mortality/aging
• mice die within 10 days following induction with pIpC
• cells induced with pIpC, when transplanted into irradiated wild-type mice, causes a lethal failure of hematopoiesis
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digestive/alimentary system
• following induction with pIpC, mice exhibit an increase in the number of apoptotic enterocytes at the base and along the crypts
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• following induction with pIpC, enterocytes are hyperchromatic with enlarged nuclei and loss of polarity
• following induction with pIpC, villus enterocytes are swollen with vacuolated cytoplasm and small pycnotic nuclei
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• following induction with pIpC, scattered crypts are diluted with necrotic cellular debris and lined by flattened epithelial cells
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• following induction with pIpC, mice exhibit villus atrophy with an increase in the number of apoptotic enterocytes at the base and along the crypts
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endocrine/exocrine glands
• following induction with pIpC, scattered crypts are diluted with necrotic cellular debris and lined by flattened epithelial cells
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small thymus
(
J:138468
)
• presumably due to spontaneous production of interferon in induced and un-induced mice
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hematopoietic system
small thymus
(
J:138468
)
• presumably due to spontaneous production of interferon in induced and un-induced mice
|
• following induction with pIpC, blood counts of mature hematopoietic cells is reduced
• cells induced with pIpC, when transplanted into irradiated wild-type mice, causes a lethal failure of hematopoiesis
|
• 4 days following induction with pIpC, bone marrow cellularity is reduced 10-fold due to 4.5-fold increase in apoptosis and decreased proliferation
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• in the one mouse that survived 10 days following induction with pIpC
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• in the one mouse that survived 10 days following induction with pIpC
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• following induction with pIpC, hematopoietic progenitor cells are not detected
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• following induction with pIpC, the neutrophil count is reduced to near zero by day 4
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• following induction with pIpC, lymphocyte counts decrease to a greater extent than in similarly treated mice without the cre transgene and do not recover
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• following induction with pIpC, monocyte counts decrease to a greater extent than in similarly treated mice without the cre transgene and do not recover
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• irregular following induction with pIpC
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• following induction with pIpC, red pulp size is reduced with a marked loss of hematopoietic cells
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• following induction with pIpC
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• following induction with pIpC, spleen cellularity is reduced 2-fold
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• following induction with pIpC, white pulp is moderately reduced with increased apoptosis of lymphocytes compared to in mice without the cre transgene
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immune system
small thymus
(
J:138468
)
• presumably due to spontaneous production of interferon in induced and un-induced mice
|
• following induction with pIpC, the neutrophil count is reduced to near zero by day 4
|
• following induction with pIpC, lymphocyte counts decrease to a greater extent than in similarly treated mice without the cre transgene and do not recover
|
• following induction with pIpC, monocyte counts decrease to a greater extent than in similarly treated mice without the cre transgene and do not recover
|
• irregular following induction with pIpC
|
• following induction with pIpC, red pulp size is reduced with a marked loss of hematopoietic cells
|
• following induction with pIpC
|
• following induction with pIpC, spleen cellularity is reduced 2-fold
|
• following induction with pIpC, white pulp is moderately reduced with increased apoptosis of lymphocytes compared to in mice without the cre transgene
|
cellular
• following induction with pIpC, mice exhibit an increase in the number of apoptotic enterocytes at the base and along the crypts
|