Centre for Bioinnovation, University of the Sunshine Coast (UniSC), 4 Locked Bag, Maroochydore, QLD 4558, Australia.
School of Science, Technology and Engineering, University of the Sunshine Coast (UniSC), 4 Locked Bag, Maroochydore, QLD 4558, Australia.
Int J Mol Sci. 2024 Aug 7;25(16):8623. doi: 10.3390/ijms25168623.
In the face of rising global demand and unsustainable production methods, cultivated crustacean meat (CCM) is proposed as an alternative means to produce delicious lobster, shrimp, and crab products. Cultivated meat requires starting stem cells that may vary in terms of potency and the propensity to proliferate or differentiate into myogenic (muscle-related) tissues. Recognizing that regenerating limbs are a non-lethal source of tissue and may harbor relevant stem cells, we selected those of the crayfish as our model. To investigate stem cell activity, we conducted RNA-Seq analysis across six stages of claw regeneration (four pre-molt and two post-molt stages), along with histology and real-time quantitative PCR (qPCR). Our results showed that while genes related to energy production, muscle hypertrophy, and exoskeletal cuticle synthesis dominated the post-molt stages, growth factor receptors (FGFR, EGFR, TGFR, and BMPR) and those related to stem cell proliferation and potency (Cyclins, CDKs, Wnts, C-Myc, Klf4, Sox2, PCNA, and p53) were upregulated before the molt. Pre-molt upregulation in several genes occurred in two growth peaks; Stages 2 and 4. We therefore propose that pre-molt limb regeneration tissues, particularly those in the larger Stage 4, present a prolific and non-lethal source of stem cells for CCM development.
面对全球需求的增长和不可持续的生产方式,养殖甲壳类肉(CCM)被提议作为生产美味龙虾、虾和蟹类产品的替代方法。养殖肉需要起始干细胞,这些干细胞在效力和增殖或分化为肌源性(与肌肉相关)组织的倾向方面可能有所不同。认识到再生肢体是一种非致命的组织来源,并且可能含有相关的干细胞,我们选择了小龙虾的肢体作为我们的模型。为了研究干细胞的活性,我们对爪子再生的六个阶段(四个蜕皮前和两个蜕皮后阶段)进行了 RNA-Seq 分析,同时进行了组织学和实时定量 PCR(qPCR)分析。我们的结果表明,虽然与能量产生、肌肉肥大和外骨骼甲壳质合成相关的基因在蜕皮后阶段占主导地位,但生长因子受体(FGFR、EGFR、TGFR 和 BMPR)以及与干细胞增殖和效力相关的基因(细胞周期蛋白、CDKs、Wnts、C-Myc、Klf4、Sox2、PCNA 和 p53)在蜕皮前就被上调了。几个基因在两个生长高峰期(第 2 阶段和第 4 阶段)都有前蜕皮期的上调。因此,我们提出前蜕皮期肢体再生组织,特别是较大的第 4 阶段的组织,是 CCM 开发的丰富且非致命的干细胞来源。