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Journal articles on the topic 'Primary cell culture of bivalve'

Author: Grafiati

Published: 8 June 2024

Last updated: 31 July 2025

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1

Yoshino, T. P., U. Bickham, and C. J. Bayne. "Molluscan cells in culture: primary cell cultures and cell lines." Canadian Journal of Zoology 91, no. 6 (2013): 391–404. http://dx.doi.org/10.1139/cjz-2012-0258.

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In vitro cell culture systems from molluscs have significantly contributed to our basic understanding of complex physiological processes occurring within or between tissue-specific cells, yielding information unattainable using intact animal models. In vitro cultures of neuronal cells from gastropods show how simplified cell models can inform our understanding of complex networks in intact organisms. Primary cell cultures from marine and freshwater bivalve and gastropod species are used as biomonitors for environmental contaminants, as models for gene transfer technologies, and for studies of

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2

Potts, Robert W. A., Alejandro P. Gutierrez, Yennifer Cortés-Araya, Ross D. Houston, and Tim P. Bean. "Developments in marine invertebrate primary culture reveal novel cell morphologies in the model bivalve Crassostrea gigas." PeerJ 8 (June 1, 2020): e9180. http://dx.doi.org/10.7717/peerj.9180.

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Cell culture provides useful model systems used in a wide range of biological applications, but its utility in marine invertebrates is limited due to the lack of immortalised cell lines. Primary cell and tissue cultures are typically used but remain poorly characterised for oysters, which can cause issues with experimental consistency and reproducibility. Improvements to methods of repeatable isolation, culture, and characterisation of oyster cells and tissues are required to help address these issues. In the current study, systematic improvements have been developed to facilitate the culture

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3

Odintsova, N. A., and A. V. Khomenko. "Primary cell culture from embryos of the Japanese scallop Mizuchopecten yessoensis (Bivalvia)." Cytotechnology 6, no. 1 (1991): 49–54. http://dx.doi.org/10.1007/bf00353702.

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4

Morgan, Siân R., Laura Paletto, Benjamin Rumney, et al. "Establishment of long-term ostracod epidermal culture." In Vitro Cellular & Developmental Biology - Animal 56, no. 9 (2020): 760–72. http://dx.doi.org/10.1007/s11626-020-00508-8.

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Abstract Primary crustacean cell culture was introduced in the 1960s, but to date limited cell lines have been established. Skogsbergia lerneri is a myodocopid ostracod, which has a body enclosed within a thin, durable, transparent bivalved carapace, through which the eye can see. The epidermal layer lines the inner surface of the carapace and is responsible for carapace synthesis. The purpose of the present study was to develop an in vitro epidermal tissue and cell culture method for S. lerneri. First, an optimal environment for the viability of this epidermal tissue was ascertained, while ma

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5

Odintsova, Nelly A., Vyacheslav A. Dyachuk, and Leonid P. Nezlin. "Muscle and neuronal differentiation in primary cell culture of larval Mytilus trossulus (Mollusca: Bivalvia)." Cell and Tissue Research 339, no. 3 (2010): 625–37. http://dx.doi.org/10.1007/s00441-009-0918-3.

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6

Dessai, Shanti Nilesh. "Primary culture of mantle cells of bivalve mollusc, Paphia malabarica." In Vitro Cellular & Developmental Biology - Animal 48, no. 8 (2012): 473–77. http://dx.doi.org/10.1007/s11626-012-9538-4.

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7

Le Marrec-Croq, F., D. Glaise, C. Guguen-Guillouzo, et al. "Primary cultures of heart cells from the scallp Pecten maximus (mollusca-bivalvia)." In Vitro Cellular & Developmental Biology - Animal 35, no. 5 (1999): 289–95. http://dx.doi.org/10.1007/s11626-999-0073-x.

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8

Сhadaeva, А. А., O. S. Povolyaeva, and S. G. Yurkov. "Primary cell culture in virology." "Veterinary Medicine" Journal 23, no. 01 (2020): 51–54. http://dx.doi.org/10.30896/0042-4846.2020.23.1.51-54.

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9

Dyachuk, Vyacheslav. "Extracellular matrix is required for muscle differentiation in primary cell cultures of larval Mytilus trossulus (Mollusca: Bivalvia)." Cytotechnology 65, no. 5 (2013): 725–35. http://dx.doi.org/10.1007/s10616-013-9577-z.

