Sclerocorneal limbal stem cell autograft transplantation in dogs

Transplante autógeno de células tronco do limbo esclerocorneal em cães

VETERINARY MEDICINE

Sclerocorneal limbal stem cell autograft transplantation in dogs

Transplante autógeno de células tronco do limbo esclerocorneal em cães

A.T.J. Brunelli^I; F.A.M. Vicente^I; F. Chahud^II; A.P. Oriá^I; A.A. Bolzan^I; C.F. Campos^I; F.A. Doria Neto^I; J.L. Laus^III,*

^IAluno de pós-graduação - FCAV-UNESP – Jaboticabal, SP

^IIAluno de pós-graduação - USP – Ribeirão Preto, SP

^IIIFaculdade de Ciências Agrárias e Veterinárias - UNESP Via de Acesso Prof. Paulo Donato Castellane, s/n 14884-900 - Jaboticabal, SP

ABSTRACT

The effects of sclerocorneal limbal stem cell autograft transplantation in dogs with corneal wounds were studied. Eighteen dogs were divided in two groups (GI and GII). The animals of GI (n=12) underwent limbal transplantation 30 days after the destruction of limbal stem cells. The dogs of GII (n=6) only underwent destruction of stem cells (control group). Light microscopy examination of the right eye was performed on days 3, 7, 14, 30, 60, and 120 after limbal transplantation (GI), and on days 33, 37, 44, 60, 90, and 150 after limbal destruction (GII). Results showed a complete destruction of limbal stem cells with loss of corneal transparency. Limbal transplantation prevented conjunctivalization in grafted area. Corneal vascularization and a 360º corneal conjunctivalization were noted in the control dogs (GII). Corneal transparency was restored from day 60^th after surgery. Histological examination did not distinguish the transition between the graft and the normal corneal epithelium at anytime. Goblet cells were found in control animals (GII) on 33, 37, 60, and 150 days, whereas a single grafted dog (GI) presented a few goblet cells on day 60^th post-transplantation. Limbal autograft transplantation was effective in restoring corneal clarity with no development of ocular complications.

Keywords: dog, stem cells, limbus, autograft transplantation

RESUMO

Avaliaram-se os efeitos do transplante de células tronco autógenas do limbo esclerocórneo de cães, sobre lesões córneo-limbais. Empregaram-se 18 cães, distribuídos em dois grupos, GI e GII. Nos animais do GI (n=12), foram realizados transplantes de limbo, após 30 dias da destruição das células tronco-límbicas. Nos do GII (n=6), realizou-se apenas a destruição do limbo (controle). Aos 3, 7, 15, 30, 60 e 120 dias do transplante de limbo (GI) e aos 33, 37, 45, 60, 90 e 150 dias da destruição do limbo (GII), os olhos foram coletados por enucleação subconjuntival, para estudos em microscopia de luz. A destruição do limbo resultou em completa excisão das células tronco, com perda da transparência corneal. O transplante do limbo evitou a conjuntivalização na área em que foi realizado. Os animais do grupo-controle manifestaram conjuntivalização em 360º e vascularização corneal. Na anatomopatologia, em nenhum dos períodos foi possível distinguir o enxerto do epitélio corneal normal. As células caliciformes foram observadas nos animais do GII, nos períodos 33, 37, 60, 150 dias. No GI, apenas um cão manifestou células caliciformes de forma discreta, aos 60 dias do transplante. O transplante autógeno foi eficiente em possibilitar a melhoria da transparência córnea, sem intercorrências oculares.

Palavras-chave: cão, células tronco, limbo, transplante autógeno

INTRODUCTION

Stem cells are responsible for tissue replacement and regeneration (Akped and Foster, 1999). They are essential to maintain the integrity of corneal surface, by promoting its renewal in healthy states and reepithelialization in wound healing processes (Swift et al., 1996; Haamann et al., 1998; Dua and Azuara-Blanco, 1999).

Stem cells are believed to be located in the limbal basal epithelium (Chung et al., 1992). The exact location of corneal stem cells was proved by using monoclonal antibodies (Schermer et al., 1986; Chung et al., 1992), and by stimulating corneal and limbal cells with a tumor-promoting agent (Cotsarelis et al., 1989). Also, impression cytology and histology were used for this purpose (Puangsricharern and Tseng, 1995).

