CIRM Bridges 2.0: Training the Next Generation of Stem Cell Scientists
Grant Award Details
Grant Type:
Grant Number:
EDUC2-08391
Investigator(s):
Award Value:
$2,958,876
Status:
Closed
Progress Reports
Reporting Period:
Year 1
Reporting Period:
Year 2
Reporting Period:
Year 3
Reporting Period:
Year 4
Reporting Period:
Year 5 Supplemental
Grant Application Details
Application Title:
CIRM Bridges 2.0: Training the Next Generation of Stem Cell Scientists
Public Abstract:
We are a large, urban university serving a highly diverse student population. Our proposed program would support 10 master’s-level trainees annually from two different master’s program in Biology: a Masters of Science in Cell and Molecular Biology with an emphasis in Stem Cell Biology (the “MS program”) and a Professional Science Masters with a concentration in Stem Cell Science (the “PSM program”). The PSM program provides additional course work in business and is tailored towards students interested in pursuing a position in the biotechnology sector upon graduation. In the first year of the program, CIRM Bridges trainees take core courses to build a strong foundation in stem cell science. In addition, two additional graduate courses that are complementary to the CIRM Bridges 2.0 mission will be included as part of this curriculum; “Careers in Life Sciences”, which will help guide students in entering the Life Sciences job market and “Biomedical Product Development & Regulations”, which provides students with an understanding of the process involved in product development with a special focus on stem cell therapies. After completing the first-year course work, students will participate in a week-long intensive Stem Cell Laboratory course taught by faculty at one of the host sites where they will learn to propagate, maintain, and manipulate human stem cells. By the second year, all of the CIRM Bridges trainees will have joined a stem cell research lab at one of our host institutions or affiliated stem cell companies. All CIRM trainees will conduct research using human stem cells. At the end of their second year of training, trainees will complete a final master project report written in the form of a manuscript as well as an oral thesis defense. This effective training has successfully led to 29 publications by CIRM Bridges trainees in peer-reviewed journals. Mentoring and professional development are an integral part of the CIRM Bridges program. CIRM students will attend monthly meetings with the Program Director (PD) to cover a range of topics as well meet alumni, industry and academic stem cell scientists. Students will also gain a broader introduction to the importance and application of stem cell research from guest speakers, including members of various patient advocate groups. The PD and Program Associate will meet regularly with the students and their research mentors to provide continuity of programming and ensure that students thrive in their internships. Thus, the proposed program aims to make important contributions to the development of a talented and diverse pool of trained professionals that will help advance CIRM’s mission to develop stem cell therapies to meet the medical needs of our state and nation.
Statement of Benefit to California:
The proposed CIRM Bridges program will benefit the state of California and its residents by providing training to prepare students to enter research careers in stem cell biology and regenerative medicine. This is particularly important and timely because our state is positioned to become a leader in stem cell research and product development both nationally and globally. With this growing field it will be crucial to have skilled professionals equipped to meet the scientific and technical challenges necessary for advancing this field. We are extremely well situated to contribute to this effort. Thus far, 62 students have completed this training program since 2009. Of these students, 56% are working as research associates in biotech or in academic labs, while 21% have entered prestigious PhD programs, and 13% have enter medically-oriented training program. Of the students that received CIRM fellowships, 60% are underrepresented minorities and 51% are women. Thus, the program has been successful in training a high caliber and diverse stem cell workforce ready for the scientific challenges that lay ahead. The CIRM Bridges program, along with other training programs in our college, have played an important role in establishing our national reputation for contributing to the diversification of the biomedical profession ready to meet the needs of an increasingly diverse society.
With the help of our partnering research institutions, our CIRM Bridges program will provides cutting edge lab and lecture courses, research internships, professional mentoring, and community service opportunities to ensure that our students possess not only scientific and technical proficiency but have a thorough grasp of the ethical implications of the technology and the ability to communicate effectively with a general as well as a scientific audience. The research internships will provide training in laboratories of premiere research institutions at the forefront of stem cell research. Students completing this program will have the knowledge, skills and experience necessary to work with both federally and non-federally registered human stem cell lines. We will also offer two new biotechnology courses that will provide students with a better understanding of how stem-cell based therapies reach the market as well as a broader understanding of the life science career paths. Our graduates will be fully prepared to contribute to the growth of a vibrant stem cell industry that is aware of the challenges and diverse needs of the patients in our state.
