
- 82
Libbrecht L, Desmet V, Van Damme B, Roskams T.
The immunohistochemical phenotype of dysplastic foci in human liver: correlation with
putative progenitor cells.
J Hepatol.
2000;
33
76-84
- 83
Baumann U, Crosby H A, Ramani P et al..
Expression of the stem cell factor receptor c-kit in normal and diseased pediatric
liver: identification of a human hepatic progenitor cell?.
Hepatology.
1999;
30
112-117
- 84
Badve S, Logdberg L, Sokhi R et al..
An antigen reacting with das-1 monoclonal antibody is ontogenically regulated in diverse
organs including liver and indicates sharing of developmental mechanisms among cell
lineages.
Pathobiology.
2000;
68
76-86
- 85
Prost S, LeDiscorde M, Haddad R et al..
Characterization of a novel hematopoietic marker expressed from early embryonic hematopoietic
stem cells to adult mature lineages.
Blood Cells Mol Dis.
2002;
29
236-248
- 86
Blakolmer K, Jaskiewicz K, Dunsford H A, Robson S C.
Hematopoietic stem cell markers are expressed by ductal plate and bile duct cells
in developing human liver.
Hepatology.
1995;
21
1510-1516
- 87
Lemmer E R, Shepard E G, Blakolmer K et al..
Isolation from human fetal liver of cells co-expressing CD34 haematopoietic stem cell
and CAM 5.2 pancytokeratin markers.
J Hepatol.
1998;
29
450-454
- 88
Crosby H A, Kelly D A, Strain A J.
Human hepatic stem-like cells isolated using c-kit or CD34 can differentiate into
biliary epithelium.
Gastroenterology.
2001;
120
534-544
- 89
Zhao Y, Glesne D, Huberman E.
A human peripheral blood monocyte-derived subset acts as pluripotent stem cells.
Proc Natl Acad Sci USA.
2003;
100
2426-2431
- 90
Wang X, Ge S, McNamara G et al..
Albumin-expressing hepatocyte-like cells develop in the livers of immune-deficient
mice that received transplants of highly purified human hematopoietic stem cells.
Blood.
2003;
101
4201-4208
- 91
Oberlin E, Tavian M, Blazsek I, Peault B.
Blood-forming potential of vascular endothelium in the human embryo.
Development.
2002;
129
4147-4157
- 92
Hu Z J, Lang Z W, Song C Z, Zhang S J.
[Detection of hepatic progenitor cells in patients with severe hepatitis and their
distribution.]
Zhonghua Gan Zang Bing Za Zhi.
2003;
11
394-397
- 93
Goodell M A, Rosenzweig M, Kim H et al..
Dye efflux studies suggest that haematopoietic stem cells expressing low or undetectable
levels of CD34 antigen exist in multiple species.
Nat Med.
1997;
3
1337-1345
- 94
de Miguel M P, Cheng L, Holland E C et al..
Dissection of the c-Kit signaling pathway in mouse primordial germ cells by retroviral-mediated
gene transfer.
Proc Natl Acad Sci USA.
2002;
99
10458-10463
- 95
Broxmeyer H E, Maze R, Miyazawa K et al..
The kit receptor and its ligand, steel factor, as regulators of hemopoiesis.
Cancer Cells.
1991;
3
480-487
- 96
Armbrust T, Batusic D, Ringe B, Ramadori G.
Mast cells distribution in human liver disease and experimental rat liver fibrosis.
Indications for mast cell participation in development of liver fibrosis.
J Hepatol.
1997;
26
1042-1054
- 97
Simpson K, Hogaboam C M, Kunkel S L et al..
Stem cell factor attenuates liver damage in a murine model of acetaminophen-induced
hepatic injury.
Lab Invest.
2003;
83
199-206
- 98
Miraglia S, Godfrey W, Yin A H et al..
A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization,
and molecular cloning.
Blood.
1997;
90
5013-5021
- 99
Yin A H, Miraglia S, Zanjani E D et al..
AC133, a novel marker for human hematopoietic stem and progenitor cells.
Blood.
1997;
90
5002-5012
- 100
Gallacher L, Murdoch B, Wu D M et al..
Isolation and characterization of human CD34(-)Lin(-) and CD34(+)Lin(-) hematopoietic
stem cells using cell surface markers AC133 and CD7.
Blood.
2000;
95
2813-2820
- 101
Xiao J C, Ruck P, Adam A et al..
Small epithelial cells in human liver cirrhosis exhibit features of hepatic stem-like
cells: immunohistochemical, electron microscopic and immunoelectron microscopic findings.
Histopathology.
2003;
42
141-149
- 102
Naughton B A, Kolks G A, Arce J M et al..
The regenerating liver: a site of erythropoiesis in the adult Long-Evans rat.
Am J Anat.
1979;
156
159-167
- 103
Dornfest B S, Naughton B A, Kolks G A et al..
Recovery of an erythropoietin inducing factor from the regenerating rat liver.
Ann Clin Lab Sci.
1981;
11
37-46
- 104
Naughton B A, Gamba-Vitalo C, Naughton G K et al..
Granulopoiesis and colony stimulating factor production in regenerating liver.
Exp Hematol.
1982;
10
451-458
- 105 Ferrel L D, Theise N D, Scheuer P J. Acute and chronic viral hepatitis. In: MacSween
RNM, Burt AD, Portmann BC, et al. Pathology of the Liver. London; Churchill Livingstone
2002: 316-317
- 106
Tung J, Hadzic N, Layton M et al..
Bone marrow failure in children with acute liver failure.
J Pediatr Gastroenterol Nutr.
2000;
31
557-561
- 107
Cattral M S, Langnas A N, Markin R S et al..
Aplastic anemia after liver transplantation for fulminant liver failure.
Hepatology.
1994;
20
813-818
- 108
Kamiya A, Kinoshita T, Ito Y et al..
Fetal liver development requires a paracrine action of oncostatin M through the gp130
signal transducer.
EMBO J.
1999;
18
2127-2136
- 109
Paku S, Schnur J, Nagy P, Thorgeirsson S S.
Origin and structural evolution of the early proliferating oval cells in rat liver.
Am J Pathol.
2001;
158
1313-1323
- 110
Metcalf D.
The granulocyte-macrophage colony-stimulating factors.
Science.
1985;
229
16-22
- 111
Selden C, Chalmers S, Jones C et al..
Epithelial colonies cultured from human explant liver in subacute hepatic failure
exhibit hepatocyte, biliary epithelial and stem cell phenotypic markers.
Stem Cells.
2003;
21
624-631
Professor
Amar Paul Dhillon
Department of Histopathology, Royal Free and University College Medical School
Rowland Hill Street, London NW3 2PF, United Kingdom
Email: a.dhillon@rfc.ucl.ac.uk