Limbal deficiency or loss of stem cells is characterized by a reduction of proliferative capacity, resulting in abnormal corneal surface (Akped and Foster, 1999). In such occasions, there is growth of the conjunctival epithelium onto the corneal surface (conjunctivalization), as well as chronic inflammation, superficial vascularization, calcification, ulceration, melting and perforation of the cornea (Swift et al., 1996; Tseng and Tsubota, 1997; Dua and Azuara-Blanco, 1999; Dua and Azuara-Blanco, 2000). When corneal surface is covered by conjunctival epithelium, goblet cells can be seen in this specialized part of the fibrous tunic (Dua, 1998; Schwab, 1999).

The symptoms of limbal deficiency may include photophobia, decreased vision, tearing, blepharospasm, and redness (Dua and Azuara-Blanco, 1999). Untreated limbal and corneal injuries may result in persistent epithelial defects, conjunctivalization of the cornea, destructive lesions of the basal membrane, and perforation of the cornea (Chan and Foster, 1999).

Surgical procedures are required to treat severe lesions and restore the integrity of ocular surface (Coster et al., 1995). Either total or partial autograft transplantation is recommended in patients with limbal stem cell deficiency. When autograft transplantation is not possible, limbal allograft can be alternatively used (Coster et al., 1995; Dua and Azuara-Blanco, 1999).

Taking into account that partial or total destruction of the sclerocorneal limbal stem cells results in very significant corneal alterations, this study aimed at investigating the proposal of an experimental model of limbal destruction, as well as its consequences and the effects of limbal autograft transplantation in dogs.

MATERIAL AND METHODS

Eighteen adult healthy mixed-breed dogs of either sex were used. The bioethical handling of animals followed the rules given by the Association for Research in Vison and Ophthalmology according to the Nüremberg code (Goldim, 1995) and the Comissão de Ética na Experimentação Animal da Faculdade de Ciências Agrárias e Veterinárias - UNESP – Jaboticabal, SP.

Food and water were withheld for an 8-hour period prior to the operative procedures. Animals were pre-medicated with levomepromazine¹, 1mg/kg IV, followed by anesthetic induction with sodium thiopental² 12.5mg/kg IV. A halogenated anesthetic agent³ diluted in oxygen was delivered via a closed anesthetic circuit to maintain anesthesia in the third plane of the third stage (Guedel, 1952).

Only one surgeon performed all the procedures. The destruction of stem cells was performed in only one eye (right eye). For such, a sterile cotton tip wet with n-heptanol solution⁴ was applied to the eye in a circular fashion for 120 seconds, beginning centrally and extending to the bulbar conjunctiva to cause total deepithelialization. The area was immediately rinsed with sterile saline solution⁵ for two minutes to remove the excess of n-heptanol. Since the procedure alone is not able to completely remove stem cells, a 360º lamellar keratectomy was employed as an ancillary method (Tsai et al., 1990)

Keratectomy was started after routine preparation, protection, and antiseptic treatment of the operative field with 10% buffered polyvinylpyrrolidone – iodine solution (PVPI)⁶ diluted in saline solution⁵ (1/50). Under six-time magnification provided by the operating microscope⁷, the limbal zone was excised in a 360º lamellar pattern, removing approximately 2mm of the cornea and 3mm of the conjunctiva. To allow this procedure, a #66 Beaver blade⁸ and Barraquer scissors were used. The ocular surface was systematically irrigated with sterile 0.9% saline solution⁵ during the procedure. After surgery, fluorescein test ⁹was performed to delimit the injured area.

After the surgical maneuvers, the animals wore Elizabethan collars. All dogs were prophylactically given topical tobramicine¹⁰ and nonsteroidal anti-inflammatory flurbiprofen¹¹, both at regular non-coincident 6-hour intervals for 14 consecutive days. To reduce ciliary spasm, 1% atropine eyedrops¹² was instilled at 12-hour intervals for three days, followed by use every 24 hours for further three days. It was also instituted analgesic and anti-inflammatory therapy with oral meloxicam¹³ 0.1mg/kg of body weight, daily for five days.

