Murine spleen tissue regeneration from neonatal spleen capsule

Jonathan Kah Huat Tan, Takeshi Watanabe

Research output: Contribution to conferenceOtherResearch

Abstract

Spleen is a secondary lymphoid organ which filters antigens circulating in blood. The importance of spleen as an immune tissue is highlighted by its removal which leads to an increased risk of overwhelming postsplenectomy infection (OPSI). For this reason, spleen auto-transplants are commonly performed to preserve splenic tissue, owing to the remarkable capacity for spleen to regenerate.

In previous experimental models, spleen from day 15 mouse embryos were shown to regenerate following transplantation under the kidney capsule (Glanville, 2009). In this study, murine spleen tissue was shown to regenerate from neonatal spleen capsule alone. Spleen capsules isolated from 3 day-old mice and transplanted under the kidney capsule of adult recipients regenerated splenic tissue after 4 weeks, displaying structures including red and white pulp, T and B cell compartments, follicular dendritic cell networks, marginal zones and conduit structures. Regenerated spleens also demonstrated functional capacity supporting antibody class switching and affinity maturation.

Transplantation efficiency was dependent on donor age with capsules isolated from 3 day-old mice more successful than 8 day-old ¬¬spleen capsules. In contrast, recipient age did not appear to be important with transplantations equally successful from both 6 and 30 week-old recipients. We are now attempting to identify stromal cells in spleen capsule that initiate spleen neogenesis. Overall, these results are expected to lead towards development of artificial spleen.
Original languageEnglish
Publication statusPublished - 17 Dec 2010
Externally publishedYes
EventThe 2nd Workshop of Synthetic Immunology - Kyoto University, Kyoto, Japan
Duration: 17 Dec 201018 Dec 2010

Workshop

WorkshopThe 2nd Workshop of Synthetic Immunology
CountryJapan
CityKyoto
Period17/12/1018/12/10

Fingerprint

Capsules
Regeneration
Spleen
Transplantation
Follicular Dendritic Cells
Immunoglobulin Class Switching
Antibody Affinity
Immunoglobulin Isotypes
Stromal Cells
Kidney Transplantation
B-Lymphocytes
Theoretical Models
Embryonic Structures
T-Lymphocytes
Transplants
Kidney
Antigens

Cite this

Tan, J. K. H., & Watanabe, T. (2010). Murine spleen tissue regeneration from neonatal spleen capsule. The 2nd Workshop of Synthetic Immunology, Kyoto, Japan.
Tan, Jonathan Kah Huat ; Watanabe, Takeshi. / Murine spleen tissue regeneration from neonatal spleen capsule. The 2nd Workshop of Synthetic Immunology, Kyoto, Japan.
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Tan, JKH & Watanabe, T 2010, 'Murine spleen tissue regeneration from neonatal spleen capsule' The 2nd Workshop of Synthetic Immunology, Kyoto, Japan, 17/12/10 - 18/12/10, .

Murine spleen tissue regeneration from neonatal spleen capsule. / Tan, Jonathan Kah Huat; Watanabe, Takeshi.

2010. The 2nd Workshop of Synthetic Immunology, Kyoto, Japan.

Research output: Contribution to conferenceOtherResearch

TY - CONF

T1 - Murine spleen tissue regeneration from neonatal spleen capsule

AU - Tan, Jonathan Kah Huat

AU - Watanabe, Takeshi

PY - 2010/12/17

Y1 - 2010/12/17

N2 - Spleen is a secondary lymphoid organ which filters antigens circulating in blood. The importance of spleen as an immune tissue is highlighted by its removal which leads to an increased risk of overwhelming postsplenectomy infection (OPSI). For this reason, spleen auto-transplants are commonly performed to preserve splenic tissue, owing to the remarkable capacity for spleen to regenerate.In previous experimental models, spleen from day 15 mouse embryos were shown to regenerate following transplantation under the kidney capsule (Glanville, 2009). In this study, murine spleen tissue was shown to regenerate from neonatal spleen capsule alone. Spleen capsules isolated from 3 day-old mice and transplanted under the kidney capsule of adult recipients regenerated splenic tissue after 4 weeks, displaying structures including red and white pulp, T and B cell compartments, follicular dendritic cell networks, marginal zones and conduit structures. Regenerated spleens also demonstrated functional capacity supporting antibody class switching and affinity maturation.Transplantation efficiency was dependent on donor age with capsules isolated from 3 day-old mice more successful than 8 day-old ¬¬spleen capsules. In contrast, recipient age did not appear to be important with transplantations equally successful from both 6 and 30 week-old recipients. We are now attempting to identify stromal cells in spleen capsule that initiate spleen neogenesis. Overall, these results are expected to lead towards development of artificial spleen.

AB - Spleen is a secondary lymphoid organ which filters antigens circulating in blood. The importance of spleen as an immune tissue is highlighted by its removal which leads to an increased risk of overwhelming postsplenectomy infection (OPSI). For this reason, spleen auto-transplants are commonly performed to preserve splenic tissue, owing to the remarkable capacity for spleen to regenerate.In previous experimental models, spleen from day 15 mouse embryos were shown to regenerate following transplantation under the kidney capsule (Glanville, 2009). In this study, murine spleen tissue was shown to regenerate from neonatal spleen capsule alone. Spleen capsules isolated from 3 day-old mice and transplanted under the kidney capsule of adult recipients regenerated splenic tissue after 4 weeks, displaying structures including red and white pulp, T and B cell compartments, follicular dendritic cell networks, marginal zones and conduit structures. Regenerated spleens also demonstrated functional capacity supporting antibody class switching and affinity maturation.Transplantation efficiency was dependent on donor age with capsules isolated from 3 day-old mice more successful than 8 day-old ¬¬spleen capsules. In contrast, recipient age did not appear to be important with transplantations equally successful from both 6 and 30 week-old recipients. We are now attempting to identify stromal cells in spleen capsule that initiate spleen neogenesis. Overall, these results are expected to lead towards development of artificial spleen.

M3 - Other

ER -

Tan JKH, Watanabe T. Murine spleen tissue regeneration from neonatal spleen capsule. 2010. The 2nd Workshop of Synthetic Immunology, Kyoto, Japan.