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10

Hosseini Khorami, Hajar, Sophie Breton, and Annie Angers. "In vitro proliferation of Mytilus edulis male germ cell progenitors." PLOS ONE 19, no. 2 (2024): e0292205. http://dx.doi.org/10.1371/journal.pone.0292205.

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Our understanding of basic cellular processes has mostly been provided by mammalian cell culture, and by some non-mammalian vertebrate and few invertebrate cell culture models. Developing reliable culture conditions for non-model organisms is essential to allow investigation of more unusual cellular processes. Here, we investigate how cells isolated from different tissues of the marine mussel Mytilus edulis thrive and survive in vitro in the hope of establishing a suitable laboratory model for the investigation of cellular mechanisms specific to these bivalve mollusks. We found that cells diss

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11

Mizumoto, Hiroyuki, Yuji Tomaru, Yoshitake Takao, Yoko Shirai, and Keizo Nagasaki. "Diverse Responses of the Bivalve-Killing Dinoflagellate Heterocapsa circularisquama to Infection by a Single-Stranded RNA Virus." Applied and Environmental Microbiology 74, no. 10 (2008): 3105–11. http://dx.doi.org/10.1128/aem.02190-07.

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ABSTRACT Viruses are believed to be significant pathogens for phytoplankton. Usually, they infect a single algal species, and often their infection is highly strain specific. However, the detailed molecular background of the strain specificity and its ecological significance have not been sufficiently understood. Here, we investigated the temporal changes in viral RNA accumulation and virus-induced cell lysis using a bloom-forming dinoflagellate Heterocapsa circularisquama and its single-stranded RNA virus, HcRNAV. We observed at least three host response patterns to virus inoculation: sensiti

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12

Ren, Daan, and Joseph D. Miller. "Primary cell culture of suprachiasmatic nucleus." Brain Research Bulletin 61, no. 5 (2003): 547–53. http://dx.doi.org/10.1016/s0361-9230(03)00193-x.

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13

Blanco, Juan, Helena Martín, Carmen Mariño, and Araceli E. Rossignoli. "Simple Diffusion as the Mechanism of Okadaic Acid Uptake by the Mussel Digestive Gland." Toxins 11, no. 7 (2019): 395. http://dx.doi.org/10.3390/toxins11070395.

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Okadaic acid (OA) and other toxins of the diarrheic shellfish poisoning (DSP) group are accumulated and transformed mainly in many bivalves, inside the digestive gland cells. In this work the absorption of okadaic acid by those cells has been studied by supplying the toxin dissolved in water and including it in oil droplets given to primary cell cultures, and by checking if the uptake is saturable and/or energy-dependent. Okadaic acid was found to be absorbed preferentially from the dissolved phase, and the uptake from oil droplets was substantially lower. The process did not require energy an

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14

De Rosa, Salvatore, Salvatore De Caro, Carmine Iodice, Giuseppina Tommonaro, Kamen Stefanov, and Simeon Popov. "Development in primary cell culture of demosponges." Journal of Biotechnology 100, no. 2 (2003): 119–25. http://dx.doi.org/10.1016/s0168-1656(02)00252-3.

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15

WATANABE, Seiki, Youichirou ISHIKAWA, Hiromi HARA, Kei HANZAWA, and Harutaka MUKOYAMA. "A Method of Primary Cell Culture for Establishing Equine Long-Term Culture Cell Lines." Journal of Equine Science 8, no. 4 (1997): 95–99. http://dx.doi.org/10.1294/jes.8.95.

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16

Jeker, Lukas T., Mehrdad Hejazi, C. Lynne Burek, Noel R. Rose, and Patrizio Caturegli. "Mouse Thyroid Primary Culture." Biochemical and Biophysical Research Communications 257, no. 2 (1999): 511–15. http://dx.doi.org/10.1006/bbrc.1999.0468.

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17

Rajendra Prasad, Athe, T. K. Bhattacharya, R. N. Chatterjee, P. Guruvishnu, and N. Govardhana Sagar. "Standardization of Primary Hepatic Cell Culture in Chicken." International Journal of Current Microbiology and Applied Sciences 7, no. 05 (2018): 80–82. http://dx.doi.org/10.20546/ijcmas.2018.705.011.