One month after limbal destruction, the animals were divided into two groups. GI was composed of 12 dogs that were submitted to limbal autograft transplantation, and GII was composed of six dogs used as control.

After preparation and protection of the operating field, limbal stem cells were collected from the fellow eye (left eye). Under a 6-time magnification provided by an operating microscope⁷, superficial lamellar dissection of the peripheral cornea was carried out to remove two 3-mm-conjunctival strips involving the limbal circumference of 11-13 and 17-19 o’clock (Fig. 1A). Grafts were stored at room temperature in a sterile recipient containing autologous serum for the least required time until transplantation was performed.

The graft was transplanted to the recipient eye shortly after its excision. After preparation and protection of the surgical area, the limbal graft was transferred to the recipient bed and sutured at the 11-to-13-o’clock and 17-to-19-o’clock positions, extending 2mm into the cornea and 3mm beyond the conjunctiva (Tan et al., 1996) (Fig. 1B and 1C). The grafts were secured to the bulbar conjunctiva and cornea with seven non-penetrating interrupted 9-0 monofilament nylon sutures¹⁴. A distance of 1mm was left between sutures (Fig. 1D).

Every dog wore an Elizabethan collar after surgery. Topical tobramicine¹⁰ and nonsteroidal anti-inflammatory flurbiprofen¹¹ were used four times a day for the first seven days, followed by topical trobramicine and dexametasone eyedrops and ointments¹⁵ four times daily for the next seven days. Atropine eyedrops¹² was used at 12-hour intervals for three days and every day for further three days. Also, dogs were given Buprenorfin¹⁶, 3µg/kg IM, for three consecutives days and meloxican¹³, 0.1mg/kg orally every 24 hours for five days.

Each dog was daily examined by the same person for any signs of blepharospasm, ocular discharge, conjunctival injection, chemosis, corneal neovascularization, corneal opacity and pigmentation, and conjunctivalization. The results were analyzed under subjective quantitative criteria. The dogs were daily examined at the slit lamp¹⁷, applanation tonometry¹⁸, Schirmer’s tear test¹⁹, and fluorescein test⁹. Fisher’s exact test was used to analyze clinical signs at a significance level of 5% (P< 0.05).

Histological examination was performed on days 3, 7, 14, 30, 60, and 120 after limbal transplantation in GI dogs, and on days 33, 37, 44, 60, 90, and 150 after limbal destruction in animals of GII. Each evaluation included two dogs of GI and one dog of GII.

RESULTS

No alterations were observed in intraocular pressure and Schirmer’s tear test after limbal ablation. Corneal vascularization reached up to 2mm beyond the limbus in 83.3% of the animals and 4mm beyond the limbus in 16.7% of the dogs seven days after limbal destruction. Corneal vascularization was seen in every animal on day 14^th. Neovessels reached 2mm, 4mm, and 6mm beyond the limbus in 33.3%, 33.3%, and 33.3% of the dogs, respectively.

Thirty days after injury, vascularization was still seen in all animals. Most of them (72.2%) had 6-mm neovessels extending from the limbus into central cornea. In 27.8% of the dogs, however, vessels were not 4mm beyond the limbus.

Corneal granulation tissue developed seven days after ablation, being mild in 22.2%, moderate in 11.1%, and severe in 22.2% of the dogs. No granulation tissue was seen in 44.4% of the animals. On day 14^th, granulation was absent in 33.3% of the animals, mild in 16.7%, moderate in 5.6%, and severe in 50%. On day 30^th, most dogs did not show any granulation tissue (61.1%), whereas in 16.7%, 5.6%, and 16.7% of the animals, it was observed in mild, moderate, and severe grades, respectively.

Severe keratitis was observed in 11.1% of the cases on day 14^th. In such animals, the most representative findings were mucopurulent ocular discharge, deep corneal neovessels, severe corneal edema, granulation, and thickening of the cornea. Such signs tended to regression on day 30^th. Table 1 shows the results regarding ocular discharge, blepharospasm, chemosis, conjunctival injection, pigmentation, conjunctivalization, and fluorescein test.

