Transplantation of Adipose-Tissue-Engineered Constructs with CRISPR-Mediated UCP1 Activation
Thermogenic adipocytes have potential utility for the development of approaches to treat type 2 diabetes and obesity-associated diseases. Although several reports have proved the positive effect of beige and brown adipocyte transplantation in obese mice, translation to human cell therapy needs impro...
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Published in | International journal of molecular sciences Vol. 24; no. 4; p. 3844 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Thermogenic adipocytes have potential utility for the development of approaches to treat type 2 diabetes and obesity-associated diseases. Although several reports have proved the positive effect of beige and brown adipocyte transplantation in obese mice, translation to human cell therapy needs improvement. Here, we describe the application of CRISPR activation (CRISPRa) technology for generating safe and efficient adipose-tissue-engineered constructs with enhanced mitochondrial uncoupling protein 1 (UCP1) expression. We designed the CRISPRa system for the activation of UCP1 gene expression. CRISPRa-UCP1 was delivered into mature adipocytes by a baculovirus vector. Modified adipocytes were transplanted in C57BL/6 mice, followed by analysis of grafts, inflammation and systemic glucose metabolism. Staining of grafts on day 8 after transplantation shows them to contain UCP1-positive adipocytes. Following transplantation, adipocytes remain in grafts and exhibit expression of PGC1α transcription factor and hormone sensitive lipase (HSL). Transplantation of CRISPRa-UCP1-modified adipocytes does not influence glucose metabolism or inflammation in recipient mice. We show the utility and safety of baculovirus vectors for CRISPRa-based thermogenic gene activation. Our findings suggest a means of improving existing cell therapy approaches using baculovirus vectors and CRISPRa for modification and transplantation of non-immunogenic adipocytes. |
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AbstractList | Thermogenic adipocytes have potential utility for the development of approaches to treat type 2 diabetes and obesity-associated diseases. Although several reports have proved the positive effect of beige and brown adipocyte transplantation in obese mice, translation to human cell therapy needs improvement. Here, we describe the application of CRISPR activation (CRISPRa) technology for generating safe and efficient adipose-tissue-engineered constructs with enhanced mitochondrial uncoupling protein 1 (UCP1) expression. We designed the CRISPRa system for the activation of UCP1 gene expression. CRISPRa-UCP1 was delivered into mature adipocytes by a baculovirus vector. Modified adipocytes were transplanted in C57BL/6 mice, followed by analysis of grafts, inflammation and systemic glucose metabolism. Staining of grafts on day 8 after transplantation shows them to contain UCP1-positive adipocytes. Following transplantation, adipocytes remain in grafts and exhibit expression of PGC1α transcription factor and hormone sensitive lipase (HSL). Transplantation of CRISPRa-UCP1-modified adipocytes does not influence glucose metabolism or inflammation in recipient mice. We show the utility and safety of baculovirus vectors for CRISPRa-based thermogenic gene activation. Our findings suggest a means of improving existing cell therapy approaches using baculovirus vectors and CRISPRa for modification and transplantation of non-immunogenic adipocytes.Thermogenic adipocytes have potential utility for the development of approaches to treat type 2 diabetes and obesity-associated diseases. Although several reports have proved the positive effect of beige and brown adipocyte transplantation in obese mice, translation to human cell therapy needs improvement. Here, we describe the application of CRISPR activation (CRISPRa) technology for generating safe and efficient adipose-tissue-engineered constructs with enhanced mitochondrial uncoupling protein 1 (UCP1) expression. We designed the CRISPRa system for the activation of UCP1 gene expression. CRISPRa-UCP1 was delivered into mature adipocytes by a baculovirus vector. Modified adipocytes were transplanted in C57BL/6 mice, followed by analysis of grafts, inflammation and systemic glucose metabolism. Staining of grafts on day 8 after transplantation shows them to contain UCP1-positive adipocytes. Following transplantation, adipocytes remain in grafts and exhibit expression of PGC1α transcription factor and hormone sensitive lipase (HSL). Transplantation of CRISPRa-UCP1-modified adipocytes does