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18

Ikeda, Yuji, and Riichi Kusuda. "Studies on primary cell culture of eel leucocytes." NIPPON SUISAN GAKKAISHI 53, no. 4 (1987): 523–27. http://dx.doi.org/10.2331/suisan.53.523.

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19

LUO, SHULI, MEI SUN, RUI JIANG, GUAN WANG, and XINYI ZHANG. "Establishment of primary mouse lung adenocarcinoma cell culture." Oncology Letters 2, no. 4 (2011): 629–32. http://dx.doi.org/10.3892/ol.2011.301.

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20

Ali, Akbar, and Donald L. Reynolds. "Primary Cell Culture of Turkey Intestinal Epithelial Cells." Avian Diseases 40, no. 1 (1996): 103. http://dx.doi.org/10.2307/1592378.

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21

Wang, Yanqiang, Wei Li, John E. Phay, et al. "Primary Cell Culture Systems for Human Thyroid Studies." Thyroid 26, no. 8 (2016): 1131–40. http://dx.doi.org/10.1089/thy.2015.0518.

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22

Sashikumar, Anu, and P. V. Desai. "Development of primary cell culture from Scylla serrata." Cytotechnology 56, no. 3 (2008): 161–69. http://dx.doi.org/10.1007/s10616-008-9152-1.

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23

Grabrucker, Andreas, Bianca Vaida, Jürgen Bockmann, and Tobias M. Boeckers. "Synaptogenesis of hippocampal neurons in primary cell culture." Cell and Tissue Research 338, no. 3 (2009): 333–41. http://dx.doi.org/10.1007/s00441-009-0881-z.

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24

Akins, Robert E., Danielle Rockwood, Karyn G. Robinson, Daniel Sandusky, John Rabolt, and Christian Pizarro. "Three-Dimensional Culture Alters Primary Cardiac Cell Phenotype." Tissue Engineering Part A 16, no. 2 (2010): 629–41. http://dx.doi.org/10.1089/ten.tea.2009.0458.

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25

Kabgani, Nazanin, and Marcus J. Moeller. "The terminator mouse: salvation for primary cell culture." Kidney International 84, no. 5 (2013): 866–68. http://dx.doi.org/10.1038/ki.2013.288.

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26

FUKUZAWA, TOSHIHIKO, STEPHANIE J. HAMER, and JOSEPH T. BAGNARA. "Extracellular Matrix Constituents and Pigment Cell Expression in Primary Cell Culture." Pigment Cell Research 5, no. 5 (1992): 224–29. http://dx.doi.org/10.1111/j.1600-0749.1992.tb00541.x.

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27

Taketani, Y., and M. Mizuno. "Hormonal regulation of endometriotic cell growth in primary cell culture system." Archives of Gynecology and Obstetrics 251, no. 3 (1992): 127–32. http://dx.doi.org/10.1007/bf02718374.

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28

Witzmann, Frank A., James W. Clack, Kevin Geiss, et al. "Proteomic evaluation of cell preparation methods in primary hepatocyte cell culture." ELECTROPHORESIS 23, no. 14 (2002): 2223. http://dx.doi.org/10.1002/1522-2683(200207)23:14<2223::aid-elps2223>3.0.co;2-d.

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29

KUBAT, B., G. REISS, and E. REALE. "Medullary collecting duct cells in primary culture." Cell Biology International Reports 14 (September 1990): 53. http://dx.doi.org/10.1016/0309-1651(90)90320-x.

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30

Gerlach, Jörg C., and Peter Neuhaus. "Culture model for primary hepatocytes." In Vitro Cellular & Developmental Biology - Animal 30, no. 10 (1994): 640–42. http://dx.doi.org/10.1007/bf02631264.

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31

Bates, Sandra R., Linda W. Gonzales, Jian-Qin Tao, Peter Rueckert, Philip L. Ballard, and Aron B. Fisher. "Recovery of rat type II cell surfactant components during primary cell culture." American Journal of Physiology-Lung Cellular and Molecular Physiology 282, no. 2 (2002): L267—L276. http://dx.doi.org/10.1152/ajplung.00227.2001.

