Plasticity of Schwann cells and pericytes in response to islet injury in mice

Diabetologia

Volumn 56, Issue 11, 2013, Pages 2424-2434

  Tang, Shiue Cheng ^a   Chiu, Yu Chen ^a   Hsu, Chia Tung ^a   Peng, Shih Jung ^a   Fu, Ya Yuan ^a,b  

^a NATIONAL TSING HUA UNIVERSITY   (Taiwan)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Gliosis; Insulitis; Islet; NOD mouse; Pericyte; Plasticity; Schwann cell; Streptozotocin

Indexed keywords

CELL MARKER;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTERIOLE; ARTERY BLOOD FLOW; ARTICLE; CELL AGGREGATION; CELL DAMAGE; CELL DENSITY; CELL STRUCTURE; CELL SURFACE; CONTROLLED STUDY; FEMALE; GLIOSIS; INSULITIS; LYMPHOCYTIC INFILTRATION; MOUSE; NERVE CELL NETWORK; NERVE CELL PLASTICITY; NONHUMAN; PANCREAS ISLET CELL; PERICYTE; PRIORITY JOURNAL; QUALITATIVE ANALYSIS; QUANTITATIVE ANALYSIS; SCHWANN CELL; TISSUE SECTION; VASCULARIZATION;

ANIMALS; FEMALE; ISLETS OF LANGERHANS; MALE; MICE; MICE, INBRED BALB C; MICROSCOPY, CONFOCAL; PANCREAS; PERICYTES; SCHWANN CELLS; STREPTOZOCIN;

EID: 84885869867     PISSN: 0012186X     EISSN: 14320428     Source Type: Journal    
DOI: 10.1007/s00125-013-2977-y     Document Type: Article

References (45)