not influence glucose metabolism or inflammation in recipient mice. We show the utility and safety of baculovirus vectors for CRISPRa-based thermogenic gene activation. Our findings suggest a means of improving existing cell therapy approaches using baculovirus vectors and CRISPRa for modification and transplantation of non-immunogenic adipocytes. Thermogenic adipocytes have potential utility for the development of approaches to treat type 2 diabetes and obesity-associated diseases. Although several reports have proved the positive effect of beige and brown adipocyte transplantation in obese mice, translation to human cell therapy needs improvement. Here, we describe the application of CRISPR activation (CRISPRa) technology for generating safe and efficient adipose-tissue-engineered constructs with enhanced mitochondrial uncoupling protein 1 (UCP1) expression. We designed the CRISPRa system for the activation of UCP1 gene expression. CRISPRa-UCP1 was delivered into mature adipocytes by a baculovirus vector. Modified adipocytes were transplanted in C57BL/6 mice, followed by analysis of grafts, inflammation and systemic glucose metabolism. Staining of grafts on day 8 after transplantation shows them to contain UCP1-positive adipocytes. Following transplantation, adipocytes remain in grafts and exhibit expression of PGC1α transcription factor and hormone sensitive lipase (HSL). Transplantation of CRISPRa-UCP1-modified adipocytes does not influence glucose metabolism or inflammation in recipient mice. We show the utility and safety of baculovirus vectors for CRISPRa-based thermogenic gene activation. Our findings suggest a means of improving existing cell therapy approaches using baculovirus vectors and CRISPRa for modification and transplantation of non-immunogenic adipocytes. |
Audience | Academic |
Author | Stafeev, Iurii Truong, Vu Anh Michurina, Svetlana Ratner, Elizaveta Hu, Yu-Chen Boldyreva, Maria Menshikov, Mikhail Parfyonova, Yelena |
AuthorAffiliation | 4 Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300044, Taiwan 3 Cell and Molecular Biology Unit, Faculty of Biology and Biotechnology, National Research University Higher School of Economics, 101000 Moscow, Russia 1 National Medical Research Centre of Cardiology Named after Academician E. I. Chazov, 121552 Moscow, Russia 5 Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University, Hsinchu 300044, Taiwan 2 Faculty of Biology, Lomonosov Moscow State University, 119991 Moscow, Russia 6 Faculty of Basic Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia |
AuthorAffiliation_xml | – name: 3 Cell and Molecular Biology Unit, Faculty of Biology and Biotechnology, National Research University Higher School of Economics, 101000 Moscow, Russia – name: 2 Faculty of Biology, Lomonosov Moscow State University, 119991 Moscow, Russia – name: 6 Faculty of Basic Medicine, Lomonosov Moscow State University, 119991 Moscow, Russia – name: 5 Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University, Hsinchu 300044, Taiwan – name: 1 National Medical Research Centre of Cardiology Named after Academician E. I. Chazov, 121552 Moscow, Russia – name: 4 Department of Chemical Engineering, National Tsing Hua University, Hsinchu 300044, Taiwan |
Author_xml | – sequence: 1 givenname: Svetlana surname: Michurina fullname: Michurina, Svetlana – sequence: 2 givenname: Iurii surname: Stafeev fullname: Stafeev, Iurii – sequence: 3 givenname: Maria orcidid: 0000-0002-8309-0018 surname: Boldyreva fullname: Boldyreva, Maria – sequence: 4 givenname: Vu Anh orcidid: 0000-0002-8120-8684 surname: Truong fullname: Truong, Vu Anh – sequence: 5 givenname: Elizaveta surname: Ratner fullname: Ratner, Elizaveta – sequence: 6 givenname: Mikhail surname: Menshikov fullname: Menshikov, Mikhail – sequence: 7 givenname: Yu-Chen surname: Hu fullname: Hu, Yu-Chen – sequence: 8 givenname: Yelena surname: Parfyonova fullname: Parfyonova, Yelena |
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SubjectTerms | Adipocytes Adipocytes, Brown - metabolism Adipose Tissue, Brown - transplantation Adipose tissues Analysis Animals Body fat Cells Clustered Regularly Interspaced Short Palindromic Repeats CRISPR Diabetes Mellitus, Type 2 - therapy Efficiency Energy consumption Energy dissipation Gene expression Genes Genetic engineering Genomes Glucose Glucose - metabolism Humans Inflammation Metabolism Mice Mice, Inbred C57BL Morphology Obesity Scientific equipment and supplies industry Technology application Thermogenesis Thermogenesis - genetics Tissue engineering Type 2 diabetes Uncoupling Protein 1 - metabolism |
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