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A culture system designed to maintain the differentiated characteristics of rat type II cells based on protocols used for human fetal lung pneumocytes was investigated. Type II cells were isolated either from adult rats with elastase (adult type II cells) or from young rats (4–11 days postnatal) with collagenase and trypsin (young type II cells) and were incubated with dexamethasone (Dex, 10 nM) and cAMP (0.1 mM). By day 4 of culture with hormone treatment, the mRNA levels in adult type II cells were less than 3% of day 0 values, whereas surfactant protein (SP)-A protein content was 26%. Howev

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32

González-Pazmiño, José, Krizia Maribell Pretell, Karina Zapata-Vidaurre, Maribel Lucero Mesones, Juan Quimí-Mujica, and Benoit Diringer. "Microbial characterization of a natural biofilm associated with Peruvian scallop (Argopecten purpuratus) larvae settlement on artificial collector by confocal imaging, microbiology, and metagenomic analysis." Latin American Journal of Aquatic Research 49, no. 1 (2021): 86–96. http://dx.doi.org/10.3856/vol49-issue1-fulltext-2547.

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Biofilms strongly influence bivalve settlement patterns on artificial substrates; however, their structure and taxonomic composition remains a black box. We characterized a natural biofilm composition that exhibits a large settlement of larvae of the Peruvian scallop Argopecten purpuratus by culture-dependent and culture-independent methods. Thirty-two different strains, representing six genera (10 strains of Bacillus, 9 of Vibrio, 6 Acinetobacter, 4 Staphylococcus, 2 Photobacterium, and 1 Exiguobacterium) were isolated. Those strains represented only 1.09% of the relative abundance compared w

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33

Karalyan, Zaven, Lusine Simonyan, Alla Misakyan, et al. "Cell Development in Primary Culture of Porcine Bone Marrow." CellBio 03, no. 02 (2014): 43–49. http://dx.doi.org/10.4236/cellbio.2014.32005.

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34

Hellermann, Gary R. "Book Review: A Manual for Primary Human Cell Culture." Cell Transplantation 14, no. 10 (2005): 859–60. http://dx.doi.org/10.3727/000000005783982585.

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35

Alamri, Ahmad M., Keunsoo Kang, Svenja Groeneveld, et al. "Primary cancer cell culture: mammary-optimized vs conditional reprogramming." Endocrine-Related Cancer 23, no. 7 (2016): 535–54. http://dx.doi.org/10.1530/erc-16-0071.

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The impact of different culture conditions on biology of primary cancer cells is not always addressed. Here, conditional reprogramming (CRC) was compared with mammary-optimized EpiCult-B (EpiC) for primary mammary epithelial cell isolation and propagation, allograft generation, and genome-wide transcriptional consequences using cancer and non-cancer mammary tissue from mice with different dosages of Brca1 and p53. Selective comparison to DMEM was included. Primary cultures were established with all three media, but CRC was most efficient for initial isolation (P<0.05). Allograft development

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36

Forrest, I. A. "Primary airway epithelial cell culture from lung transplant recipients." European Respiratory Journal 26, no. 6 (2005): 1080–85. http://dx.doi.org/10.1183/09031936.05.00141404.

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37

CALKINS, J. H., M. M. SIGEL, H. R. NANKIN, and T. LIN. "Interleukin-1 Inhibits Leydig Cell Steroidogenesis in Primary Culture*." Endocrinology 123, no. 3 (1988): 1605–10. http://dx.doi.org/10.1210/endo-123-3-1605.

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38

Fernandes, M. N., F. B. Eddy, and W. S. Penrice. "Primary cell culture from gill explants of rainbow trout." Journal of Fish Biology 47, no. 4 (1995): 641–51. http://dx.doi.org/10.1111/j.1095-8649.1995.tb01931.x.

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39

Hagiwara, Yasuko, and Eijiro Ozawa. "Effects of hydroxyurea in primary skeletal muscle cell culture." Japanese Journal of Pharmacology 61 (1993): 203. http://dx.doi.org/10.1016/s0021-5198(19)51687-0.

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40

Sheridan, Robert E., Theresa J. Smith, and Michael Adler. "Primary cell culture for evaluation of botulinum neurotoxin antagonists." Toxicon 45, no. 3 (2005): 377–82. http://dx.doi.org/10.1016/j.toxicon.2004.11.009.

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41

Leung, K. W., Y. S. Chan, and K. K. L. Yung. "Dichlorodiphenyltrichloroethane Specifically Depletes Dopaminergic Neurons in Primary Cell Culture." Neuroembryology and Aging 2, no. 3 (2003): 95–102. http://dx.doi.org/10.1159/000074188.