No systemic or ocular complications were observed in animals of GI. There was no dehiscence, infection, limbal graft rejection, or any significant manifestations besides those usually observed in similar procedures. None of the animals developed either ulcerative keratitis or granulation. Also, the results of intraocular pressure and Schirmer’s tear test were within the normal range in all times.

Three days after limbal transplantation, 25% of GI dogs had developed corneal vascularization up to 2mm beyond the limbus. In 58.3% of the animals, neovessels reached up to 6mm beyond the limbus, whereas in the remaining dogs (25%), it was only observed vessels on central corneal. Regarding the animals of control group (GII), corneal neovascularization up to 2mm and 6mm beyond the limbus was seen in 16.7% and 67.7% of the dogs, respectively. In the remaining 16.7%, neovessels were only observed on central corneal.

After seven days, neovessels reached up to 2mm in 40% of GI dogs and 20% of GII dogs. In 50% of GI animals and 60% of GII animals, the vessels reached up to 6mm beyond the limbus. Central corneal neovascularization was seen in 10% of GI dogs and 20% of GII.

Fourteen days after limbal transplantation, 37.5% of GI dogs and 25% of GII dogs had neovessels reaching up to 2mm beyond the limbus, whereas in 50% of GI and GII dogs, neovascularization reached up to 6 mm. In the remaining 12.5% of GI dogs and 25% of GII dogs, neovascularization was located on central cornea.

On day 30^th, no vascularization was seen in 16.7% of GI dogs. Neovessels reaching up to 2mm and 6mm beyond the limbus was found in 50% and 16.66% of the animals, respectively. Vessels were equally distributed in dogs of GII (2mm, 6mm, and on central cornea).

On day 60^th, neovascularization reached 2mm and 6mm beyond the limbus in 50% and 25% of GI dogs, respectively. In the remaining 25%, vessels were located on central cornea. In GII, 50% of the dogs had neovessels reaching up to 2mm beyond the limbus, whereas in 50% they reached 6mm beyond the limbus.

On day 120^th, neovessels reached 2mm beyond the limbus in 50% of GI dogs, whereas the remaining 50% had neovessels on central corneal. In every animal of control group the vessels reached 2mm beyond the limbus.

Animals of group GI did not exhibit conjunctivalization at the transplantation site. In the control group without transplantation, however, a 360º corneal conjunctivalization was observed.

Results of ocular discharge, blepharospasm, chemosis, conjunctival injection, pigmentation, conjunctivalization, and fluorescein test are shown in Tables 2 and 3. The clinical evolution is presented in Fig. 2 (A, B, ^C, ^D, ^E, ^F, ^G, ^H).

No alterations in intraocular pressure and Schirmer’s tear test occured. Seven days after surgical procedure, all dogs had developed corneal neovascularization. On day 14^th, neovessels were limited to the wound area in most dogs (87.5%). In contrast, neovascularization was not seen in the remaining 12.5%. Thirty days after injury, vascularization was present in only 33.3% of the animals, whereas in 66.7% it was absent. At the end of two months, 50% of the dogs had superficial corneal vessels reaching 2mm beyond the limbus. On day 120^th, however, no corneal vessels were seen anymore. Results of ocular discharge, blepharospasm, chemosis, conjunctival injection, pigmentation, conjunctivalization, and fluorescein test are shown in Table 4.

Results of data analysis by Fisher’s test are shown in Table 5. Statistical analysis was not carried out on day 120^th due to the reduced number of animals in either group (two dogs in GI and one dog in GII).

In GI, the transition between limbal autograft and normal corneal epithelium at anytime could not be distinguished. It was therefore defined by the localization of sutures.

In GI, the epithelium healed within three days of transplantation, although focal irregularities due to its thickness and to epithelial cells hyperplasia were present. Goblet cells were not observed in this area. Thirty-three days after limbal destruction (GII), corneal thickness decreased in both peripheral and central cornea, and a reduced number of goblet cells was seen in corneal epithelium.