Publications
- Cell Rep (2014): Activation of neuronal gene expression by the JMJD3 demethylase is required for postnatal and adult brain neurogenesis. (PubMed: 25176653)
- Dev Cell (2017): Alternative Progenitor Cells Compensate to Rebuild the Coronary Vasculature in Elabela- and Apj-Deficient Hearts. (PubMed: 28890073)
- Environ Health (2020): Association of polybrominated diphenyl ether (PBDE) levels with biomarkers of placental development and disease during mid-gestation. (PubMed: 32493340)
- Curr HIV/AIDS Rep (2020): From Berlin to London: HIV-1 Reservoir Reduction Following Stem Cell Transplantation. (PubMed: 32519184)
- Bone Marrow Transplant (2021): A bioinspired and chemically defined alternative to dimethyl sulfoxide for the cryopreservation of human hematopoietic stem cells. (PubMed: 34155359)
- Cell (2022): Cannabinoid receptor 1 antagonist genistein attenuates marijuana-induced vascular inflammation. (PubMed: 35489334)
- Cells (2021): Characterization and Biomarker Analyses of Post-COVID-19 Complications and Neurological Manifestations. (PubMed: 33668514)
- Stem Cells (2016): Comprehensive Proteomic Analysis of Mesenchymal Stem Cell Exosomes Reveals Modulation of Angiogenesis via Nuclear Factor-KappaB Signaling. (PubMed: 26782178)
- Science (2019): CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiency. (PubMed: 30545847)
- Elife (2020): Delineating the early transcriptional specification of the mammalian trachea and esophagus. (PubMed: 32515350)
- Open Forum Infect Dis (2021): Discordant Virus-Specific Antibody Levels, Antibody Neutralization Capacity, and T-cell Responses Following 3 Doses of SARS-CoV-2 Vaccination in a Patient With Connective Tissue Disease. (PubMed: 34395717)
- Hepatology (2021): Doxycycline Significantly Enhances Induction of Induced Pluripotent Stem Cells to Endoderm by Enhancing Survival Through Protein Kinase B Phosphorylation. (PubMed: 33982322)
- Nature (2021): Early-life inflammation primes a T helper 2 cell-fibroblast niche in skin. (PubMed: 34707292)
- Science (2016): Extensive migration of young neurons into the infant human frontal lobe. (PubMed: 27846470)
- J Vis Exp (2021): Fabrication of 3D Cardiac Microtissue Arrays using Human iPSC-Derived Cardiomyocytes, Cardiac Fibroblasts, and Endothelial Cells. (PubMed: 33779590)
- Cell Stem Cell (2018): FOXD3 Regulates Pluripotent Stem Cell Potential by Simultaneously Initiating and Repressing Enhancer Activity. (PubMed: 30075131)
- Nat Protoc (2017): Generation and use of a humanized bone-marrow-ossicle niche for hematopoietic xenotransplantation into mice. (PubMed: 28933777)
- Toxicol Sci (2019): Genomic Profiling of BDE-47 Effects on Human Placental Cytotrophoblasts. (PubMed: 30202865)
- Development (2021): Global proteomic analyses of human cytotrophoblast differentiation/invasion. (PubMed: 34121116)
- Cell Genom (2022): High-throughput characterization of the role of non-B DNA motifs on promoter function. (PubMed: 35573091)
- Cell Stem Cell (2015): The long noncoding RNA pnky regulates neuronal differentiation of embryonic and postnatal neural stem cells. (PubMed: 25800779)
- Transl Res (2021): LONG-TERM IMMUNOLOGIC EFFECTS OF SARS-CoV-2 INFECTION: LEVERAGING TRANSLATIONAL RESEARCH METHODOLOGY TO ADDRESS EMERGING QUESTIONS. (PubMed: 34780969)
- Cell Rep (2021): Long-term SARS-CoV-2-specific immune and inflammatory responses in individuals recovering from COVID-19 with and without post-acute symptoms. (PubMed: 34358460)
- Circulation (2022): Modeling Effects of Immunosuppressive Drugs on Human Hearts Using Induced Pluripotent Stem Cell-Derived Cardiac Organoids and Single-Cell RNA Sequencing. (PubMed: 35467958)
- Elife (2017): Multiplexed genetic engineering of human hematopoietic stem and progenitor cells using CRISPR/Cas9 and AAV6. (PubMed: 28956530)
- Genome Res (2016): A new class of temporarily phenotypic enhancers identified by CRISPR/Cas9-mediated genetic screening. (PubMed: 26813977)
- Toxicol Sci (2021): Organophosphate Flame Retardants, Highly Fluorinated Chemicals, and Biomarkers of Placental Development and Disease During Mid-Gestation. (PubMed: 33677611)
- Prenat Diagn (2016): Placental transcriptomes in the common aneuploidies reveal critical regions on the trisomic chromosomes and genome-wide effects. (PubMed: 27328057)
- Elife (2017): Resolving stem and progenitor cells in the adult mouse incisor through gene co-expression analysis. (PubMed: 28475038)
- Nat Commun (2017): Systematic discovery of mutation-specific synthetic lethals by mining pan-cancer human primary tumor data. (PubMed: 28561042)
- Sci Transl Med (2022): Treatment of a genetic brain disease by CNS-wide microglia replacement. (PubMed: 35294256)
- Mol Autism (2018): The valproic acid rat model of autism presents with gut bacterial dysbiosis similar to that in human autism. (PubMed: 30555669)