1. Woods SC, Porte D Jr (1974) Neural control of the endocrine pancreas. Physiol Rev 54:596-619
2. Donev SR (1984) Ultrastructural evidence for the presence of a glial sheath investing the islets of Langerhans in the pancreas of mammals. Cell Tissue Res 237:343-348
3. Sunami E, Kanazawa H, Hashizume H, Takeda M, Hatakeyama K, Ushiki T (2001) Morphological characteristics of Schwann cells in the islets of Langerhans of the murine pancreas. Arch Histol Cytol 64:191-201
4. Hayden MR, Karuparthi PR, Habibi J et al (2008) Ultrastructure of islet microcirculation, pericytes and the islet exocrine interface in the HIP rat model of diabetes. Exp Biol Med (Maywood) 233:1109-1123
5. Richards OC, Raines SM, Attie AD (2010) The role of blood vessels, endothelial cells, and vascular pericytes in insulin secretion and peripheral insulin action. Endocr Rev 31:343-363
6. Fawcett JW, Asher RA (1999) The glial scar and central nervous system repair. Brain Res Bull 49:377-391
7. Pekny M, Nilsson M (2005) Astrocyte activation and reactive gliosis. Glia 50:427-434
8. Goritz C, Dias DO, Tomilin N, Barbacid M, Shupliakov O, Frisen J (2011) A pericyte origin of spinal cord scar tissue. Science 333:238-242
9. von Boyen GB, Steinkamp M, Reinshagen M, Schafer KH, Adler G, Kirsch J (2004) Proinflammatory cytokines increase glial fibrillary acidic protein expression in enteric glia. Gut 53:222-228
10. Cornet A, Savidge TC, Cabarrocas J et al (2001) Enterocolitis induced by autoimmune targeting of enteric glial cells: a possible mechanism in Crohn's disease? Proc Natl Acad Sci U S A 98:13306-13311
11. Costantini TW, Bansal V, Krzyzaniak M et al (2010) Vagal nerve stimulation protects against burn-induced intestinal injury through activation of enteric glia cells. Am J Physiol Gastrointest Liver Physiol 299:G1308-G1318
12. Vasina V, Barbara G, Talamonti L et al (2006) Enteric neuroplasticity evoked by inflammation. Auton Neurosci 126-127:264-272
13. Winer S, Tsui H, Lau A et al (2003) Autoimmune islet destruction in spontaneous type 1 diabetes is not beta-cell exclusive. Nat Med 9:198-205
14. Tsui H, Winer S, Chan Y et al (2008) Islet glia, neurons, and beta cells. Ann N Y Acad Sci 1150:32-42
15. Tsui H, Chan Y, Tang L et al (2008) Targeting of pancreatic glia in type 1 diabetes. Diabetes 57:918-928
16. Yantha J, Tsui H, Winer S et al (2010) Unexpected acceleration of type 1 diabetes by transgenic expression of B7-H1 in NOD mouse peri-islet glia. Diabetes 59:2588-2596
17. Teitelman G, Guz Y, Ivkovic S, Ehrlich M (1998) Islet injury induces neurotrophin expression in pancreatic cells and reactive gliosis of peri-islet Schwann cells. J Neurobiol 34:304-318
18. Nakamura M, Kitamura H, Konishi S et al (1995) The endocrine pancreas of spontaneously diabetic db/db mice: microangiopathy as revealed by transmission electron microscopy. Diabetes Res Clin Pract 30:89-100
19. Hayden MR, Karuparthi PR, Habibi J et al (2007) Ultrastructural islet study of early fibrosis in the Ren2 rat model of hypertension. Emerging role of the islet pancreatic pericyte-stellate cell. JOP 8:725-738
20. Papaccio G, Latronico MV, Pisanti FA, Federlin K, Linn T (1998) Adhesion molecules and microvascular changes in the nonobese diabetic (NOD) mouse pancreas. An NO-inhibitor (L-NAME) is unable to block adhesion inflammation-induced activation. Autoimmunity 27:65-77
21. Denis MC, Mahmood U, Benoist C, Mathis D, Weissleder R (2004) Imaging inflammation of the pancreatic islets in type 1 diabetes. Proc Natl Acad Sci U S A 101:12634-12639
22. Tuchin VV, Wang RK, Yeh AT (2008) Optical clearing of tissues and cells. J Biomed Opt 13:021101
23. Fu YY, Lin CW, Enikolopov G, Sibley E, Chiang AS, Tang SC (2009) Microtome-free 3-dimensional confocal imaging method for visualization of mouse intestine with subcellular-level resolution. Gastroenterology 137:453-465
24. Fu YY, Tang SC (2010) At the movies: 3-dimensional technology and gastrointestinal histology. Gastroenterology 139:1100-1105
25. Hama H, Kurokawa H, Kawano H et al (2011) Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain. Nat Neurosci 14:1481-1488
26. Liu YA, Chung YC, Pan ST et al (2013) 3-D imaging, illustration, and quantitation of enteric glial network in transparent human colon mucosa. Neurogastroenterol Motil 25:e324-e338
27. Fu YY, Lu CH, Lin CW et al (2010) Three-dimensional optical method for integrated visualization of mouse islet microstructure and vascular network with subcellular-level resolution. J Biomed Opt 15:046018
28. Chiu YC, Hua TE, Fu YY, Pasricha PJ, Tang SC (2012) 3-D imaging and illustration of the perfusive mouse islet sympathetic innervation and its remodelling in injury. Diabetologia 55:3252-3261
29. Ahren B (2012) Islet nerves in focus - defining their neurobiological and clinical role. Diabetologia 55:3152-3154
30. Fu YY, Peng SJ, Lin HY, Pasricha PJ, Tang SC (2013) 3-D imaging and illustration of mouse intestinal neurovascular complex. Am J Physiol Gastrointest Liver Physiol 304:G1-G11
31. Liu YA, Chung YC, Pan ST et al (2012) 3-D illustration of network orientations of interstitial cells of Cajal subgroups in human colon as revealed by deep-tissue imaging with optical clearing. Am J Physiol Gastrointest Liver Physiol 302:G1099-G1110
32. Liu YA, Chen Y, Chiang AS, Peng SJ, Pasricha PJ, Tang SC (2011) Optical clearing improves the imaging depth and signal-to-noise ratio for digital analysis and three-dimensional projection of the human enteric nervous system. Neurogastroenterol Motil 23:e446-e457
33. Bergers G, Song S (2005) The role of pericytes in blood-vessel formation and maintenance. Neuro Oncol 7:452-464
34. Ravnic DJ, Jiang X, Wolloscheck T et al (2005) Vessel painting of the microcirculation using fluorescent lipophilic tracers. Microvasc Res 70:90-96
35. Fu YY, Tang SC (2010) Optical clearing facilitates integrated 3D visualization of mouse ileal microstructure and vascular network with high definition. Microvasc Res 80:512-521
36. Taylor-Fishwick DA, Bowman A, Korngiebel-Rosique M, Vinik AI (2008) Pancreatic islet immunoreactivity to the Reg protein INGAP. J Histochem Cytochem 56:183-191
37. Carl Zeiss Microimaging GmbH (2009) Visualizing the architecture of cells and tissues. Brochures for laser scanning microscopy. Available from http://microscopy.zeiss.com/microscopy/en-gb/downloads/brochure-downloads.html? catalog=biowhitepaper. Accessed 14 June 2013
38. Sandler S, Jansson L (1985) Vascular permeability of pancreatic islets after administration of streptozotocin. Virchows Arch A Pathol Anat Histopathol 407:359-367
39. Papaccio G (1993) Insulitis and islet microvasculature in type 1 diabetes. Histol Histopathol 8:751-759
40. Beppu H, Maruta K, Kurner T, Kolb H (1987) Diabetogenic action of streptozotocin: essential role of membrane permeability. Acta Endocrinol (Copenh) 114:90-95
41. Enghofer M, Usadel KH, Beck O, Kusterer K (1997) Superoxide dismutase reduces islet microvascular injury induced by streptozotocin in the rat. Am J Physiol 273:E376-E382
42. Papaccio G, Baccari GC, Strate C, Linn T (1994) Pancreatic duct inflammatory infiltration in the nonobese diabetic (NOD) mouse. J Anat 185:465-470
43. Tsui H, Winer S, Jakowsky G, Dosch HM (2003) Neuronal elements in the pathogenesis of type 1 diabetes. Rev Endocr Metab Disord 4:301-310
44. Meyerzu Horste G, Hu W, Hartung HP, Lehmann HC, Kieseier BC (2008) The immunocompetence of Schwann cells. Muscle Nerve 37:3-13
45. Wekerle H, Schwab M, Linington C, Meyermann R (1986) Antigen presentation in the peripheral nervous system: Schwann cells present endogenous myelin autoantigens to lymphocytes. Eur J Immunol 16:1551-1557