Seven days after transplantation (GI) and 37 days after limbal ablation (GII), epithelial hyperplasia was noted in central cornea of GI animals, whereas in GII, an intact epithelium with normal thickness was observed. Goblet cells were not seen in GI corneas. In contrast, a moderate number of goblet cells were found in the peripheral cornea of GII dogs.

Although focal peripheral corneal irregularities were seen on day 14^th after transplantation, a healed epithelium was noted in every animal of GI. Also, no goblet cells were found in any dog except in one, in which they were mildly distributed along the corneal periphery. Forty-four days after limbal destruction (GII), a normally thickened epithelium was found, and no corneal goblet cells were noted.

Thirty days after transplantation, the dogs of GI showed thickened areas in both peripheral and central cornea, and goblet cells were absent in the corneal epithelium. Sixty days after injury, corneal periphery exhibited a reduced epithelial layer in the control group without transplantation (GII). Also, goblet cells were moderately present in peripheral and central corneal epithelia.

Later (on 60^th and 120^th days), epithelial hyperplasia was observed in every dog of either group. In only one animal of GI, goblet cells were found in the peripheral corneal epithelium. The histologic examination is presented in Fig. 3 (A, B, ^C, ^D, ^E, and ^F).

DISCUSSION

Experimental limbal destruction is performed to induce corneal alterations similar to accidental lesions and to further study effective therapeutic alternatives. Both chemical debridement (n-heptanol, iodine, sodium hydroxide solution) and mechanical debridement (corneal scarification, superficial keratectomy) have been described in rabbits, guinea pigs, and primates (Hirst et al., 1981; Kruse et al., 1990).

Chemical debridement with n-heptanol aims at removing corneal epithelium without damaging the basal layer (Hirst et al., 1981; Kruse et al., 1990). Kenyo and Tseng (1989), however, showed that n-heptanol alone did not remove the entire limbal epithelium. To extinguish stem cells completely, limbal epithelium might be removed thoroughly to avoid the mobilization of surrounding transient amplifying cells and stem cells (Chen and Tseng, 1990).

In a pilot study of our laboratory, n-heptanol debridement for 60 seconds followed by lamellar keratectomy failed to cause severe corneal alterations, resulting in mild edema and vascularization, and rapid epithelial healing. Therefore, it was observed that n-heptanol shold be applied to the eye for 120 seconds, which resulted in a thorough removal of stem cells.

Although Huang and Tseng (1988) and Kenyon and Tseng (1989) reported that in the absence of limbal epithelium corneal wound healing becomes less efficient, characterized by recurrent erosions. This finding was observed in this study. Corneal healing was achieved within 20 days after limbal destruction, without recurrent erosions over 150 days post-ablation.

Conjunctival epithelial ingrowth onto the cornea is dependent on the variable extent of the ocular lesion and removal of stem cells (Chen and Tseng, 1990; Tsai et al., 1990). Most times conjunctivalization is accompanied by corneal vascularization (TSAI et al., 1990). In this study, conjunctivalization and vascularization started within seven days after limbal destruction, and progressed in every animal, over 30 days after wounding.

After limbal autograft transplantation, Tsai et al. (1990) found corneal vascularization in four of five rabbits, on 120^th day of evaluation. In the current report, vessels extending 2mm beyond the limbus, were observed in 50% of the dogs, whereas in the remaining, they were noted in central cornea. Fargerholm and Lisha (1999) suggested that the regression of vessels might indicate an interaction between corneal epithelium and stroma that is not observed when conjunctivalization is present.

Intense pigmentation was seen in the animals of group GII 150 days after limbal destruction. In the group of limbal transplantation, mild-to-absent pigmentation was noted. When present, it was located next to the limbal area not covered by the grafts.

Limbal stem cells are recognized to play a vital role in corneal epithelial cell renewal. Therefore, ocular surface damages may develop in their absence (Tseng and Tsubota, 1997). In this study, exuberant granulation was especially seen, on day 14^th after limbal ablation, with regression by day 30. Tsai et al. (1990) observed granulation at the end of the fourth month after limbal injury, in rabbits, however, in the dogs of this study, in which granulation lasted for a maximum of 46 days after limbal destruction, that event could not be documented.