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42

Yurdakök-Dikmen, Begüm, Pınar Arslan, Özgür Kuzukıran, Ayhan Filazi, and Figen Erkoç. "Unio sp. primary cell culture potential in ecotoxicology research." Toxin Reviews 37, no. 1 (2017): 75–81. http://dx.doi.org/10.1080/15569543.2017.1331360.

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43

Kim, Sooah, Byung Woo Kim, Vicky P. Prizmic, et al. "Simple cell culture media expansion of primary mouse keratinocytes." Journal of Dermatological Science 93, no. 2 (2019): 135–38. http://dx.doi.org/10.1016/j.jdermsci.2018.12.002.

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44

Ju, Hyunhee, and Sungho Ghil. "Primary cell culture method for the honeybee Apis mellifera." In Vitro Cellular & Developmental Biology - Animal 51, no. 9 (2015): 890–93. http://dx.doi.org/10.1007/s11626-015-9924-9.

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45

Payushina, O. V., N. N. Butorina, O. N. Sheveleva, M. N. Kozhevnikova, and V. I. Starostin. "Cell Composition of the Primary Culture of Fetal Liver." Bulletin of Experimental Biology and Medicine 154, no. 4 (2013): 566–73. http://dx.doi.org/10.1007/s10517-013-2001-z.

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46

Walpita, Deepika, and Bridget K. Wagner. "Evaluation of Compounds in Primary Human Islet Cell Culture." Current Protocols in Chemical Biology 6, no. 3 (2014): 157–68. http://dx.doi.org/10.1002/9780470559277.ch140088.

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47

Michel, Olga, Piotr Błasiak, Jolanta Saczko, Julita Kulbacka, Małgorzata Drąg‐Zalesińska, and Adam Rzechonek. "Electropermeabilization of metastatic chondrosarcoma cells from primary cell culture." Biotechnology and Applied Biochemistry 66, no. 6 (2019): 945–54. http://dx.doi.org/10.1002/bab.1809.

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48

Bermudez-Lekerika, Paola, Katherine B. Crump, Karin Wuertz-Kozak, Christine L. Le Maitre, and Benjamin Gantenbein. "Sulfated Hydrogels as Primary Intervertebral Disc Cell Culture Systems." Gels 10, no. 5 (2024): 330. http://dx.doi.org/10.3390/gels10050330.

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The negatively charged extracellular matrix plays a vital role in intervertebral disc tissues, providing specific cues for cell maintenance and tissue hydration. Unfortunately, suitable biomimetics for intervertebral disc regeneration are lacking. Here, sulfated alginate was investigated as a 3D culture material due to its similarity to the charged matrix of the intervertebral disc. Precursor solutions of standard alginate, or alginate with 0.1% or 0.2% degrees of sulfation, were mixed with primary human nucleus pulposus cells, cast, and cultured for 14 days. A 0.2% degree of sulfation resulte

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49

He, Lingjie, Cheng Zhao, Qi Xiao, et al. "Profiling the Physiological Roles in Fish Primary Cell Culture." Biology 12, no. 12 (2023): 1454. http://dx.doi.org/10.3390/biology12121454.

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Fish primary cell culture has emerged as a valuable tool for investigating the physiological roles and responses of various cell types found in fish species. This review aims to provide an overview of the advancements and applications of fish primary cell culture techniques, focusing on the profiling of physiological roles exhibited by fish cells in vitro. Fish primary cell culture involves the isolation and cultivation of cells directly derived from fish tissues, maintaining their functional characteristics and enabling researchers to study their behavior and responses under controlled condit

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50

Demchenko, A. G., and S. A. Smirnikhina. "Ciliated cell cultures for diagnosis of primary ciliary dyskinesia." PULMONOLOGIYA 33, no. 2 (2023): 210–15. http://dx.doi.org/10.18093/0869-0189-2023-33-2-210-215.

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Primary ciliary dyskinesia (PCD) is a hereditary autosomal recessive disease that results in a defect in the ultrastructure of epithelial cilia. To date, there is no single diagnostic test for PCD, so the diagnosis is based on the results of multiple tests, such as DNA diagnostics, assessment of nasal nitric oxide levels, ciliary beat frequency (CBF) in nasal biopsy, ciliary ultrastructure, etc. Diagnosis of PCD can be difficult due to secondary damage to the airway epithelium, leading to undiagnosed or false positive cases.The aim of this work was to review studies on the cultivation of human

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