Division of Hand, Plastic and Aesthetic Surgery, LMU University Hospital, LMU Munich, 80336 Munich, Germany.
Molecular Plant Science, Department Biology I, LMU Munich, 80336 Munich, Germany.
Int J Mol Sci. 2024 Mar 31;25(7):3922. doi: 10.3390/ijms25073922.
Being the green gold of the future, cyanobacteria have recently attracted considerable interest worldwide. This study investigates the adaptability and biocompatibility of the cyanobacterial strain sp. PCC 7002 with human dermal cells, focusing on its potential application in biomedical contexts. First, we investigated the adaptability of PCC 7002 bacteria to human cell culture conditions. Next, we evaluated the biocompatibility of cyanobacteria with common dermal cells, like 3T3 fibroblasts and HaCaT keratinocytes. Therefore, cells were directly and indirectly cocultured with the corresponding cells, and we measured metabolic activity (AlamarBlue assay) and proliferation (cell count and PicoGreen assay). The lactate dehydrogenase (LDH) assay was performed to determine the cytotoxic effect of cyanobacteria and their nutrition medium on human dermal cells. The cyanobacteria exhibited exponential growth under conventional human cell culture conditions, with the temperature and medium composition not affecting their viability. In addition, the effect of illumination on the proliferation capacity was investigated, showing a significant impact of light exposure on bacterial growth. The measured oxygen production under hypoxic conditions demonstrated a sufficient oxygen supply for further tissue engineering approaches depending on the number of bacteria. There were no significant adverse effects on human cell viability and growth under coculture conditions, whereas the LDH assay assessed signs of cytotoxicity regarding 3T3 fibroblasts after 2 days of coculturing. These negative effects were dismissed after 4 days. The findings highlight the potential of sp. PCC 7002 for integration into biomedical approaches. We found no cytotoxicity of cyanobacteria on 3T3 fibroblasts and HaCaT keratinocytes, thus paving the way for further in vivo studies to assess long-term effects and systemic reactions.
作为未来的绿色黄金,蓝细菌最近在全球范围内引起了相当大的关注。本研究调查了蓝细菌株 sp. PCC 7002 与人真皮细胞的适应性和生物相容性,重点关注其在生物医学背景下的潜在应用。首先,我们研究了 PCC 7002 细菌对人类细胞培养条件的适应性。接下来,我们评估了蓝细菌与常见真皮细胞(如 3T3 成纤维细胞和 HaCaT 角质形成细胞)的生物相容性。因此,细胞直接和间接与相应的细胞共培养,并测量代谢活性(AlamarBlue 测定)和增殖(细胞计数和 PicoGreen 测定)。通过乳酸脱氢酶(LDH)测定来确定蓝细菌及其营养培养基对人真皮细胞的细胞毒性作用。蓝细菌在常规人类细胞培养条件下呈指数生长,温度和培养基组成不影响其活力。此外,还研究了光照对增殖能力的影响,结果表明光照对细菌生长有显著影响。在低氧条件下测量的产氧量表明,根据细菌数量,可以为进一步的组织工程方法提供充足的氧气供应。在共培养条件下,对人真皮细胞活力和生长没有明显的不良影响,而 LDH 测定在共培养 2 天后评估了对 3T3 成纤维细胞的细胞毒性迹象。这些负面影响在 4 天后消失。这些发现突出了 sp. PCC 7002 整合到生物医学方法中的潜力。我们没有发现蓝细菌对 3T3 成纤维细胞和 HaCaT 角质形成细胞的细胞毒性,从而为进一步的体内研究铺平了道路,以评估长期影响和全身反应。