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Like Wild-Type (WT) Mice, Rag-Deficient Mice Have Large Numbers of Commensal

Question 21

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Like wild-type (WT) mice, Rag-deficient mice have large numbers of commensal microbes in their gastrointestinal (GI) tract that remain contained in restricted to anatomical locations associated with the GI tract. However, when Rag-deficient mice are treated with a depleting antibody that eliminates all lymphocytes from the animals, these mice suffer from dissemination of commensal bacteria to peripheral organs, such as spleen and liver, and show evidence of systemic inflammation as shown by cytokine levels in the serum. ND, not detected; D3, day 3 post-antibody injection; D14, day 14 post-antibody injection. Like wild-type (WT) mice, Rag-deficient mice have large numbers of commensal microbes in their gastrointestinal (GI) tract that remain contained in restricted to anatomical locations associated with the GI tract. However, when Rag-deficient mice are treated with a depleting antibody that eliminates all lymphocytes from the animals, these mice suffer from dissemination of commensal bacteria to peripheral organs, such as spleen and liver, and show evidence of systemic inflammation as shown by cytokine levels in the serum. ND, not detected; D3, day 3 post-antibody injection; D14, day 14 post-antibody injection. a) What are the cells in Rag-deficient mice, that, when depleted by the antibody injection, cause bacterial dissemination and systemic inflammation? In a follow-up study, the Rag-deficient mice were treated with a blocking antibody to neutralize a cytokine (cytokine Z) known to be produced by lymphocytes. On day 14 post-antibody injection, the spleen and liver of the mice were analyzed for numbers of bacteria, and the results are shown in Figure : b) What is the likely identity of cytokine Z? In a second follow-up study, Rag-deficient mice were crossed to a knockout for a transcription factor (Factor X) also known to be expressed in some lymphocytes. Lamina propria lymphocytes were isolated from wild-type mice, Rag-deficient mice, Factor-X-deficient mice, and double Rag/Factor-X deficient mice, and mRNA was prepared from the cells. RT-PCR was then used to determine the mRNA transcript levels for cytokine Z in all four lymphocyte populations, and the results are shown in Figure. c) What is the likely identity of Factor X? In a final experiment, the entire small intestine of wild-type mice, Rag-deficient mice, or Factor X-deficient mice is isolated and processed for mRNA, which is then used in RT-PCR experiments. Expression levels of mRNA encoding RegIII \beta and RegIII \gamma are assessed in these samples; the results are shown in Figure. d) What do these data indicate about the regulation of RegIII \beta and RegIII \gamma expression? Which cells are expressing RegIII \beta and RegIII \gamma ?
a) What are the cells in Rag-deficient mice, that, when depleted by the antibody injection, cause bacterial dissemination and systemic inflammation?
In a follow-up study, the Rag-deficient mice were treated with a blocking antibody to neutralize a cytokine (cytokine Z) known to be produced by lymphocytes. On day 14 post-antibody injection, the spleen and liver of the mice were analyzed for numbers of bacteria, and the results are shown in Figure :
Like wild-type (WT) mice, Rag-deficient mice have large numbers of commensal microbes in their gastrointestinal (GI) tract that remain contained in restricted to anatomical locations associated with the GI tract. However, when Rag-deficient mice are treated with a depleting antibody that eliminates all lymphocytes from the animals, these mice suffer from dissemination of commensal bacteria to peripheral organs, such as spleen and liver, and show evidence of systemic inflammation as shown by cytokine levels in the serum. ND, not detected; D3, day 3 post-antibody injection; D14, day 14 post-antibody injection. a) What are the cells in Rag-deficient mice, that, when depleted by the antibody injection, cause bacterial dissemination and systemic inflammation? In a follow-up study, the Rag-deficient mice were treated with a blocking antibody to neutralize a cytokine (cytokine Z) known to be produced by lymphocytes. On day 14 post-antibody injection, the spleen and liver of the mice were analyzed for numbers of bacteria, and the results are shown in Figure : b) What is the likely identity of cytokine Z? In a second follow-up study, Rag-deficient mice were crossed to a knockout for a transcription factor (Factor X) also known to be expressed in some lymphocytes. Lamina propria lymphocytes were isolated from wild-type mice, Rag-deficient mice, Factor-X-deficient mice, and double Rag/Factor-X deficient mice, and mRNA was prepared from the cells. RT-PCR was then used to determine the mRNA transcript levels for cytokine Z in all four lymphocyte populations, and the results are shown in Figure. c) What is the likely identity of Factor X? In a final experiment, the entire small intestine of wild-type mice, Rag-deficient mice, or Factor X-deficient mice is isolated and processed for mRNA, which is then used in RT-PCR experiments. Expression levels of mRNA encoding RegIII \beta and RegIII \gamma are assessed in these samples; the results are shown in Figure. d) What do these data indicate about the regulation of RegIII \beta and RegIII \gamma expression? Which cells are expressing RegIII \beta and RegIII \gamma ?