Conjunctival goblet cells were found on corneal epithelium. The presence of goblet cells substantiates that conjunctivalization occurred following limbal destruction. Fagerholm and Lisha (1999) showed that in the human being eye, goblet cells are found on corneal epithelium after chemical burns. In the current study, goblet cells were documented 33 days after limbal ablation, particularly in control group animals, and in a single grafted dog. Fagerholm and Lisha (1999) further reported that the success of limbal transplantation might be confirmed by the absence of goblet cells in the corneal epithelium.

After transplantation, corneal and limbal epithelial healing was achieved between three and 21 days. This finding is in agreement with studies by Kenyo and Tseng (1989) and Tan et al. (1996). In human beings, Fagerholm and Lisha (1999) reported epithelial proliferation at two weeks post-transplantation. In dogs, however, healed corneal epithelium was noted three days post-transplantation, although hyperplasia was also present.

As reported by Dua and Azuara-Blanco (2000), no complications occurred in donor eyes. Corneal edema, vascularization, and conjunctivalization started regressing 60 days after surgery and complete regression was observed up to 60 days later. Although Morgan and Murray (1996) reported corneal micro-perforations in donor eyes of human beings such complication was not noticied in this research.

CONCLUSIONS

The dog model of total limbal destruction is feasible and reliable in producing severe ocular surface wounds, resulting in loss of corneal clarity. Limbal autograft transplantation was effective in restoring the corneal transparency with no ocular complications. The absence of complications in the donor eyes of dogs is an evidence of the advantages and efficacy of limbal autograft transplantation, in managing stem cell deficiency, after mechanical trauma or chemical injury.

ACKNOWLEDGMENT

The authors thank to Dr. Gener Tadeu Pereira for performing the statistical analysis. The Programa de Internacionalização da Pesquisa da UNESP. Research supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico – CNPq.

Recebido em 18 de novembro de 2005

Aceito em 13 de agosto de 2007

• AKPED, E.K.; FOSTER, C.S. Limbal stem cells transplantation. Int. Ophthalmol. Clin, v.39, p.71-81, 1999.
• CHAN, R.Y.; FOSTER, C.S. A step-wise pproach to ocular surface rehabilitation in patients with ocular inflammatory disease. Int. Ophthalmol. Clin., v.39, p.83-107, 1999.
• CHEN, J.J.Y.; TSENG, S.C.G. Corneal epithelial wound healing in partial limbal deficiency. Invest. Ophthalmol. Visual Sci., v.31, p.1301-1314, 1990.
• CHUNG, E.H.; BUKUSOGLU, G.; ZIESKE, J.D. Localization of corneal epithelium stem cells in the developing rat. Invest. Ophthalmol. Visual Sci, v.33, p.2199-2206, 1992.
• COSTER, D.J.; AGGARWAL, R.K.O.; WILLIAMS, K.A. Surgical management of ocular surface disorders using conjunctival and stem cells allografts. Br. J. Ophthalmol., v.79, p.977-982, 1995.
• COTSARELIS, G.; CHEN, S.Z.; LAVKER, R.M. Existence of slow-cycling limbal epithelial basal cells that can be preferentially stimulated to proliferate: implications on epithelial stem cells. Cell, v.57, p.201-209, 1989.
• DUA, H.S. The conjuntival in corneal epithelial wound healing. Br. J. Ophthalmol., v.82, p.1407-1411, 1998.
• DUA, H.S.; AZUARA-BLANCO, A. Allo-limbal transplantation in patients with limbal stem cell deficiency. Br. J. Ophthalmol., v.83, p.414-419, 1999.
• DUA, H.S.; AZUARA-BLANCO, A. Limbal stem cells of corneal epithelium Surv. Ophthalmol., v.44, p.415-425, 2000.
• FAGERHOLM, P.; LISHA, G. Corneal stem cells grafting after chemical injury. Acta Ophthalmol. Scand, v.77, p.165-169, 1999.
• GOLDIM, J. R. Pesquisa em saúde e direitos dos animais Porto Alegre: HCPA, 1995. 28p.
• GUEDEL, A. E. (Ed). Inhalation anesthesia 2.ed. New York: Macmillian, 1952.
• HAAMANN, P.; JENSEM, O.M.; SCHIMIDT, P. Limbal autograft transplantation. Acta Ophthalmol. Scand, v.76, p.117-118, 1998.
• HIRST, L.W.; KENYON, K.R.; FOGLE, J.A. et al. Comparative studies of corneal surface injury in the mankey and rabbit. Arch. Ophthalmol, v.99, p.1066-1073, 1981.
• HUANG, A.J.W.; TSENG, S.C.G. Corneal epithelial wound healing in the absence of limbal epithelium. ARVO Abstracts. Invest. Ophthalmol. Visual Sci, v.29, suppl., p.190, 1988.
• KENYON, K.R.; TSENG, S.C.G. Limbal autograft transplantation for ocular surface disorders. Ophthalmology, v.96, p.709-723, 1989.
• KRUSE, F.E.; CHEN, J.J.Y.; TSAI, R.J.F. et al. Conjunctival transdifferentiation is due to the incomplete removal of limbal basal epithelium. Invest. Ophthalmol. Visual Sci, v.36, p.1903-1913, 1990.
• MORGAN, S.; MURRAY, A. Limbal auto-transplantation in the acute ang chronic phases of severe chemical injuries. Eye, v.10, p.349-354, 1996.
• PUANGSRICHARERN, V.; TSENG, S. C. G. Citology evidence of corneal diseases with limbal stem cells deficiency. Ophthalmology, v.102, p.1476-1485, 1995.
• SCHERMER, A.; GALVIN, S.; SUN, T.T. Differentiation-related expression of a major 64K corneal keratin in vivo and in culture suggests limbal location of corneal epithelial stem cells. J. Cell Biol, v.103, p.49-62, 1986.
• SCHWAB, I.R. Cultured corneal epithelia for ocular surface disease. Transact. Am. Soc., v.97, p.891-939, 1999.
• SWIFT, G.J.; AGGARWAL, R.K.; DAVIS, G.J. et al. Survival of rabbit limbal stem cell allografts. Transplatation, v.62, p.568-574, 1996.
• TAN, D.T.; FICKER, L.A.; BUCKLEY, R.J. Limbal transplantation. Ophthalmology, v.103, p.29-36, 1996.
• TSAI, R.J.; SUN, T.T.; TSENG, S.C.G. Comparison of limbal and conjunctival autograft transplantion in corneal surface reconstruction in rabbits. Ophthalmology, v.97, p.446-455, 1990.
• TSENG, S.C.G.; TSUBOTA, K. Important concepts for treating ocular surface and tear disorders. Am. J. Ophthalmol, v.124, p.825-835, 1997.

1

Neozine? - Laboratório Rhodia

2

Thiopentax® - Laboratório Cristália

3

Fluotane® - Laboratório Astrazeneca

4

N-heptanol solution - Merck-Achuchardt

5

Sterile 0.9% saline solution – JP Indústria Farmacêutica S.A.

6

Marcodine Tópico® - Innovatec – Divisão Cristália

7

Microscope MC-M900-D.F. Vasconcellos S.A.

8

#66 Beaver blade® Alcon Surgical

9

Ophthalmos® - Ophthalmos Ind. Com. Prod. Farm. Ltda.

10

Tobrex® - Alcon Laboratórios do Brasil

11

Ocufen® - Laboratório Allergan-Frumtost

12

Atropine 1%® - Laboratório Allergan-Lok

13

Maxican® Laboratório Ouro Fino

14

Mononylon 9-0 – Ethicon S.A.

15

Tobramax® colírio e pomada – Alcon Laboratórios do Brasil

16

Temgesi® - Schering Ploug

17

Portable stit-lamp SL-14 - Kowa

18

Tono-pen XL, Mentor®

19

Schimer's Tear test – Ophtalmos Ind. Com. Prod. Farma. Ltda.

Publication Dates

• Publication in this collection
  19 Dec 2007
• Date of issue
  Oct 2007

History

• Accepted
  13 Aug 2007
• Received
  18 Nov 2005