b) What is the likely identity of cytokine Z?
In a second follow-up study, Rag-deficient mice were crossed to a knockout for a transcription factor (Factor X) also known to be expressed in some lymphocytes. Lamina propria lymphocytes were isolated from wild-type mice, Rag-deficient mice, Factor-X-deficient mice, and double Rag/Factor-X deficient mice, and mRNA was prepared from the cells. RT-PCR was then used to determine the mRNA transcript levels for cytokine Z in all four lymphocyte populations, and the results are shown in Figure. Like wild-type (WT) mice, Rag-deficient mice have large numbers of commensal microbes in their gastrointestinal (GI) tract that remain contained in restricted to anatomical locations associated with the GI tract. However, when Rag-deficient mice are treated with a depleting antibody that eliminates all lymphocytes from the animals, these mice suffer from dissemination of commensal bacteria to peripheral organs, such as spleen and liver, and show evidence of systemic inflammation as shown by cytokine levels in the serum. ND, not detected; D3, day 3 post-antibody injection; D14, day 14 post-antibody injection. a) What are the cells in Rag-deficient mice, that, when depleted by the antibody injection, cause bacterial dissemination and systemic inflammation? In a follow-up study, the Rag-deficient mice were treated with a blocking antibody to neutralize a cytokine (cytokine Z) known to be produced by lymphocytes. On day 14 post-antibody injection, the spleen and liver of the mice were analyzed for numbers of bacteria, and the results are shown in Figure : b) What is the likely identity of cytokine Z? In a second follow-up study, Rag-deficient mice were crossed to a knockout for a transcription factor (Factor X) also known to be expressed in some lymphocytes. Lamina propria lymphocytes were isolated from wild-type mice, Rag-deficient mice, Factor-X-deficient mice, and double Rag/Factor-X deficient mice, and mRNA was prepared from the cells. RT-PCR was then used to determine the mRNA transcript levels for cytokine Z in all four lymphocyte populations, and the results are shown in Figure. c) What is the likely identity of Factor X? In a final experiment, the entire small intestine of wild-type mice, Rag-deficient mice, or Factor X-deficient mice is isolated and processed for mRNA, which is then used in RT-PCR experiments. Expression levels of mRNA encoding RegIII \beta and RegIII \gamma are assessed in these samples; the results are shown in Figure. d) What do these data indicate about the regulation of RegIII \beta and RegIII \gamma expression? Which cells are expressing RegIII \beta and RegIII \gamma ?
c) What is the likely identity of Factor X?
In a final experiment, the entire small intestine of wild-type mice, Rag-deficient mice, or Factor X-deficient mice is isolated and processed for mRNA, which is then used in RT-PCR experiments. Expression levels of mRNA encoding RegIII β\beta and RegIII γ\gamma are assessed in these samples; the results are shown in Figure. Like wild-type (WT) mice, Rag-deficient mice have large numbers of commensal microbes in their gastrointestinal (GI) tract that remain contained in restricted to anatomical locations associated with the GI tract. However, when Rag-deficient mice are treated with a depleting antibody that eliminates all lymphocytes from the animals, these mice suffer from dissemination of commensal bacteria to peripheral organs, such as spleen and liver, and show evidence of systemic inflammation as shown by cytokine levels in the serum. ND, not detected; D3, day 3 post-antibody injection; D14, day 14 post-antibody injection. a) What are the cells in Rag-deficient mice, that, when depleted by the antibody injection, cause bacterial dissemination and systemic inflammation? In a follow-up study, the Rag-deficient mice were treated with a blocking antibody to neutralize a cytokine (cytokine Z) known to be produced by lymphocytes. On day 14 post-antibody injection, the spleen and liver of the mice were analyzed for numbers of bacteria, and the results are shown in Figure : b) What is the likely identity of cytokine Z? In a second follow-up study, Rag-deficient mice were crossed to a knockout for a transcription factor (Factor X) also known to be expressed in some lymphocytes. Lamina propria lymphocytes were isolated from wild-type mice, Rag-deficient mice, Factor-X-deficient mice, and double Rag/Factor-X deficient mice, and mRNA was prepared from the cells. RT-PCR was then used to determine the mRNA transcript levels for cytokine Z in all four lymphocyte populations, and the results are shown in Figure. c) What is the likely identity of Factor X? In a final experiment, the entire small intestine of wild-type mice, Rag-deficient mice, or Factor X-deficient mice is isolated and processed for mRNA, which is then used in RT-PCR experiments. Expression levels of mRNA encoding RegIII \beta and RegIII \gamma are assessed in these samples; the results are shown in Figure. d) What do these data indicate about the regulation of RegIII \beta and RegIII \gamma expression? Which cells are expressing RegIII \beta and RegIII \gamma ?
d) What do these data indicate about the regulation of RegIII β\beta and RegIII γ\gamma expression? Which cells are expressing RegIII β\beta and RegIII γ\gamma ?

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a) ILC3 cells. The possible include all ...

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